Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bipasha Mukherjee-Clavin"'
Autor:
Jonas Van Lent, Robert Prior, Gonzalo Pérez Siles, Anthony N. Cutrupi, Marina L. Kennerson, Tim Vangansewinkel, Esther Wolfs, Bipasha Mukherjee-Clavin, Zachary Nevin, Luke Judge, Bruce Conklin, Henna Tyynismaa, Alex J. Clark, David L. Bennett, Ludo Van Den Bosch, Mario Saporta, Vincent Timmerman
Publikováno v:
Experimental and Molecular Medicine, Vol 56, Iss 6, Pp 1348-1364 (2024)
Abstract Inherited peripheral neuropathies (IPNs) are a group of diseases associated with mutations in various genes with fundamental roles in the development and function of peripheral nerves. Over the past 10 years, significant advances in identify
Externí odkaz:
https://doaj.org/article/ce0749451b9e4264b20443f390aa833e
Autor:
Kathryn R. Moss, Ruifa Mi, Riki Kawaguchi, Jeffrey T. Ehmsen, Qiang Shi, Paula I. Vargas, Bipasha Mukherjee-Clavin, Gabsang Lee, Ahmet Höke
Publikováno v:
iScience, Vol 27, Iss 6, Pp 109855- (2024)
Summary: Establishing robust models of human myelinating Schwann cells is critical for studying peripheral nerve injury and disease. Stem cell differentiation has emerged as a key human cell model and disease motivating development of Schwann cell di
Externí odkaz:
https://doaj.org/article/389891808e4c4e01a9bfaa5738861059
Autor:
Hotae Lim, Shaughn Bell, Kevin Eggan, B.M. Lannon, Young Hyun Che, Barbara Kern, Gabsang Lee, Woochang Hwang, Yohan Oh, Bipasha Mukherjee-Clavin, Junho K. Hur, Omer Habib, Ahmet Hoke, Gerald Brandacher, Ruifa Mi, Kevin J. Kim, Lorenz Studer, Robert H. Baloh, In Young Choi, Yong Jun Kim
Publikováno v:
Nature biomedical engineering
Patient-specific human-induced pluripotent stem cells (hiPSCs) hold great promise for the modelling of genetic disorders. However, these cells display wide intra- and interindividual variations in gene expression, which makes distinguishing true-posi
Publikováno v:
Frontiers in Biology. 8:461-467
Human pluripotent stem cells have been much anticipated as a powerful system to study developmental events, model genetic disorders, and serve as a source of autologous cells for cell therapy in genetic disorders. Precise genetic manipulation is cruc