Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jeffrey, Mosenson"'
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 7, Iss C, Pp 31-41 (2017)
Muscle stem cells (MuSCs) hold great therapeutic potential for muscle genetic disorders, such as Duchenne muscular dystrophy (DMD). The CRISP/Cas9-based genome editing is a promising technology for correcting genetic alterations in mutant genes. In t
Externí odkaz:
https://doaj.org/article/e8ab65205786447ca990a73143c0fed3
Autor:
Zhonghui Zhang, Yuanfan Hong, Di Xiang, Pei Zhu, Elise Wu, Wen Li, Jeffrey Mosenson, Wen-Shu Wu
Publikováno v:
Stem Cell Reports, Vol 4, Iss 4, Pp 645-657 (2015)
miR-302/367 is the most abundant miRNA cluster in human embryonic stem cells (hESCs) and can promote somatic cell reprogramming. However, its role in hESCs remains poorly understood. Here, we studied functional roles of the endogenous miR-302/367 clu
Externí odkaz:
https://doaj.org/article/013dbb6971ff45629f45dd80125bac16
Autor:
Dinesh, Jaishankar, Cormac, Cosgrove, Prathyaya, Ramesh, James, Mahon, Rohan, Shivde, Emilia R, Dellacecca, Shiayin F, Yang, Jeffrey, Mosenson, José A, Guevara-Patiño, I Caroline, Le Poole
Publikováno v:
Cell Stress Chaperones
Developing immunosuppressive therapies for autoimmune diseases comes with a caveat that immunosuppression may promote the risk of developing other conditions or diseases. We have previously shown that biolistic delivery of an expression construct enc
Publikováno v:
Molecular Therapy. Nucleic Acids
Molecular Therapy: Nucleic Acids, Vol 7, Iss C, Pp 31-41 (2017)
Molecular Therapy: Nucleic Acids, Vol 7, Iss C, Pp 31-41 (2017)
Muscle stem cells (MuSCs) hold great therapeutic potential for muscle genetic disorders, such as Duchenne muscular dystrophy (DMD). The CRISP/Cas9-based genome editing is a promising technology for correcting genetic alterations in mutant genes. In t
Autor:
Xin Wang, Wen Shu Wu, Yalu Zhou, Yuanfan Hong, Jeffrey Mosenson, Furen Wu, Pei Zhu, Gajendra S. Shekhawat
Publikováno v:
Stem Cells Translational Medicine
Muscle stem cells (MuSCs) exhibit robust myogenic potential in vivo, thus providing a promising curative treatment for muscle disorders. Ex vivo expansion of adult MuSCs is highly desired to achieve a therapeutic cell dose because of their scarcity i
Autor:
Yalu Zhou, Pei Zhu, Wen Shu Wu, Yue Sheng, Zhonghui Zhang, Di Xiang, Zhijian Qian, Yuanfan Hong, Jeffrey Mosenson
Publikováno v:
Leukemia
The stem cell factor (SCF)/c-Kit pathway has crucial roles in controlling hematopoietic stem cell (HSC) renewal. However, little is known about the intracellular regulation of the SCF/c-Kit pathway in HSCs. We report here that Slug, a zinc-finger tra
Autor:
Pei Zhu, Jeffrey Mosenson, Wen Li, Elise Wu, Yuanfan Hong, Zhonghui Zhang, Di Xiang, Wen Shu Wu
Publikováno v:
Stem Cell Reports
Stem Cell Reports, Vol 4, Iss 4, Pp 645-657 (2015)
Stem Cell Reports, Vol 4, Iss 4, Pp 645-657 (2015)
Summary miR-302/367 is the most abundant miRNA cluster in human embryonic stem cells (hESCs) and can promote somatic cell reprogramming. However, its role in hESCs remains poorly understood. Here, we studied functional roles of the endogenous miR-302
Publikováno v:
Experimental Dermatology. 22:566-569
Inducible heat-shock protein 70 (HSP70i) is a protein regulated by stress that protects cells from undergoing apoptosis. Such proteins are marvellously well conserved throughout evolution, which has placed them in the spotlight for helping to underst
Autor:
Jeffrey Mosenson, Andrew Zloza, José A. Guevara-Patiño, Jared Klarquist, Allison J. Barfuss, I. Caroline Le Poole
Publikováno v:
Pigment Cell & Melanoma Research. 25:88-98
Summary HSP70i and other stress proteins have been used in anti-tumor vaccines. This begs the question whether HSP70i plays a unique role in immune activation. We vaccinated inducible HSP70i (Hsp70-1) knockout mice and wild-type animals with optimize
Autor:
I. Caroline Le Poole, Michael I. Nishimura, Jonathan M. Eby, Jared Klarquist, B. Jack Longley, Jeffrey Mosenson, Elizabeth Garrett-Mayer, Shikhar Mehrotra, Shilpak Chatterjee, Victor H. Engelhard, Hee Kap Kang
Publikováno v:
Pigment cellmelanoma research. 27(6)
To generate a mouse model of spontaneous epidermal depigmentation, parental h3TA2 mice, expressing both a human-derived, tyrosinase-reactive T-cell receptor on T cells and the matching HLA-A2 transgene, were crossed to keratin 14-promoter driven, ste