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Master of Science in Biotechnology | Advanced Academic …

Posted: November 5, 2015 at 2:44 am

Register for November 12 MS in Biotechnology, MS in Bioinformatics, and Certificate in Biotechnology Education Open House in Baltimore.

The Johns Hopkins MS in Biotechnology offers a comprehensive exploration of basic science, applied science, and lab science, with an industry focus. The program gives you a solid grounding in biochemistry, molecular biology, cell biology, genomics, and proteomics.

This 10-course degree program is thesis-optional, part-time, and can be completed fully online. Our curriculum will prepare you to engage in research, lead lab teams, make development and planning decisions, create and apply research modalities to large projects, and take the reins of management and marketing decisions.

Many students like the flexibility of the general degree; it allows them to tailor the coursework to meet their individual career goals. The program also offers five different concentrations: biodefense, bioinformatics, biotechnology enterprise, regulatory affairs, or drug discovery.

Onsite courses are taught during evenings or weekends at either the universitys Homewood Campus in Baltimore, MD or the Montgomery County Campus in Rockville, MD. Courses are also offered in our state-of-the-art lab.

Each year, students of the MS in Biotechnology have the opportunity to apply for a fellowship with the National Cancer Institute at NIH. This fellowship, which requires onsite research as well as onsite courses for the Molecular Targets and Drug Discovery Technologies concentration at the Montgomery Count Campus, awards students with a stipend while providing them with useful experience in the arena of cancer research. Learn more about this fellowship and apply here.

Note: We currently are not accepting applications to the online Master of Science in Biotechnology from students who reside in Kansas. Students should be aware of additional state-specific information for online programs.

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Statement on Stem Cells and Cell Therapies for Lung Diseases

Posted: November 4, 2015 at 6:46 am

DATE APPROVED: June 23, 2012

The American Lung Association strongly supports research to prevent lung disease, and reduce exacerbation of lung disease, discover cures and improve the diagnosis of lung disease. The research should include basic, translational clinical, biomedical, behavioral and environmental areas. In addition, research should investigate measures to eliminate disparities in lung disease morbidity and mortality for low socioeconomic and minority populations. Research should be conducted in a legal, ethical and humane manner.

The American Lung Association supports increased federal funding levels for biomedical, behavioral, epidemiological, environmental and intervention research and research training programs, including but not limited to those conducted by the National Institutes of Health, the Centers for Disease Control and Prevention, the Agency for Healthcare Research and Quality, the Department of Veterans Affairs and the Environmental Protection Agency.

The American Lung Association recognizes the critical role animal research has played in making medical advances. The American Lung Association strongly supports full compliance with the existing rules and regulations that assure the humane and compassionate management of laboratory animals. We encourage all forms of biomedical research involving animals that have been carefully scrutinized and deemed worthy by qualified experts, and we oppose all efforts to exclude the use of animals whenever they are essential for research.

The American Lung Association recognizes that research with human stem cells offer significant potential to further our understanding of fundamental lung biology and to develop cell-based therapies to treat lung disease. The American Lung Association supports the responsible pursuit of research involving the use of human stem cells.

The American Lung Association requires that the research it supports follow ethical standards including adherence to all applicable federal, state and local rules and regulations. All relevant Institutional Review Boards (IRB)/Human Subjects Committees should review and approve research proposals involving human subjects. Research involving animal subjects must also undergo committee Institutional Animal Care and Use Care (IACUC) review and approval as well as all other review processes as appropriate for the proposed research. Failure to adhere to such processes should result in termination of research support.

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Statement on Stem Cells and Cell Therapies for Lung Diseases

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Front Matter | Guidelines for Human Embryonic Stem Cell …

Posted: November 4, 2015 at 6:46 am

COREY S. GOODMAN (Chair),

Renovis Inc., South San Francisco, California

ANN M. ARVIN,

Stanford University School of Medicine, Stanford, California

JEFFREY L. BENNETZEN,

University of Georgia, Athens, Georgia

RUTH BERKELMAN,

Emory University, Atlanta, Georgia

R. ALTA CHARO,

University of Wisconsin, Madison, Wisconsin

DENNIS CHOI,

Merck Research Laboratories, West Point, Pennsylvania

JEFFREY L. DANGL,

University of North Carolina, Chapel Hill, North Carolina

PAUL R. EHRLICH,

Stanford University, Palo Alto, California

JAMES M. GENTILE,

Research Corporation of America, Tucson, Arizona

ED HARLOW,

Harvard Medical School, Boston, Massachusetts

DAVID HILLIS,

University of Texas, Austin, Texas

KENNETH F. KELLER,

University of Minnesota, Minneapolis, Minnesota

RANDALL MURCH,

Virginia Polytechnic Institute and State University, Alexandria, Virginia

GREGORY A. PETSKO,

Brandeis University, Waltham, Massachusetts

STUART L. PIMM,

Duke University, Durham, North Carolina

BARBARA A. SCHAAL,

Washington University, St. Louis, Missouri

JAMES TIEDJE,

Michigan State University, East Lansing, Michigan

KEITH YAMAMOTO,

University of California, San Francisco, California

FRANCES E. SHARPLES, Director

KERRY A. BRENNER, Senior Program Officer

ROBIN SCHOEN, Senior Program Officer

MARILEE K. SHELTON-DAVENPORT, Senior Program Officer

ROBERT T. YUAN, Senior Program Officer

ADAM P. FAGEN, Program Officer

ANN REID, Program Officer

EVONNE P. Y. TANG, Program Officer

SETH STRONGIN, Senior Program Assistant

MATTHEW D. MCDONOUGH, Program Assistant

DENISE GROSSHANS, Financial Associate

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Front Matter | Guidelines for Human Embryonic Stem Cell ...

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Stem and Branches | Radical Botany

Posted: November 3, 2015 at 6:49 am

As they presented the herb to me they told me to drop it on the earth and when it hit the earth it took root and flowered. You could see a ray of light coming up from the flower, reaching the heavens, and all the creatures of the universe saw the light. Black Elk (in DeMaille, The Sixth Grandfather)

Apical Meristem Cell tissue - the God force

Ok, being the total plant nerd that I am; I get very excited about teaching about parts of the plant. I mean it blows my mindthat all you have to do is cut a branch, place it in water, and watch it grow roots. How does that happen? What would happen if humans could do the same and just grow new parts? (clue: stem cells)

And, a second amazing fact about stems and branches is that you can grafta branch of one plant on to another plant and promote new and interesting growth and fruit. Pure magic! (More on grafting later).

What is happening here? It all goes back to the most magical part of a plant-the meristem cell. You know, the God-particle magical cell that stores all the DNA of the plant and allows parts of the plant to regenerate, accept cells from other plants, and grow itself from an injured part.

Let me explain in more detail. (Now dont get bored with all this plant physiology facts, in the end it all is just amazing and your knowledge of living with, growing and ingesting plants will grow exponentially!)

Meristem tissue in most plants consists of undifferentiated meristematic cells. With the apical meristem cells the tissue either heading downward and becoming roots or heading upwards and becoming stem, branch, leaves and flower are considered to be indeterminate or undifferentiated, in that they do not possess any defined end fate. The meristem cells remember that they are going to grow into a tree, a shrub, a wildflower etc, but allow a variety of changes to happen to the tissue. Where ever these cells appear in the plant, there can be new growth, including growing new parts. These types of cells seem to store the DNA of any part of the plant. The apical meristem, or growing tip, is a completely undifferentiated meristematic tissue found in the buds and growing tips of roots in plants. Its main function is to begin growth of new cells in young seedlings at the tips of roots and shoots (forming buds, among other things). Meristem cells cause the plant growth to take place in a very organized yet adaptive process. Now, meristem cells can become differentiated after they divide enough times and reach a node or internode. As the plant grows upward driven by apical meristem cells the tissue begins to organize itself into stem, branch, leaves and flower. These cells divide rapidly and are found in zones of the plant where much growth can take place. That is why you can graft one part of a plant to another part of the plant if it is in the right zone or node and if the two plants share the same type of DNA. Plants must be closely related for grafting to be successful.

For tissues to knit successfully, the cambium layers (full of fast dividing meristem cells) and rootstock must be brought into firm contact. The cambium a continuous narrow band of thin-walled, regenerative cells just below the bark or rind grows to form a bridge or union between the two parts in days. The same cells are found at the joint of a branch which allows it to grow new roots at the cut. Now, not all plants can grow roots from a branch. You need to study each plant for its particular characteristics.

SEED TO STEM THE JOURNEY BEGINS

The stem begin its journey with the seed opening up and a dicot or monocot leaf revealing itself.

A monocot (a flowering plant that produces an embryo seed with single cotyledons) will produce only one leaf. A dicot will produce two embryonic seed leaves or cotyledon. The cotyledon is a seed leaf the first to appear as the seed sprouts. It appears at the same time that root tissue appears.

Next a shoot appears (new stem) and sends out growth. The apical meristem cell structure is leading the way. We assume that the stem is heading upward toward light but a contradiction to this rule would be stems that spread downward or sideways like potatoes, tulip bulbs and other tubers. A strawberry plant will create a stolon or sideways stem to propagate new growth. A vine has a long trailing stem that grows along the ground or along anything it can attach to.

The three major internal parts of a stem are the xylem, phloem, and cambium. The xylem and phloem are the major components of a plants vascular system. A cambium is a lateral meristem that produces secondary tissues by cell division. The cambium area is located just under the epithelial (outer most area of the stem) and is very active in cell growth. It is this area that is tapped into when attempting grafting.

Stem tissue is actually organized into pipe-like vascular bundles held together by pith and cortex tissues. These tissues are used for pipelines of fluid transport, connecting leaves, stems and roots. They also serve as a supportive structure for the stem. The stem is also made up of other substances that allow it to remain flexible so that it will not break easily. Depending on what kind of plant is growing, a great tree or a wildflower, the stem may become a thick trunk with layers of vascular cambium, cork and hard bark or a more herbaceous plant. The trunk of a tree is its main stem. And, yes plants can have more than one stem. The stem that branches is called a branch.

Stems may be long, with great distances between leaves and buds (branches of trees, runners on strawberries), or compressed, with short distances between buds or leaves (fruit spurs, crowns of strawberry plants, dandelions). All stems must have buds or leaves present to be classified as stem tissue.

An area of the stem where leaves are located is called a node. Nodes are areas of great cellular activity and growth, where auxiliary buds develop into leaves or flowers. The area between nodes is called the internode. Nodes are protected when pruning back a plant. Destruction of the nodes can result in long non-fruiting branches.

MODIFIED STEMS

Although typical stems are above-ground trunks and branches, there are modified stems which can be found above and below the ground. The above-ground modified stems include crowns, stolons, and spurs and the below-ground stems are bulbs, corms, rhizomes, and tubers.

STEM FUNCTION

NATIVE PLANT PROPAGATION BY CUTTINGS.

Taking cuttings from native plants to propagate them is especially helpful in preserving what is left of many species. There is no digging or destroying plants. Forest communities are not damaged.

The process of removing a plant part then having that part grow into a genetically exact replica of the original plant is called cutting propagation. It is a plant cloning technique. The plant part that is removed is called a cutting. Plants can be propagated from root cuttings, leaf cuttings, stem cuttings, etc.

Some amazing Cascadian bioregion native plants that root from branches are: Pacific Willow (Salix lucida), Hookers Willow (Salix hookeriana), Pacific Ninebarks (Physocarpus capitatus), and Snowbush (Ceanothus velutinus). All are great attractors of important pollinators and Snowbush will fix nitrogen in the soil.

The first peoples of Cascadia built summer fishing and hunting huts along marshes and streams by placing freshly cut Willow in circles. The Willow would root and grow into a shelter and hunting blind. Today, some wonderful garden trellis have been e
rected using live Willow.

VOCABULARY

REFERENCES

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Cloning advance using stem cells from human adult reopens …

Posted: November 3, 2015 at 6:49 am

Scientists have grown stem cells from adults using cloning techniques for the first time bringing them closer to developing patient-specific lines of cells that can be used to treat a whole host of ailments, from heart disease to blindness.

The research, described in Thursdays online edition of the journal Cell Stem Cell, is a controversial advance likely to reopen the debate over the ethics of human cloning.

The scientists technique was similar to the one used in the first clone of a mammal, Dolly the sheep, which was created in 1996.

They reprogrammed an egg cell by removing its DNA and replaced it with that of an adult donor. Scientists then zapped the cell with electricity, which made it divide and multiply. The resulting cells were identical in DNA to the donor.

The first success in humans was reported last year by scientists at the Oregon Health & Science University and the Oregon National Primate Research Center. But they used donor cells from infants. In this study, the cells came from two men, a 35-year-old and a 75-year-old.

Paul Knoepfler, an associate professor at the University of California at Davis who studies stem cells, called the new research exciting, important, and technically convincing.

In theory you could use those stem cells to produce almost any kind of cell and give it back to a person as a therapy, he said.

In their paper, Young Gie Chung from the Research Institute for Stem Cell Research for CHA Health Systems in Los Angeles, Robert Lanza from Advanced Cell Technology in Marlborough, Mass., and their co-authors emphasized the promise of the technology for new therapies. What they didnt mention but was clear to those working with stem cells was that their work was also an important discovery for human cloning.

While the research published Thursday involves cells that are technically an early stage embryo, the intention is not to try to grow them into a fully formed human. However the techniques in theory could be a first step toward creating a baby with the same genetic makeup as a donor.

Bioethicists call this the dual-use dilemma.

Marcy Darnovsky, executive director of the Berkeley, Calif.-based Center for Genetics and Society, explained that many technologies developed for good can be used in ways that the inventor may not have intended and may not like.

This and every technical advance in cloning human tissue raises the possibility that somebody will use it to clone a human being, and that is a prospect everyone is against, Darnovsky said.

The research was conducted in California by a large team that included representatives from both academia and industry and was funded by a private medical foundation and South Koreas Ministry of Science.

From a technical standpoint, the technique called somatic-cell nuclear transfer is far from perfect. Chungs team attempted the cloning 39 times and only two tries produced embryos. At first they couldnt get the cells to multiply. But it turned out that if the researchers waited two hours instead of 30 minutes before trying to coax the cells, it worked.

We have reaffirmed that it is possible to generate patient-specific stem cells using [this] technology, Chung said.

Shoukhrat Mitalipov, director of the Center for Embryonic Cell and Gene Therapy at Oregon Health & Science University, developed the method that Chungs group built upon. He emphasized that the work involves eggs that have not been fertilized.

There will always be opposition to embryonic research, but the potential benefits are huge, Mitalipov said.

Seventeen years ago, news about Dollys birth led to impassioned calls for a ban on human cloning for the purpose of producing a baby who is a genetic copy of someone else. Several countries took measures to limit or outlaw such work. But in the United States, the issue became entangled in the politics of abortion, and Congress became deadlocked. Some lawmakers called for a ban on reproductive human cloning, but others refused to support such legislation unless it included a ban on human cloning whether it was for the purposes of reproduction or for the development of new therapies.

President George W. Bush brokered a compromise of sorts, restricting federal funding from stem cell research that results in harm to a human embryo.

At least 15 states have laws addressing human cloning. About half of them ban both reproductive and therapeutic cloning.

Since embryonic stem cell research began to take off 15 years ago, one of the main challenges scientists have faced is getting the material for their experiments. Many had been getting the cells from embryos left over from fertility treatments, but religious groups such as the U.S. Conference of Catholic Bishops vehemently objected to this, arguing that it involves killing a human being because the research involved fertilized eggs.

About seven years ago, scientists discovered they could use a different, molecular approach, called induced pluripotent stem cells, that could turn ordinary cells into stem cells without the need for an egg. While this technique did not present the same ethical issues, researchers soon found that some of the new cells had glitches, and there is still debate over how significant the flaws are. The research conducted by Mitalipov and Chung provides a second way of producing those cells through laboratory techniques.

Ariana Eunjung Cha is a national reporter. She has previously served as the Post's bureau chief in Shanghai and San Francisco, and as a correspondent in Baghdad.

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Home Institute for Human Genetics at UCSF

Posted: November 3, 2015 at 6:47 am

Y.W. Kans pioneering research into the hemoglobinopathies sickle cell anemia and thalassemia has widely impacted genetic research, diagnostics, and treatment of human disease. The Institute for Human Genetics is proud to recognize Y.W. Kan with a symposium honoring his decades-long contributions.

Y.W. Kan arrived at UCSF in the 1970s when he and many others (including Herb Boyer and Bishop & Varmus) helped usher in the era of molecular genetics. With long-time collaborator Andre Dozy, he discovered the first polymorphism in human DNA by Southern blot analysis in 1978, launching the ability to map genes on human chromosomes.

He and another long-time collaborator, Judy Chang, used those same techniques in 1979 to show how missing genes cause disease. He is the recipient of many national and international awards for his contributions. He continues to investigate the treatment of these diseases using stem cell and iPS cell therapies.

The Symposium will feature presentations from James Gusella, Katherine High, Dennis Lo, Bertram Lubin, Robert Nussbaum, Stuart Orkin, and Griffin Rodgers. Stuart Orkin will be featured as the 2015 Charles J. and Lois B. Epstein Visiting Professor.

Featured topics will includegene mapping, gene therapy, hemoglobinopathies, and non-invasive prenatal testing.

The IHG Symposium will be held November 2, 2015 at 1:00-6:30 in Cole Hall on the UCSF Parnassus campus and will include a poster session and awards.

IHG Symposium website|Register Now

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Keystone Symposia Stem Cells and Cancer

Posted: November 2, 2015 at 10:52 am

Registered Attendees

Registered attendees (and speakers, organizers, etc.) will have access to the following items from their Account page:

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All programs are subject to change. Check this site for updates.

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Twitter hashtag for this meeting: #KSstemcell

WARNING: Please be advised that a few meeting participants have received calls and emails from a number of different housing services "Exhibitors Housing Services", "Global Housing", etc. THESE COMPANIES ARE NOT AFFILIATED WITH KEYSTONE SYMPOSIA and are not authorized by Keystone Symposia to contact you. These companies may tell you that the meeting is filling and seek to take your lodging reservation and obtain your credit card number. We highly recommend that you not make a reservation with these companies or any other housing service! These companies' representations to participants have been misleading. Please report to Keystone Symposia any calls or correspondence you might have received and book only through the lodging link on our website, an established travel agency, or directly with the hotel.

*All deadlines end at 11:59 PM US Mountain Standard Time

Abstract Details: It is best to submit your abstract early. Abstract and registration spaces are limited and may fill prior to the abstract or discounted registration deadlines. Submitting an abstract does not constitute or guarantee registration.

Submitting your abstract early allows us to:

Details: It is best to submit your abstract early. Abstract and registration spaces are limited and may fill prior to the abstract or discounted registration deadline. Submitting an abstract does not constitute or guarantee registration.

Submitting your abstract by the Abstract Deadline allows us to:

(Discounted Abstract Deadline: is November 4, 2015)

*Includes 50.00 USD of your abstract submission fee

*Includes 50.00 USD of your abstract submission fee

Registration spaces are limited and may fill prior to discounted registration deadline.

SUNDAY, MARCH 6

18:0020:00

No registration fees are used to fund alcohol served at this function.

08:0009:00

Provide a stimulating and dynamic overview of some of the major ideas and trends shaping the field.

09:0011:15

Stability and reversibility of the stem cell state, lessons from model systems, comparisons with normal stem cells and self-renewal.

17:0019:00

Cooperativity, niche and immune interaction.

19:0020:00

No registration fees are used to fund alcohol served at this function.

08:0011:00

Control of birth, dormancy and expansion of normal and malignant stem cells/de novo human tumorigenesis.

17:0019:00

Exploration of the role of developmental pathways (eg. Notch, Wnt, Hippo, BMP, RSPO) in CSC biology.

19:0020:00

No registration fees are used to fund alcohol served at this function.

08:0011:00

EMT, plasticity, lineage tracing, clonal tracking and tumors as evolving ecosystems.

17:0019:00

New therapeutic opportunities to target CSCs.

19:0020:00

No registration fees are used to fund alcohol served at this function.

08:0010:15

Therapeutic strategies for targeting CSC in the clinic.

17:0018:45

CSC metabolism, ROS involvement-control, epigenetics and miRNA.

18:4519:00

19:0020:00

No registration fees are used to fund alcohol served at this function.

20:0023:00

Entertainment is not subsidized by conference registration fees nor any U.S. federal government grants. Funding for this expense is provided by other revenue sources.

Click here for more information on Industry Support and Recognition Opportunities.

If you are interested in becoming an advertising/marketing in-kind partner, please contact: YvonnePsaila, Director, Marketing and Communications, Email: yvonnep@keystonesymposia.org, Phone:+1 970-262-2676

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Stem Cells | Arizona Pain Specialists – Phoenix …

Posted: November 2, 2015 at 10:52 am

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The Arizona Stem Cell Center

Posted: November 2, 2015 at 10:52 am

Welcome to the webpage for The Arizona Stem Cell Center.

We are the first and original facility offering autologous stem cell transplants derived from adipose tissue in Arizona.

Our unique and innovative process allows us to extract several million stem cells from a single fat biopsy. Our extraction technique involves minimal handling of the cells and same day transplantation. Using a patient's own tissue as the source for cells minimizes rejection of the transplanted tissues, potentially maximizing the effectiveness of the transplant.

Here at Total Wellness/AZ Stem Cell Center, we have been using the technique of PRP (Platelet Rich Plasma) for the past decade for musculoskeletal injuries, autoimmune conditions like Lupus and Multiple Sclerosis, degenerative conditions like osteoarthritis, Parkinson's Syndrome and ALS (Amyotrophic Lateral Sclerosis) and chronic viral conditions (including Epstein-Barr, Cytomegalovirus and Herpes viruses). This is an incredibly versatile therapy that has its roots in the eclectic European medical armamentarium of the 1930's.

Platelet rich plasma can be employed as a matrix graft, often referred to as an autologous tissue graft. This platelet-rich plasma (PRP) matrix is defined as a "tissue graft incorporating autologous growth factors and/or autologous undifferentiated cells in a cellular matrix where design depends on the receptor site and tissue of regeneration." (Crane D, Everts PAM. Practical Pain Management. 2008; January/February: 12- 26) 2008). We enrich the autologous tissue graft with hyaluronic acid for stem cell transplants.

The hypothesized reason why PRP with hyaluronic acid is so useful in autologous tissue grafts with stem cells is that platelets, a normal blood cell that aids in clotting, contain multiple growth factors that stimulate tissue growth. In particular, PRP stimulates the growth of collagen; the main component of connective tissue such as tendons and cartilage. These growth factors include transforming growth factor-? (TGF-B), fibroblast growth factor, platelet-derived growth factor, epidermal growth factor, connective tissue growth factor, and vascular endothelial growth factor.

These growth factors normally recruit undifferentiated stem cells to the site of injury and stimulate new tissue growth. Another constituent of platelets, stromal cell derived factor I alpha allows the newly recruited cells to adhere to the area. Hyaluronic acid is a nutritionally supportive polysaccharide substrate for stem cells that is found abundantly in embryonic tissue. When stem cells are harvested from the patient's own tissues, PRP helps to activate the stem cells to actively become a desired tissue line and Hyaluronic Acid helps support.

In addition, when used with stem cells harvested from the patient's own tissue, PRP messages the stem cells to multiply quickly. This inflammatory response is a major driver of appropriate healing response.

An important consideration is that PRP needs to be prepared in a way to ensure a maximal amount of platelets along with a high concentration of growth factors. Obviously, the more growth factors that can be delivered to the site of injury, the more likely tissue healing takes place. We have found that creating a matrix of Hyaluronic acid (a base connective tissue material) with the PRP and the addition of other growth factors can tremendously expedite the healing process. We are the only clinic in the world to integrate stem cell transplantation with PRP.

Neither Statements, nor products on this site, have been evaluated nor approved by the FDA. Total Wellness offers autologous stem cell treatments. These are not approved treatments, drugs, new drugs, or investigational drugs. We do not manufacture products. If you have concern with a treatment or product that we perform or produce, and think we may be violating any USA law, please contact us immediately, so that our legal team can investigate the matter or concern. All statements, opinions, and advice provided by this website, via wire, or by educational seminars, is provided for educational information only. We do not diagnose nor treat via this website or phone. We offer the above therapies via a doctor/patient established relationship which requires direct contact with the physician. Again, visitors should be aware that we are not claiming that any applications, or potential applications using these autologous treatments, are approved by the FDA, or are even effective. We do not claim that these treatments work for any listed nor unlisted condition, intended or implied.

Call for an appointment

AZ Stem Cell Center14991 W. Bell Rd. Surprise, AZ 85374 (623) 977-0077

info@azstemcellcenter.com

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Treatments | Arizona Pain Stem Cell Institute – Scottsdale …

Posted: November 2, 2015 at 10:52 am

Treatmentsadmin2014-09-18T23:28:24+00:00

The Arizona Pain Stem Cell Institute is committed to delivering the most advanced regenerative treatments for chronic pain conditions and studying their efficacy through research studies. These treatments include:

Blood is drawn from the patient and centrifuged. The middle layer, which is rich in platelets and growth factors necessary for healing is drawn out and injected into the site of injury/degeneration. This treatment can be used to treat shoulder, hip, knee, SI, facet joints, etc. Read More

Amniotic tissues are collected from donors after planned caesarean live births. These tissues are preserved and screened to verify tissue safety. FlGraft contains pluripotent cells (capable of differentiating into different cell lines; AKA stem cells) as well as collagen matrices that serve as scaffolding on which the body can rebuild tissues.FlGraft is injected into the patient at the target area (same areas treated with PRP). Read More

Bone marrow is drawn from the patients iliac crest (hip bone). This bone marrow is then centrifuged and the stem cell rich portion is concentrated and then injected into the patient at the targeted area. This treatment will be used to treat joints (shoulder, hip, knee, SI, facet). Read More

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