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Stem Cell Of America – Breakthrough Stem Cell Treatments …

Posted: October 8, 2017 at 3:50 am

Treatment

The Stem Cell treatment performed at our clinics is a painless medical procedure where Stem Cells (cellular building blocks) are usually administered intravenously and subcutaneously (under the skin). The whole procedure takes approximately one hour and has no known negative side effects.

Following the treatment, the Fetal Stem Cells will travel throughout the body, detecting damaged cells and tissue and attempts to restore them. The Fetal Stem Cells can also stimulate existing normal cells and tissues to operate at a higher level of function, boosting the bodys own repair mechanisms to aid in the healing process. These highly adaptive cells then remain in the body, continually locating and repairing any damage they encounter.

As with any medical treatment, safety should be of the highest priority. The Stem Cells used in our treatment undergo extensive screening for possible infection and impurities.

Utilizing tests more sophisticated than those regularly used in the United States for Stem Cell research and transplant. Our testing process ensures we use only the healthiest cells to enable the safest and most effective Fetal Stem Cell treatment possible. And, unlike other types of Stem Cells, there is no danger of the bodys rejection of Fetal Stem Cells due to the fact they are immune privileged. This means that you can give the cells to any patient without matching, use of immunosuppressive drugs and without rejection. This unique quality eliminates the need for drugs used to suppress the immune system, which can leave a patient exposed to serious infections.

With over 4,000 patients treated, Stem Cell Of America has achieved positive results with a wide variety of illnesses, conditions and injuries. Often, in cases where the diseases continued to worsen, our patients have reported substantial improvements following the Stem Cell treatment.

Patients have experienced favorable developments such as reduction or elimination of pain, increased strength and mobility, improved cognitive function, higher tolerance for chemotherapy, and quicker healing and recovery.

To view follow up letters from patients, please visit the patient experiences page on our website.

All statements, opinions, and advice on this page is provided for educational information only. It is not a substitute for proper medical diagnosis and care. Like all medical treatments and procedures, results may significantly vary and positive results may not always be achieved. Please contact us so we may evaluate your specific case.

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Meetings

Posted: October 8, 2017 at 3:49 am

Stem Cell Biology

September 25 - 29, 2017

Abstract Deadline: July 28, 2017

Organizers:

The meeting will focus on the basic biology of stem cells and the dynamic interactions between stem cells and their microenvironment or niche. Topics will include the mechanisms controlling stem cell proliferation, differentiation, pluripotency and reprogramming. Emerging concepts about the regulation of multipotent cells during early embryo development, tissue regeneration and tumor progression will be emphasized.

Topics:

Keynote Speaker:

Irving Weissman, Stanford University

Confirmed Discussion Leaders:

Salvador Aznar Benitah, Institute for Research in Biomedicine, SpainKristin Baldwin, The Scripps Research InstitutePhilip Beachy, Stanford UniversityHongkui Deng, Peking University, ChinaGiacomo Donati, University of Turin, ItalyValentina Greco, Yale University School of MedicineKonrad Hochedlinger, Harvard Medical SchoolBrigid Hogan, Duke University Medical CenterMeritxell Huch, University of Cambridge, UKAllon Klein, Harvard Medical SchoolChris Lengner, University of PennsylvaniaSally Lowell, MRC Centre for Regenerative Medicine, UKEmmanuelle Passegue, Columbia University Medical CenterKathrin Plath, University of California, Los AngelesJayaraj Rajagopal, Massachusetts General HospitalKristy Red-Horse, Stanford UniversityHongjun Song, Johns Hopkins UniversityBen Stanger, University of Pennsylvania, Perelman School of MedicineKiku Tachibana-Konwalski, IMBA/Institute of Molecular Biotechnology, AustriaMagdalena Zernicka-Goetz, University of Cambridge, UKYi Zhang, Harvard Medical School

Please bring this notice to the attention of any of your colleagues who may be interested in participating in the meeting.

All abstracts must be submitted by the abstract deadline. Late registrations may be accepted after the abstract deadline if the meeting is not oversubscribed. In the event of over-subscription, every effort will be made to ensure that all groups who wish to participate will be represented. The status (talk/poster) of abstracts will be posted on our web site as soon as decisions have been made by the organizers.

We are eager to have as many young people as possible attend since they are likely to benefit most from this meeting. We have applied for funds from government and industry to partially support graduate students and postdocs. Please apply in writing via email to Maureen Morrow and state your financial needs; preference will be given to those who submit abstracts.

Social MediaThe designated hashtag for this meeting is #cshlstemcell. Note that you must obtain permission from an individual presenter before live-tweeting or discussing his/her talk, poster, or research results on social media. Click the Policies tab above to see our full Confidentiality & Reporting Policy.

We look forward to seeing you at Cold Spring Harbor in September.

Pricing:Academic Package $1,455Graduate/PhD Student Package $1,210Corporate Package $1,865Academic/Student No-Housing Package $985Corporate No-Housing Package $1,250

Regular packages are all-inclusive and cover registration, food, housing, parking, a wine-and-cheese reception, and lobster banquet. No-Housing packages include all costs except housing. Full payment is due four weeks prior to the meeting.

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Meetings

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Can Testosterone Help You Lose Weight? | Men’s Fitness

Posted: October 6, 2017 at 6:48 pm

Testosterone could be the magic weight-loss drug that men are looking for. Then again, it might not. A new study shows that obese men receiving testosterone shots lost weight, but doctors are divided on the value of the results.

Over the course of five years, obese men on hormone replacement therapy lost an average of 35 pounds each. Their body mass index also dropped from 34 to 29, moving them from the obese to overweight category. This coincided with improved cholesterol and triglyceride levels, as well as lower blood pressure.

The results are impressive, but some doctors doubt that its time to start ordering testosterone shots for obese men. The preliminary study, presented at the European Congress on Obesity, has yet to appear in a peer-reviewed journal, and was also sponsored by Bayer, which makes testosterone supplements.

Testosterone levels start to drop in most men between the ages of 40 and 50, with some menlike the ones in this studycomplaining of symptoms like erectile deficiency, fatigue and lack of energy. Testosterone replacement therapy is sometimes prescribed for these conditions. Low testosterone has also been linked to obesity.

In this study, men were prescribed testosterone shots because of their low hormone levels. Researchers also noticed that they lost weight during the study, although its unclear whether this is a direct result of the hormone therapy. Normalizing the mens testosterone levels could have increased their energy levels, which may have led to increased physical activity and weight loss.

The good news is that, in this study, testosterone therapy wasnt linked to an increased risk of prostate cancer.

It is too soon, however, to say that the hormone is a miracle weight-loss drug. Larger, more rigorous studies are needed.

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Advanced Integrative Medicine | A Contemporary Blending of …

Posted: October 5, 2017 at 12:46 pm

A Contemporary Blending of Traditional Medicine & Complementary Therapies

Career Opportunites at Advanced Integrative Medicine:

Lisa Durham won for having the most positive reviews posted on AIM. Congratulations, Lisa!

28-day Guided Summer Detoxification & Nutrition Course - Led by Dr. Diana Milling, ND

Career Opportunites at Advanced Integrative Medicine:

Advanced Integrative Medicine is excited to announce:

Advanced Integrative Medicine is looking to grow!

We are very excited at how well we have been received in our community and we are now looking to expand! We are now interviewing for Internists, Physicians Assistants and Osteopaths wanting to be involved in a leading medical office that offers alternative options to our patients. This is an excellent opportunity for someone who wants an unlimited possibility for income. Please call the office at (303) 708-0246 or email us your resume at info@aim4yourhealth.com if you are interested. We are also OPEN to New patients!

Advanced Integrative Medicines primary goal is to provide our patients with team based health services that combine Western (Allopathic) medicine with complementary treatments in a modern setting emphasizing integrated treatment modalities.

We believe that your active involvement with our providers who are Board Certified in Internal Medicine and Family Practice along with two highly trained Physician Assistants are essential to your personal health and wellness.

In addition, our professionally licensed health care providers in Clinical Psychology, Diet and Nutrition, Chiropractic, and Acupuncture services work closely together with our traditional medical providers

Mon - Fri : 8am - 5pm

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Stem Cells Can Be Collected Without Destroying Embryos …

Posted: October 5, 2017 at 12:45 pm

But obtaining human embryonic stem cells has been controversial, because until now it required the destruction of living embryos.

In the current technology, embryonic stem cells are derived by extracting a mass of cells from an embryo.

Since an early embryo is made of only a few cellsabout eight to tentaking enough to create viable cultures kills the embryo.

"Many people, including [U.S.] President Bush, are concerned about destroying life in order to save life," Lanza said.

U.S. law currently prohibits the use of federal funds for research in which a human embryo is destroyed.

Colony of Stem Cells

Last year Lanza's team showed that it's possible to remove a single cell from a mouse embryo without destroying the embryo.

Through various manipulations, the team grew that cell into a colony of mouse embryonic stem cells.

The extraction procedure is similar to that used during in vitro fertilization to remove a single cell for preimplantation genetic diagnosis (PGD).

PGD is a very early form of diagnosis that tests a human embryo for genetic abnormalities before it is implanted in a woman's uterus.

"This is a relatively simple biopsy procedure that has been used to generate over 2,000 healthy babies," Lanza said.

(See 3-D illustrations of a fetus growing in the womb.)

Using spare human embryos from in vitro fertilization for their most recent study, the scientists used a tiny pipette to extract one cell from each embryo and then grew each cell in a hormone-laden culture.

Just like in the case of PGD tests, embryos with only one cell removed would have survived and gone on to grow into fetuses. To get the most from their samples, however, Lanza's team took several cells from each embryo, destroying the embryos in the process.

From a total of 91 cells taken from 16 embryos, Lanza said his team "obtained two stable human embryonic stem cell lines, which have been growing over eight months at this point."

He says the new stem cell lines behave exactly like conventional embryonic stem cells.

"The resulting cells could be used for genetic testing as well as to create stem cells without affecting the subsequent chances of [the embryos developing into children]," Lanza said.

Ethical Quandary Resolved?

Ronald M. Green, director of the Ethics Institute at Dartmouth College in Hanover, New Hampshire, says the research directly addresses the ethical concerns that many people have about stem cell research.

"It is very, very unusual for scientific research to resolve an ethical quandary, and this is one of those rare instances," Green said. "I do believe it solves the ethical problems."

(Explore the stem cell debate in National Geographic magazine: see photos, take a poll, and join the forum.)

Scientists hope the results will soon lead to the release of U.S. federal funding for embryonic stem cell research.

"This could conform to both the ethical and maybe even the legal thinking that has motivated the [U.S.] President to oppose this," Green said.

"I hope he sees this as an opportunity consistent with his values."

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Erectile Dysfunction and Testosterone Replacement Therapy

Posted: October 4, 2017 at 2:46 am

Testosterone is a hormone produced by the testicles and is responsible for the proper development of male sexual characteristics. Testosterone is also important for maintaining muscle bulk, adequate levels of red blood cells, bone growth, a sense of well-being, and sexual function.

Inadequate production of testosterone is not a common cause of erectile dysfunction; however, when ED does occur due to decreased testosterone production, testosterone replacement therapy may improve the problem.

As a man ages, the amount of testosterone in his body naturally gradually declines. This decline starts after age 30 and continues throughout life. Some causes of low testosterone levels are due to:

Without adequate testosterone, a man may lose his sex drive, experience erectile dysfunction, feel depressed, have a decreased sense of well-being, and have difficulty concentrating.

Low testosterone can cause the following physical changes:

The only accurate way to detect the condition is to have your doctor measure the amount of testosterone in your blood. Because testosterone levels fluctuate throughout the day, several measurements will need to be taken to detect a deficiency. Doctors prefer, if possible, to test levels early in the morning, when testosterone levels are highest.

Note: Testosterone should only be used by men who have clinical signs and symptoms AND medically documented low testosterone levels.

Testosterone deficiency can be treated by:

Each of these options provides adequate levels of hormone replacement; however, they all have different advantages and disadvantages. Talk to your doctor to see which approach is right for you.

Men who have prostate cancer or breast cancer should not take testosterone replacement therapy. Nor should men who have severe urinary tract problems, untreated severe sleep apnea or uncontrolled heart failure. All men considering testosterone replacement therapy should undergo a thorough prostate cancer screening -- a rectal exam and PSA test -- prior to starting this therapy.

In general, testosterone replacement therapy is safe. It is associated with some side effects, including:

Laboratory abnormalities that can occur with hormone replacement include:

If you are taking hormone replacement therapy, regular follow-up appointments with your doctor are important.

Like any other medication, directions for administering testosterone should be followed exactly as your doctor orders. If you are unsure or have any questions about testosterone replacement therapy, ask your doctor.

SOURCE:

Get-Back-On-Track.com.

The Hormone Foundation.

News release, FDA.

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Testim VS Androgel – Testosterone Replacement Therapy

Posted: October 4, 2017 at 2:46 am

The two major testosterone gel brands are Testim and Androgel. They are very similar and generally prescribed interchangeably, but sometimes insurance wont cover one or the other. Often, I hear that they wont cover Testim and people want to know if Androgel is just as good. So here is a general guide to choosing if you are lucky enough to have the choice which one is right for you.

Testim Vs AndrogelI would try whichever your insurance covers first. If your insurance covers both medications, try whichever one has coupons or kickbacks. Ive heard people say they didnt pay any/much for Testim for the first year because the company (Auxilium) that markets the drug has a financial assistance program available for the first year.

Now that price and availability are out of the way, lets deal with smell: Testim smells. Some people think it smells good, and some cant stand it. Personally, I like it and my wife likes it. Ive found that women ask me what cologne Im wearing, and mention that they like it too. Still, if you or your wife dont like the smell of something you have to put on every day, that would be a deal-breaker. So try out a tube and see what you and, if applicable, your partner thinks about the Testim scent. Androgel doesnt have much of a smell at all.

Testim is sticky. Androgel goes on much like that hand-sanitizer stuff, while Testim seems to remain stickier longer. Some say this is why Testim seems to work better for them: Because it stays on the skin and soaks in better. These personal statements of efficacy cant be relied on as empirical data, however. But the fact that you can feel it on your skin longer, does bring up a question about Testim gel Vs Androgel: Does it take longer to soak in and, if so, does that increase the exposure time I have to worry about when it comes to my wife and children? The short answer is: NO. In-fact, according to US National Library of Medicines website, the wait-time for AndrogGel is much longer:

You should not shower, bathe, swim, or wash the place where you applied the medication for at least 2 hours after you apply Testim gel or at least 5-6 hours after you apply AndroGel .

WasteTestim comes in little single-use tubes so you go through more of them and it generates more waste. If you are eco-minded this may factor into your decision. Androgel comes in a dispenser with a little pump on it (like soap) so there is less waste.

But the real question when considering AndroGel Vs Testim is: Which works better? Which is the best? Which testosterone topical gel is going to get my testosterone levels on track fast, keep my levels steady, and keep me there for the long term since Ill be taking this stuff for many years to come? As you might guess, both brands have their fans. Personally, I like Testim. And here is a study to back up my personal preference:

Efficacy of changing testosterone gel preparations (Androgel or Testim) among suboptimally responsive hypogonadal men.Grober ED, Khera M, Soni SD, Espinoza MG, Lipshultz LI.Division of Urology, Mount Sinai Hospital and Womens College Hospital, University of Toronto, Toronto, ON, Canada.Summary of the study:

A change in testosterone gel preparation among initially unresponsive hypogonadal men is justified prior to abandoning or considering more invasive TRT. Changing from Androgel to Testim offers hypogonadal men the potential for improved clinical and biochemical responsiveness. Changing from Testim to Androgel is indicated to eliminate or minimize unwanted side effects.

Note: This study was done to find out if switching brands would help men who were unresponsive to one brand or the other.

More important to me than such a study is to find out from others who have been on TRT for more than a year, preferably several years or more, and hear about their experiences with both or either drug. Please comment below with your own experiences.

I am inclined toward a weekly injection over a daily application, but what does ones rear-end feel like after being used as a pin-cushion for decades? I dunno any bodybuilders out there want to elaborate on that?

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Cell Therapy :: Sangamo Therapeutics, Inc. (SGMO)

Posted: October 2, 2017 at 7:59 pm

Sangamo has significant experience in process development and manufacturing of modified cell therapy products gained through its T-cell and hematopoietic stem cell (HSC) programs in HIV, which were the first genome editing products to enter human clinical trials. In collaboration with Bioverativ we are also developing modified HSC treatments for beta-thalassemia and sickle cell disease. Cells are removed from the body and undergo ZFN-mediated genome editing. In these autologous therapies, the modified cells are grown and tested before being infused back into the patient.

Modified T-cells have demonstrated spectacular success in treating some cancers. With the exception of two cases these have been autologous therapies. A more useful product would be an off-the-shelf or allogeneic product that could be administered to any patient on diagnosis rather than after precious weeks of manufacturing their own cells. Using our ZFN-mediated genome editing technology to knock out genes that identify these cells as foreign to a patient, we are working to make this possibility a reality.

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For Authors – Molecular Medicine

Posted: October 1, 2017 at 10:55 pm

Following is an outline describing the instructions for submission toMolecular Medicine. Submission types include: Research Article, Review Article, Commentary, and Letter to the Editor. Submitted manuscripts should conform to the requirements set forth in the Instructions for Authors here. Incomplete or non-conforming work will be sent back to the author to be corrected and may cause delays in the review process.

CriteriaMolecular Medicineis an open access journal that seeks to publish recent original findings that elucidate the pathogenesis of disease at the molecular or physiological level, which may lead to the design of specific tools for disease diagnosis, treatment, or prevention. Manuscripts containing original material relevant to the genetic, molecular, or cellular basis of key physiologic or disease processes are considered for publication if neither the article nor any part of its essential substance, tables, or figures has been or will be published or submitted elsewhere before appearing inMolecular Medicine. Manuscripts published inMolecular Medicineshould contain human or animalin vivoorex vivodata and describe the implications of the results for human disease and medicine, at a level approachable by our broad audience.

Pre-submission EnquiryIf authors are unsure as to whether or not their manuscript comes within the scope ofMolecular Medicine, they may request advice prior to full submission. An abstract or a summary highlighting the originality and significance of the study should be submitted to the Editorial Office via the online submission system:http://mc.manuscriptcentral.com/molmed. When asked for Manuscript type, be sure to select Pre-submission Enquiry.Pre-submission inquiries sent by email will not be considered.

The pre-submission enquiry service is a courtesy and is not required prior to full submission. Pre-submission enquiries can be difficult to assess reliably andMolecular MedicineEditors cannot make an absolute commitment to have a contribution refereed before seeing the entire paper. Entire papers should not be sent as pre-submission enquiries.

Submission TypesMolecular Medicineaccepts contributions in the following formats: Research Article, Review Article, Commentary, and Letter to the Editor.

Research Article reports comprehensive data from original experimental research. This type of paper demonstrates original concepts relating to the molecular or physiological basis of human disease. Because critical evaluation and replication of findings are essential to the scientific process, these types of articles include detailed descriptions of all processes and experimental techniques utilized in the study. In some cases, the Editors may commission Research Articles. Word count is approximately 7000 (including abstract [250 words], figures [count as 250 words each, 5-6 figures are typical], and references). The specific format includes the following sections in this order: Title, Running Head, Author Names, Keywords, Abstract, Introduction, Materials and Methods, Results, Discussion, Acknowledgements, Disclosure, Footnotes, References, Tables, Figure Legends, Figures, and Supplementary Data (if applicable).

Review Article brings together and analyzes available information in a specific field. These submissions include a summary of the topic/field, a description of gaps in knowledge of the topic/field, and synthesis of information to form a testable hypothesis. Reviews discuss recent developments in the topic/field and make projections about the future direction of a particular field. In some cases, the Editors may commission Review Articles. Word count is approximately 7000 (including abstract [250 words], figures [250 words each], and references).

Commentary commissioned by the Editors. However, in some cases the Editors may consider unsolicited works. Commentaries are professional opinion pieces covering cutting-edge research topics related to disease pathogenesis and the future of medicine. These may also address an issue of concern regarding work published outside ofMolecular Medicine. In this case the commentary may be sent to the original authors for a response. While this submission type does not require data, figures, or original research, they may be included to aid in the education of the interdisciplinary audience. Word count is approximately 1500-3000 (including abstract [250 words], figures [250 words each], and references).

Letter to the Editor addresses an issue of concern regarding work published by Molecular Medicineand may include data that enhances the dialogue surrounding the work. This may be viewed as an open post-publication review of a manuscript. Once received, comments will be reviewed by the Editors and may be sent to the original authors for a response. In some cases an independent reviewer may be asked to assess the comments. Word count is approximately 800 with up to 15 references and 2 figures.

Cover LetterA cover letter should accompany each submission. The cover letter should:

To view a cover letter template, please see the freely available article: L Chipperfield, L Citrome, J Clark,et al.(2010) Authors' Submission Toolkit: A practical guide to getting your research published. Current Medical Research & Opinion. 26:8 p1968-1982.www.cmrojournal.com

Manuscripts should be submitted toMolecular Medicinevia our online submission system:http://mc.manuscriptcentral.com/molmed

Style ManualThe entire manuscript should be double-spaced and written in English with the format following the Council of Science Editors reference manual:Scientific Style and Format: The CSE Manual for Authors, Editors, and Publishers, Eighth Edition.Abbreviations may be used for genes, proteins, and other specialized names if spelled out in entirety at the first use. Any additional known names should also be included in the first use. Gene names must be italicized throughout the text.

File TypesThe following file types are NOT supported during submission: shs; exe; com; vbs; zip and docx. The maximum total size of files (in K) an author can submit is 60000. Five files may be uploaded at once. If you have difficulty submitting your file due to size restrictions please contact editor@molmed.org for assistance.

Non-Native English AuthorsThe European Association of Science Editors (EASE) has published multilingual guidelines for non-native English authors and translators. These guidelines are aimed at making scientific communication more efficient worldwide and preventing scientific misconduct. To view the multilingual guidelines please see this website:http://www.ease.org.uk/guidelines/index.shtml.

Format: Research ArticleThis specific format includes the following sections in this order: Title, Running Head, Author Names, Keywords, Abstract, Introduction, Materials and Methods, Results, Discussion, Acknowledgements, Disclosure, Footnotes, References, Tables, Figure Legends, Figures, and Supplementary Data (if applicable).

Title a title page must appear as the first page of the manuscript. The title page should include a title, running head, author list, keywords, and contact author information. The title of the paper should be 20 words or less. The title should not include acronyms or abbreviations.

Running Head this short version of the title should include a maximum of 45 letter spaces.

Author Names the author(s) list must include: the first name(s); the last/family name(s); the name of the department(s) and institution(s) in which the work was done; the institutional affiliation of each author; and the name, address, telephone number, fax number, and email address of the author responsible for correspondence. Any change in author list (additions/deletions) after paper acceptance must be justified in writing to the Editors. During online submission the full names and email addresses of all the authors are required. If the work is accepted, all authors are required to sign the Open Access Authorization andAcknowledgement of Authorship form. Molecular Medicine follows the authorship criteria put forth by the International Committee of Medical Journal Editors (ICMJE), which can be found here:http://www.icmje.org/recommendations/browse/roles-and-responsibilities/defining-the-role-of-authors-and-contributors.html#two.

Keywords five MeSH-Medline keywords not included in the title must be included. For assistance visit:http://www.nlm.nih.gov/mesh/

Abstract (250 words) should include the rationale, objectives, results, and conclusions of the study. The Abstract should read as a single, continuous piece and not be written as a structured abstract (broken into separate sections).

Introduction should discuss appropriate, relevant sources that provide context for the study and help explain how the idea for the study came to be and why it is important. The objective and hypothesis of the study at hand should be explicitly stated in this section. The Introduction section should not include any mention of observed results.

Materials and Methods this section should include sufficient detail to allow another researcher to repeat the experiment. Descriptions may be 'in brief', followed by reference to a previous report using the same procedure, or by detailed description. One sentence referring a reader to a prior publication is insufficient.

General studies should include unambiguous identification of nonbiological materials used (chemicals) including the source of such materials, the types of apparatus used, including model number and manufacturer for specialized equipment, the experimental procedure, including potential hazards, if applicable; and the types of test performed, including statistical tests.

Biological studies should include unambiguous identification of genus, species, and strain; the source of any organisms (cell line, animal stock); and age, sex, weight, and condition of organisms as appropriate.

Protein molecular weights of DNA marker sizes should be indicated on figure panels showing gel electrophoresis. The quality of RNA should be proofed according to MIQE guidelines published in 2009 by S.A. Bustinet al. in Clinical Chemistry. Nucleic acid and protein sequences should be deposited in appropriate databanks in time for the accession numbers to be included in the paper. Please see theNCBI databases Web sitefor more information.

Microscopy should include the make and model of the microscope. Type, magnification, numerical aperture of the objective lenses and acquisition software are also needed. All micrographs must include an unlabelled scale bar in the image with a description included in the figure legend.

Research on animals should include a statement that the protocol was approved by the appropriate institutional committee and complied with theGuide for the Care and Use of Laboratory Animals.This statement is required for entry into peer-review.Descriptions should include information regarding:

the animal:n, age, sex, weight, and life stage, source (supplier), genetic nomenclature, microbial/pathogen status, and information related to preparation and assignment to treatment groups (including control groups);

the environment:micro and macroenvironments, diet, water, housing;

the method:include aspects of animal care that can affect research outcomes, experimental effects, administration of substances, use of infectious agents, sample acquisition, and euthanasia.

For details seeGuidance for the Description of Animal Research in Scientific Publications.Additional resources:ARRIVE Guidelines- Animal Research: Reporting In Vivo Studies,www.nc3rs.org.uk/ArriveEQUATOR Network Promoting transparent and accurate reporting of research studies,www.equator-network.orgAAALACwebsite -http://www.aaalac.org/International regulationson animal welfare are available at:http://www.aaalac.org/resources/internationalregs.cfm

Please properly site the use of any guides in the references and number the references accordingly. For example:

Committee for the Update of theGuide for the Care and Use of Laboratory Animals, Institute for Laboratory Animal Research, Division on Earth and Life Studies. (2011) Guide for the Care and Use of Laboratory Animals. 8th edition. Washington (DC): National Academies Press. [cited 20XX Month Day]. Available from: http://oacu.od.nih.gov/regs/

Institute of Laboratory Animal Resources; Commission on Life Sciences; National Research Council. (1996)Guide for the Care and Use of Laboratory Animals. Washington (DC): National Academy Press. [cited 20XX Month Day]. Available from: http://www.nap.edu/openbook.php?record_id=5140

Clinical studies should include pertinent details about human subjects, including methods of recruitment and relevant physical characteristics. Reports of human studies must include a statement that the protocol was approved by the appropriate institutional committee or that it complied with the HelsinkiDeclaration as revised in 1983 -http://www.wma.net/en/30publications/10policies/b3/index.html. Informed consent should be obtained for all subjects. When preparing reports of randomized clinical trials, authors should refer to the checklist published in the CONSORT Statement and should include a trial profile summarizing participant flow. For additional information, please see the NIH resource: Responsible Conduct of Research -http://bioethics.od.nih.gov/These statement arerequired for entry into peer-review.

Mathematicspapers with mathematicsshould follow the guidelines suggested in the resources below:International Organization for Standardization: Quantities and Units - Part 2: Mathematical Signs andSymbols to be used in the Natural Sciences and TechnologyAmerican Mathematical Society: A Manual for Authors of Mathematical PapersHow to Report Statistics in Medicine: Annotated Guidelines for Authors, Editors and Reviewers

Statistics papers with statistical testing should state the hypothesis being tested/comparisons of interest, the name of the test, the n for each analysis, a justification for the use of that test, the alpha level for all tests, whether the tests were one- or two-tailed, and the actual P value for each test. Confidence intervals should be computed to complement the results of hypothesis tests. Discrepancies in any sample sizes due to exclusions, dropouts or missing data should be noted and explained. Data sets should be summarized with descriptive statistics, which should include the n for each data set, a clearly labeled measure of location (such as the mean or the median), and a clearly labeled measure of variability (such as the standard deviation, range, or interquartile range). Graphs should include clearly labeled error bars. Authors must state whether a number that follows the sign is a standard error of the mean (s.e.m.) or a standard deviation (s.d.).

Results original results should be presented clearly with appropriate subheadings. This section should not discuss implications or applications of the results.

Discussion should be an analytical examination of the study and results rather than a repetition of the information in the results section. It is relevant to compare the results of the study to the findings of similar studies and also to discuss the application of these results to the understanding of disease and the development of tools for disease diagnosis, treatment and prevention. The main findings should be placed in context to highlight the advance and describe how it moves the field forward. Avoid unqualified statements not supported by data.

Conclusion condenses work presented in the discussion and states the significance of the findings. Includes a statement of how the work may alter disease diagnosis, treatment, or prevention in the future.

Acknowledgments sources of financial support should be included along with any acknowledgements relevant to scientific advice or assistance.

Disclosure authors should include any necessary conflicts of interest. If none exist, the following text should be included: "The authors declare they have no competing interests as defined byMolecular Medicine, or other interests that might be perceived to influence the results and discussion reported in this paper."

Footnotes should be restricted to the title page (affiliations, corresponding author) and within tables. Footnotes on the title page are assigned consecutive superscript numbers (i.e., 1, 2, 3, etc.). Footnotes in tables are assigned consecutive, superscript capital letters (i.e., A, B, C, etc.).

References should be numbered consecutively as they are cited in the text and listed in parentheses. References first cited in tables or figure legends must be numbered so that they will be in sequence with references in the text. References should include full titles of the papers with inclusive page numbers. All authors should be listed when there are five or fewer; when there are six or more, the first author should be listed followed by "et al.'' Abbreviate the names of journals according to PubMed. Spell out names of unlisted journals. If essential, 'personal communication' may be incorporated in the appropriate place in the text. References to personal communications must be accompanied by a permission letter from the communicator authorizing publication of the comment. Manuscripts listed as in press should be numbered anda copy of the text should be submitted along with the manuscript under consideration. References to unpublished data or personal observation will not be accepted.Examples of reference styles can be found below.

Journal articles1. Gallowitsch-Puerta M, Tracey KJ. (2005) Immunologic role of the cholinergic anti-inflammatorypathway and the nicotinic acetylcholine alpha 7 receptor.Ann N Y Acad Sci.1062:209-19.

Complete books2. Tracey, KJ. (2005)Fatal Sequence:The Killer Within. New York: Dana Press. 184 pp.

Articles in books3. Forstner JF, Forstner GG. (1994) Gastrointestinal Mucus. In:Physiology of Gastrointestinal Tract.Johnson LR (ed.) Raven Press, New York, pp. 1255-1283.

Homepages4.Molecular Medicineonline [Internet]. c1994-2011. Manhasset (NY): The Feinstein Institute ofMedical Research; [cited 11 Apr 2008]. Available from http://www.molmed.org.

Tables should be included in the manuscript. Tables should be double-spaced each on its own page, portrait orientation, upright, with brief titles. Superscript capital letters should be used in consecutive order as footnotes as described above.

Figures: Instructions for FiguresFollowing is an outline describing the instructions for submission of figures to Molecular Medicine.

Acceptable File Typesinclude EPS, JPEG, and TIFF. Required resolution is 300-600 dpi. Required color mode is cyan, magenta, yellow, black (CMYK) which works best for commercial printers.

Font Should be a non-serif type, such as Arial (if you cannot use Arial, use Helvetica). Serif fonts are not acceptable. Font should be consistent within and across figures. Font size may vary, the minimum required font size is 6 points maximum font size is 12 points, the only exception being panel labels which may be 18 point, bold, all capitals. All fonts must be legible at actual print size (see column measurements below under Sizing). Line weights (.75pt 1.00 pt [2.00 pt for lines within flowcharts]; consistent within document. Symbol font may be used for special characters and Courier may be used for sequence alignments.

Capitalization Use sentence-style capitalization within figures. Capitalize the first word of each figure axis figure key label, figure title, etc.; subsequent words should be lowercase.Graph Style -Graphs should not include hatches or other patterns. Choose colors or shades of gray with enough contrast to stand out and make clear the meaning of the graph. Graph bars should be delineated with grays that differ by at least 20% in value. All controls (sham, untreated, vehicle) should be represented with white/open bars. Outline white, grey or colored bars with black. Graph lines should be .75-1.0 line weight. Please do not submit 3-D style graphs unless necessary.

Axis Labels Figures should be cited sequentially in the text using Arabic numerals. Figures should not contain more than one panel unless logically connected. Larger X and Y axis labels should be bold Arial. Axis number should be slightly smaller, using regular Arial. Use only X and Y axis lines, when appropriate. Avoid the use of complete boxes to enclose graphs. Use tick marks for only the major axis labels; smaller tick marks should be left off. Tick marks on graphs face outward and are used only for labeled quantities. Panel labels may be 18 point, bold, all capitals. Labels along the X-axis should be horizontal (if too long should be rotated 45 counter clockwise). Labels along the Y-axis should be rotated 90 counter clockwise. Labels along the Y-axis when on the right side (when there are two y-axes) should be rotated 90 clockwise. Numbers on axes are not bold. Initial symbols on axis labels should be spelled out, for example: Percent (%).

Figure Legends and Figure Keys Figure legends should include a short title and a brief explanation with sufficient detail to interpret the data presented. Do not exceed 350 words for each legend. Abbreviations should be defined at the end of the legend. Figure legends should be saved as part of the main text, not within the figures. Symbols should be in symbol font. Scale bars should be placed on images and defined in the legend. Text should not be placed over textured or shaded areas (light colored lettering on a dark background). Figure keys must be included within the legend and not in the figure itself.

Figure Layout Avoid unnecessary spacing within your figure layout. Avoid using unnecessary boxes to enclose graphs or images.

Panel Label Each panel of a multi-part figure must be labeled with a bold, capital, 18-point letter (A, B, C). Punctuation should not be included in the figure label. Labels should be placed in the upper left corner of each element and be no more than 12 mm away from the rest of the figure when viewed at 100%. Whenever possible, do not place this letter over other text or images.

Column Sizes Our journal columns are as follows: 1-column figure (2.3 inches/5.8 centimeters/166 points); 2-column figure (4.8 inches/12.3 centimeters/349 points); 3-column figure (7.3 inches/18.7 centimeters/532 points). Your figures should print at one of these sizes and still be readable and high quality.

Supplementary Data to submit supplementary data, authors should upload it to the submission site with the rest of their files. On the dropdown list of file types, the author should choose "Supplementary." This supplementary data will not be published along with the manuscript in the print journal, but will be availableonline.

Format: Other Submission TypesWhile there are no strict headings for Review Articles, Commentaries, or Letters to the Editor, authors should familiarize themselves with these content types by reading the journal online at:www.molmed.org. Word limits for these submission types have been described above. Abstract, Acknowledgements, Disclosure, Footnotes, References, Tables, Figure Legends, and Figures should adhere to the style and requirements described under Research Article.

SubmissionManuscripts should be submitted to Molecular Medicine via our online submission system:http://mc.manuscriptcentral.com/molmed. Postal submissions will not be considered. If you do not already have an account, you will need to create one. Click on 'create account' in the upper right hand corner of the screen (or, for previousMolecular Medicineauthors or reviewers, check for an existing account). Once you have completed the profile information, click the Main Menu and icon for "Corresponding Author Center." Begin a manuscript submission, fill in the required fields and upload any necessary files. While online submission can accommodate a variety of file types, authors are urged to provide their manuscripts as original Microsoft Word documents and figures as original files (figures may also be submitted as Microsoft Powerpoint slides). Click herefor assistance with submission. Confirm your work has been successfully converted to both a PDF and an HTML file. Please confirm your images are readable in the PDF and HTML files. Unreadable figures may delay the review process. Click 'submit' to send your manuscript to the Editorial Office. Should you have difficulty with this process, please contact the Editorial Office at:editor@molmed.org.

The status of your manuscript can be viewed by logging back in to this submission system. A description of status updates are below.

Awaiting Admin Processing the manuscript is being considered for the peer-review process.Under Consideration the manuscript has been sent for peer-review.Awaiting AE Preliminary Decision peer-review reports have been received.Awaiting EDB Decision Approval the manuscript is in the queue for Editorial Board Review and decision.

For additional tips on manuscript preparation and submission, authors are encouraged to read the following free paper:

L Chipperfield, L Citrome, J Clark,et al. (2010) Authors' Submission Toolkit: A practical guide to getting your research published.Current Medical Research & Opinion.26:8 p1968-1982.www.cmrojournal.com

Scientific MisconductMolecular Medicinerecognizes the importance of ethical standards in the research community and is committed to promoting ethical practices in our publication. Below are examples of the journal's commitment.

Molecular Medicineis a member of the Council of Publication Ethics (COPE) and generally follows the Code of Conduct of Journal Editors.

Members ofMolecular Medicinebelong to the Council of Science Editors (CSE). See the following White Paper by the Council: CSE's White Paper onPromoting Integrity in Scientific Publications, 2009 Update.

Molecular Medicineis a member of CrossCheck by iThenticate. iThenticate is a text duplication screening service that verifies the originality of content submitted before publication. The iThenticate software checks submissions against millions of published research papers, documents on the web, and other relevant sources. Authors, researchers and freelancers can also use the iThenticate system to screen their work before submission by visitingresearch.ithenticate.com.

FeesUpon submission authors will be charged a manuscript processing fee of $100 USD, payable by credit card only. UPDATE: As of November 2015 based on user feedback, the submission fee will be eliminated beginning January 1, 2016. If the work is accepted, authors will be charged a flat publication fee of $1500 USD. UPDATE: As of November 2015 This fee will be increased to $1750 beginning January 1, 2016. There are no additional charges for color pages, excess pages or word count. Manuscripts will not be sent for processing until this fee has been received. To see if grant funds may be used for payment, click the following link: http://oad.simmons.edu/oadwiki/OA_journal_funds. Editors and reviewers do not have access to author payment information. Ability to pay does not inform Editor and reviewer decision-making. To request a fee waiver, please contact the Editorial Office at: editor@molemed.org.Please contactfinance@molmed.orgwith any questions.

Author Acknowledgement and DisclosureUpon acceptance, all authors are required to complete an Open Access Authorization form as well as a Conflict of Interest - Disclosure form. These must be submitted electronically. All forms from all authors must be completed and submitted prior to the release of a final typeset-author approved galley.

Contact InformationThe Feinstein Institute for Medical ResearchEditorial Offices ofMolecular Medicine350 Community DriveManhasset, NY 11030 USATelephone: (516) 562-2114Fax: (516) 562-1022Email

Updated 2.December.2015

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For Authors - Molecular Medicine

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Society of Nuclear Medicine and Molecular Imaging (SNMMI)

Posted: October 1, 2017 at 10:55 pm

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Society of Nuclear Medicine and Molecular Imaging (SNMMI)

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