Littérature scientifique sur le sujet « Adipose-derived mesenchymal stem cell »
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Articles de revues sur le sujet "Adipose-derived mesenchymal stem cell"
Zahran F, Zahran F., El-Deen IM El-Deen IM, Hamed S. Hamed S et EL-Shenawy A. EL-Shenawy A. « Characterization of Adipogenic Differentiation of Mesenchymal Stem Cell Derived from Mice Adipose Tissue ». Indian Journal of Applied Research 3, no 7 (1 octobre 2011) : 18–22. http://dx.doi.org/10.15373/2249555x/july2013/7.
Texte intégralKawata, Yumiko, Eiji Ikami, Junya Nojima, Shoichiro Kokabu, Tetsuya Yoda et Tsuyoshi Sato. « Effect of Adipose Tissue-Derived Mesenchymal Stem Cells on Irradiated Bone Marrow-Derived Mesenchymal Stem Cells ». Journal of Bone Biology and Osteoporosis 4, no 1 (15 novembre 2018) : 94–98. http://dx.doi.org/10.18314/jbo.v4i1.1230.
Texte intégralAn, JH, KB Kim, SC Kwon, HJ Kim, MO Ryu, YI Oh, JO Ahn et HY Youn. « Canine adipose tissue-derived mesenchymal stem cell therapy in a dog with renal Fanconi syndrome ». Veterinární Medicína 67, No. 4 (16 février 2022) : 206–11. http://dx.doi.org/10.17221/213/2020-vetmed.
Texte intégralGerth, David J., et Seth R. Thaller. « Adipose-Derived Mesenchymal Stem Cells ». Journal of Craniofacial Surgery 30, no 3 (mai 2019) : 636–38. http://dx.doi.org/10.1097/scs.0000000000005336.
Texte intégralBunnell, Bruce A. « Adipose Tissue-Derived Mesenchymal Stem Cells ». Cells 10, no 12 (6 décembre 2021) : 3433. http://dx.doi.org/10.3390/cells10123433.
Texte intégralFranco, GG, BW Minto, LP Coelho, PF Malard, ER Carvalho, FYK Kawamoto, BM Alcantara et LGGG Dias. « Autologous adipose-derived mesenchymal stem cells and hydroxyapatite for bone defect in rabbits ». Veterinární Medicína 67, No. 1 (29 novembre 2021) : 38–45. http://dx.doi.org/10.17221/85/2020-vetmed.
Texte intégralAlió del Barrio, Jorge L., Ana De la Mata, María P. De Miguel, Francisco Arnalich-Montiel, Teresa Nieto-Miguel, Mona El Zarif, Marta Cadenas-Martín et al. « Corneal Regeneration Using Adipose-Derived Mesenchymal Stem Cells ». Cells 11, no 16 (16 août 2022) : 2549. http://dx.doi.org/10.3390/cells11162549.
Texte intégralKo, M., TH Kim, Y. Kim, D. Kim, JO Ahn, BJ Kang, S. Choi, I. Park, JH Choi et JY Chung. « Improvement of systemic lupus erythematosus in dogs with canine adipose-derived stem cells ». Veterinární Medicína 64, No. 10 (26 octobre 2019) : 462–66. http://dx.doi.org/10.17221/46/2019-vetmed.
Texte intégralLee, Rebecca, Nicoletta Del Papa, Martin Introna, Charles F. Reese, Marina Zemskova, Michael Bonner, Gustavo Carmen-Lopez, Kristi Helke, Stanley Hoffman et Elena Tourkina. « Adipose-derived mesenchymal stromal/stem cells in systemic sclerosis : Alterations in function and beneficial effect on lung fibrosis are regulated by caveolin-1 ». Journal of Scleroderma and Related Disorders 4, no 2 (25 janvier 2019) : 127–36. http://dx.doi.org/10.1177/2397198318821510.
Texte intégralHodgkinson, Tom, Francis Wignall, Judith A. Hoyland et Stephen M. Richardson. « High BMPR2 expression leads to enhanced SMAD1/5/8 signalling and GDF6 responsiveness in human adipose-derived stem cells : implications for stem cell therapies for intervertebral disc degeneration ». Journal of Tissue Engineering 11 (janvier 2020) : 204173142091933. http://dx.doi.org/10.1177/2041731420919334.
Texte intégralThèses sur le sujet "Adipose-derived mesenchymal stem cell"
ANGHILERI, Elena. « Adipose-derived mesenchymal stem cells : neuronal differentiation potential and neuroprotective action ». Doctoral thesis, Università degli Studi di Verona, 2010. http://hdl.handle.net/11562/343866.
Texte intégralAdult mesenchymal stem cells derived from adipose tissue (ASC) offer significant practical advantages over other types of stem cells (SC) for potential clinical applications, since they can be obtained from adult adipose tissue in large amounts, can be easily cultured and expanded with a very low risk for development of malignancies. We investigated in vitro the neuronal differentiation potential of human ASC with a chemical protocol and a prolonged two-step protocol, which included sphere formation and sequential culture in brain-derived neurotrophic factor (BDNF) and retinoic acid (RA). After 30 days, about 57% ASC show morphological, immunocytochemical and electrophysiological evidence of initial neuronal differentiation. In fact, ASC display elongated shape with protrusion of two or three cellular processes, selectively express nestin and neuronal molecules (including GABA-A receptor and tyroxine hydroxilase) in the absence of glial phenotypic markers. Differentiated cells show negative membrane potential (−60 mV), delayed rectifier potassium currents and TTX-sensitive sodium currents, but they are unable to generate action potential. Considering the low efficacy and the not-fully mature neuronal differentiation, we evaluated if ASC display a neuroprotective effect. Using the H2O2-stressed neuroblastoma model in vitro, we show that ASC increase cell availability (compared to fibroblasts) and protect against apoptosis. A possible mechanism involved could be the secretion of BDNF, as reported for human BM-MSC: in this regard, we indeed find high levels of BDNF in ASCcondition medium. In addition to exert neuroprotection, soluble factors secreted by ASC promote neurite outgrowth, an additional mechanism that may favor neuroregeneration. In view of these results and their immunosuppressive action (Constantin et al, 2009), ASC may be a ready source of adult MSC to treat neurodegenerative diseases.
Brown, Alice Clare. « Generating hair follicle inductive dermal papillae cells from adipose derived mesenchymal stem cells ». Master's thesis, University of Cape Town, 2018. http://hdl.handle.net/11427/29596.
Texte intégralBanani, M. A., M. Rahmatullah, N. Farhan, Zoe Hancox, Safiyya Yousaf, Z. Arabpour, Moghaddam Z. Salehi, M. Mozafari et Farshid Sefat. « Adipose tissue-derived mesenchymal stem cells for breast tissue regeneration ». Future Medicine, 2021. http://hdl.handle.net/10454/18391.
Texte intégralWith an escalating incidence of breast cancer cases all over the world and the deleterious psychological impact that mastectomy has on patients along with several limitations of the currently applied modalities, it's plausible to seek unconventional approaches to encounter such a burgeoning issue. Breast tissue engineering may allow that chance via providing more personalized solutions which are able to regenerate, mimicking natural tissues also facing the witnessed limitations. This review is dedicated to explore the utilization of adipose tissue-derived mesenchymal stem cells for breast tissue regeneration among postmastectomy cases focusing on biomaterials and cellular aspects in terms of harvesting, isolation, differentiation and new tissue formation as well as scaffolds types, properties, material–host interaction and an in vitro breast tissue modeling.
Edbom, Katarina. « Characterization of adipose derived mesenchymal stem cells received via automated extraction ». Thesis, Örebro universitet, Institutionen för medicinska vetenskaper, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-48506.
Texte intégralMacKay, Maria-Danielle L. « Characterization of Medullary and Human Mesenchymal Stem Cell-Derived Adipocytes ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1232775772.
Texte intégralPrasad, Ankur. « The role of aortic carboxypeptidase-like protein in adipose-derived mesenchymal stem cell adipogenesis and fibrosis ». Thesis, Boston University, 2013. https://hdl.handle.net/2144/12193.
Texte intégralThe prevalence of obesity and obesity related diseases are increasing worldwide. Obesity is characterized by the pathological expansion of white adipose tissue. Previous studies on white adipose tissue of obese individuals have detected inflammation and fibrosis. These conditions may cause dysregulation of the tissue, leading to negative outcomes, including type II diabetes and metabolic syndrome. Aortic carboxypeptidase-like protein (ACLP) is a secreted extracellular matrix protein that is upregulated in fibrotic lung tissue. Importantly ACLP knockout mice are protected from experimentally induced lung fibrosis. ACLP is expressed in adipose tissue and is downregulated as stem cells undergo adipogenesis. Its overexpression increases α smooth muscle actin expression and impairs adipogenesis in preadipocyte lines; however, its role in white adipose tissue fibrosis has not been fully explored. The studies presented in this thesis aimed to investigate the hypothesis that ACLP overexpression in fibrotic white adipose tissue would promote a fibroblast to myofibroblast transition and repress adipogenesis. To determine if ACLP promotes a fibroblast to myofibroblast transition, we tested the capacity of ACLP to induce α smooth muscle actin and collagen I protein expression and increase contractility of primary stromal vascular cells. To assess the effects of ACLP on adipogenesis, we tested the ability of 10T1/2 fibroblasts and stromal vascular cells to undergo adipogenesis in collagen I gels under ACLP treatment. Results presented herein demonstrate ACLP is a potent inhibitor of adipogenesis and induces an upward trend in myofibroblast proteins and RNA expression. Significantly, these studies used murine adipose-derived cells to show the effects of ACLP, suggesting these results might be reflected in adipose tissue. These experiments support a model where ACLP potentiates adipose tissue fibrosis by inhibiting adipogenesis, resulting in fewer developing adipocytes, and stimulating myofibroblast differentiation, resulting in further collagen deposition and tissue compaction. This contribution to adipose tissue dysfunction also gives ACLP a possible role in the development of obesity related diseases, including diabetes and metabolic syndrome, identifying it as a possible target for therapeutics.
PITRONE, Maria. « ISOLATION AND CHARACTERIZATION OF VISCERAL- AND SUBCUTANEOUS ADIPOSE-DERIVED MESENCHYMAL STEM CELLS : PUTATIVE ROLE IN OBESITY AND METABOLIC SYNDROME ». Doctoral thesis, Università degli Studi di Palermo, 2014. http://hdl.handle.net/10447/91235.
Texte intégralWong, Andrew P. « REGENERATIVE POTENTIAL OF MESENCHYMAL STEM CELL DERIVED EXOSOMES ». VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/5856.
Texte intégralLin, Wenyu. « Investigating the immunomodulatory properties of human embryonic stem cell-derived mesenchymal stem cells ». Thesis, Imperial College London, 2010. http://hdl.handle.net/10044/1/7060.
Texte intégralAL, HAJ GHINA. « EFFECTS OF LIPID MIXTURE AND A SELECTIVE PPARG MODULATOR ON THE DIFFERENTIATION CAPABILITIES OF HUMAN DERIVED MESENCHYMAL STEM CELLS(HADSCS) DERIVED FROM HEALTHY AN D BREAST CANCER PATIENTS ». Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/784157.
Texte intégralMetabolic syndrome is associated with many complications especially leading to life threatening disorders such as obesity and cancer. To be able to identify solutions and natural treatments, we need to investigate the underlying causes of this syndrome. Nutrition is one important factor to consider in the prevention and treatment of the metabolic syndrome. Nutrition effects almost all metabolism mechanisms in the human body. One provident effect of nutrition is adiposity. Over the recent years, an interest was noted to studying adipogenesis in relation to obesity. Different factors affect adipogenesis including natural dietary compounds to help decrease adiposity, therefore the risk of developing obesity and later on obesity related diseases such as breast cancer. To be able to study this correlation in-vitro, a wide choice of cell models can be used. Human adipose derived mesenchymal cells (hADSCs) are one of the top choices used to study adipogenesis overcoming the limitations that other cell models have in their applicability to humans regarding the prevailing difference in their metabolism and physiology. In this study, the aim was to study adipogenesis using hADSCs in presence of dietary compounds such as lipids and GMG-43AC, a natural selective peroxisome proliferator-activated receptor g (PPAR g) modulator, that seems to have a positive effect on inhibiting adipogenesis in murine 3T3-L1 cells. We wanted to investigate further on its application on human cell models and try to understand its mechanism in inhibiting this phenomenon. The protocols were set up using the THP-1 cell line, which we noticed upon using a Lipid mixture cocktail (Composition: Non-animal fatty acids; 2 μg/ml arachidonic; 10 μg/ml linoleic acid; 10 μg/ml linolenic acid: 10 μg/ml myristic acid; 10 μg/ml oleic acid; 10 μg/ml palmitic acid; 10 μg/ml stearic acid; 0.22 mg/ml cholesterol from New Zealand sheep′s wool; 2.2 mg/ml Tween-80; 70 μg/ml tocopherol acetate), a decrease in pro-inflammatory cytokines IL-6 and IL-1b. We also noticed a doseIV dependent increase of FABP-4. Our findings regarding hADSCs, that PPARγ expression and lipid accumulation was restored upon the presence of lipid mixture in breast cancer hADSCs that were derived from breast tissue. Secondly, GMG-43AC in both concentrations (0.5mM and 2mM) inhibited lipid accumulation and showed a significant decrease in the expression of adipocyte-specific genes, such as PPARγ and FABP-4 even after the full differentiation of hADSCs that were derived from lipoaspirates. This suggests that dietary compounds are important factors in adipose differentiation and diet has a big influence in the progression and prevention in many metabolic diseases, such as obesity and cancer.
Livres sur le sujet "Adipose-derived mesenchymal stem cell"
Adipose-derived stem cells : Methods and protocols. New York, NY : Humana Press, 2011.
Trouver le texte intégralMesenchymal Stem Cell Derived Exosomes. Elsevier, 2015. http://dx.doi.org/10.1016/c2013-0-15342-1.
Texte intégralTang, Yaoliang, et Buddhadeb Dawn. Mesenchymal Stem Cell Derived Exosomes : The Potential for Translational Nanomedicine. Elsevier Science & Technology Books, 2015.
Trouver le texte intégralTang, Yaoliang, et Buddhadeb Dawn. Mesenchymal Stem Cell Derived Exosomes : The Potential for Translational Nanomedicine. Elsevier Science & Technology Books, 2015.
Trouver le texte intégralAl-Anazi, KA, WK Al-Anazi et AM Al-Jasser. Update on COVID-19 Infections and the Promising Role of Mesenchymal Stem Cell Therapies in their Management. Heighten Science Publications Inc., 2020. http://dx.doi.org/10.29328/ebook1002.
Texte intégralBahadori, Mohammad Hadi. Cryopreservation of Rat Bone Marrow Derived Mesenchymal Stem Cells by Two Conventional and Open-Pulled Straw Vitrification Methods. INTECH Open Access Publisher, 2012.
Trouver le texte intégralLiu, Hong Bin. Bone Marrow Derived Mesenchymal Stem Cells Are Recruited into Injured Pancreas and Contribute to Amelioration of the Chronic Pancreatitis in Rats. INTECH Open Access Publisher, 2012.
Trouver le texte intégralChapitres de livres sur le sujet "Adipose-derived mesenchymal stem cell"
Fraser, John K., Min Zhu, Isabella Wulur et Zeni Alfonso. « Adipose-Derived Stem Cells ». Dans Mesenchymal Stem Cells, 59–67. Totowa, NJ : Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_4.
Texte intégralWeiss, Jeffrey N. « Adipose-Derived Mesenchymal Stem Cells in Osteoarthritis ». Dans Orthopedic Stem Cell Surgery, 41–48. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-73299-8_10.
Texte intégralWeiss, Jeffrey N. « Adipose-derived Mesenchymal Stem Cells in Osteoarthritis ». Dans Orthopedic Stem Cell Surgery, 107–13. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-73299-8_19.
Texte intégralVidal, Martin A., et Mandi J. Lopez. « Adipogenic Differentiation of Adult Equine Mesenchymal Stromal Cells ». Dans Adipose-Derived Stem Cells, 61–75. Totowa, NJ : Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61737-960-4_6.
Texte intégralAssoni, Amanda Faria, Giuliana Castello Coatti, Juliana Plat Aguiar Gomes, Mayra Vitor Pelatti et Mayana Zatz. « Adipose-Derived Mesenchymal Stromal Cells ». Dans Working with Stem Cells, 37–55. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30582-0_3.
Texte intégralKroeze, Robert Jan, Marlene Knippenberg et Marco N. Helder. « Osteogenic Differentiation Strategies for Adipose-Derived Mesenchymal Stem Cells ». Dans Adipose-Derived Stem Cells, 233–48. Totowa, NJ : Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61737-960-4_17.
Texte intégralKim, Yeon Jeong, et Jin Sup Jung. « Methods for Analyzing MicroRNA Expression and Function During Osteogenic Differentiation of Human Adipose Tissue-Derived Mesenchymal Stem Cells ». Dans Adipose-Derived Stem Cells, 401–18. Totowa, NJ : Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61737-960-4_29.
Texte intégralZachar, Vladimir, Jeppe Grøndahl Rasmussen et Trine Fink. « Isolation and Growth of Adipose Tissue-Derived Stem Cells ». Dans Mesenchymal Stem Cell Assays and Applications, 37–49. Totowa, NJ : Humana Press, 2011. http://dx.doi.org/10.1007/978-1-60761-999-4_4.
Texte intégralDubois, Severine G., Elizabeth Z. Floyd, Sanjin Zvonic, Gail Kilroy, Xiying Wu, Stacy Carling, Yuan Di C. Halvorsen, Eric Ravussin et Jeffrey M. Gimble. « Isolation of Human Adipose-derived Stem Cells from Biopsies and Liposuction Specimens ». Dans Mesenchymal Stem Cells, 69–79. Totowa, NJ : Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_5.
Texte intégralWeiss, Jeffrey N. « Allogeneic Adipose Tissue-Derived Mesenchymal Stem Cells (GXCPC1) for Knee Osteoarthritis ». Dans Orthopedic Stem Cell Surgery, 155–57. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-73299-8_28.
Texte intégralActes de conférences sur le sujet "Adipose-derived mesenchymal stem cell"
Katsube, Yoshihiro, Ousuke Hayashi, Motohiro Hirose et Hajime Ohgushi. « Adipose Tissue-derived Mesenchymal Stem Cells have Lower Osteogenic Potential than Bone Marrow-derived Mesenchymal Stem Cells ». Dans In Commemoration of the 1st Asian Biomaterials Congress. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812835758_0005.
Texte intégralGuo, Bao-Feng, Ling Zhang, Wei-Tian Yin, Kun Ji et Zhuang Wei. « Multipotential Capacity of Human Adipose-Derived Mesenchymal Stem Cells ». Dans 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5517449.
Texte intégralLevy, Debora, Suelen Silva, Thatiana Melo, Jorge Ruiz, Cesar Isaac, Maíra Fidelis, Alessandro Rodrigues et Sergio Bydlowski. « Abstract A71 : Effect of oxysterols in adipose tissue-derived mesenchymal stem cell ». Dans Abstracts : AACR International Conference held in cooperation with the Latin American Cooperative Oncology Group (LACOG) on Translational Cancer Medicine ; May 4-6, 2017 ; São Paulo, Brazil. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1557-3265.tcm17-a71.
Texte intégralRitter, A., A. Friemel, NN Kreis, SC Hoock, S. Roth, U. Kielland-Kaisen, D. Brüggmann, C. Solbach, F. Louwen et J. Yuan. « Primary cilia are dysfunctional in obese adipose-derived mesenchymal stem cells ». Dans 62. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe – DGGG'18. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1671441.
Texte intégralErdost, Hatice. « ‘Comparison of Subcutan and Inguinal Adipose Tissue Derived Mesenchymal Stem Cells’ ». Dans 15th International Congress of Histochemistry and Cytochemistry. Istanbul : LookUs Scientific, 2017. http://dx.doi.org/10.5505/2017ichc.pp-53.
Texte intégralSharaf, K., A. Kleinsasser, O. Gires, M. Canis, S. Schwenk-Zieger et F. Haubner. « Molecular characterization of lipoaspirate-derived adipose mesenchymal stem cells in wound healing ». Dans Abstract- und Posterband – 90. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Digitalisierung in der HNO-Heilkunde. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1686895.
Texte intégralKuca-Warnawin, E., U. Skalska, M. Plebanczyk, I. Janicka, U. Musialowicz, K. Bonek, P. Głuszko et E. Kontny. « P116 Basic characteristics of adipose-derived mesenchymal stem cells of ankylosing spondylitis patients ». Dans 39th European Workshop for Rheumatology Research, 28 February–2 March 2019, Lyon, France. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2018-ewrr2019.104.
Texte intégralSkalska, Urszula, Ewa Kuca-Warnawin, Tomasz Burakowski, Anna Kornatka, Iwona Janicka, Urszula Musiałowicz et Ewa Kontny. « 03.14 Comparison of immunosuppressive potential of rheumatoid adipose mesenchymal stem cells derived from articular and subcutaneous adipose tissues ». Dans 37th European Workshop for Rheumatology Research 2–4 March 2017 Athens, Greece. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2016-211049.14.
Texte intégralKuca-Warnawin, E., U. Skalska, I. Janicka, K. Bonek, P. Głuszko, W. Maslinski et E. Kontny. « P115/O19 Immunomodulatory activity of adipose-derived mesenchymal stem cells of ankylosing spondylitis patients ». Dans 39th European Workshop for Rheumatology Research, 28 February–2 March 2019, Lyon, France. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2018-ewrr2019.103.
Texte intégralAlihemmati, Zakieh, Bahman Vahidi et Nooshin Haghighipour. « Mechanical modulation study of an adipose-derived mesenchymal stem cell under pressure loading : A numerical investigation on cell engineering ». Dans 2014 21th Iranian Conference on Biomedical Engineering (ICBME). IEEE, 2014. http://dx.doi.org/10.1109/icbme.2014.7043893.
Texte intégralRapports d'organisations sur le sujet "Adipose-derived mesenchymal stem cell"
Donohue, Henry J., Christopher Niyibizi et Alayna Loiselle. Induced Pluripotent Stem Cell Derived Mesenchymal Stem Cells for Attenuating Age-Related Bone Loss. Fort Belvoir, VA : Defense Technical Information Center, septembre 2013. http://dx.doi.org/10.21236/ada606237.
Texte intégralDonahue, Henry J. Induced Pluripotent Stem Cell Derived Mesenchymal Stem Cells for Attenuating Age-Related Bone Loss. Fort Belvoir, VA : Defense Technical Information Center, juillet 2012. http://dx.doi.org/10.21236/ada581680.
Texte intégralBrennen, William N. Bone Marrow-derived Mesenchymal Stem Cells (MSCs) as a Selective Delivery Vehicle for a PSA-Activated Protoxin for Advanced Prostate Cancer. Fort Belvoir, VA : Defense Technical Information Center, mars 2013. http://dx.doi.org/10.21236/ada580995.
Texte intégralBrennen, William. Bone Marrow-derived Mesenchymal Stem Cells (MSCs) as a Selective Delivery Vehicle for a PSA-Activated Protoxin for Advanced Prostate Cancer. Fort Belvoir, VA : Defense Technical Information Center, avril 2014. http://dx.doi.org/10.21236/ada602710.
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