Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jitendra K. Kanaujiya"'
Autor:
Jitendra K. Kanaujiya, Jay S. Mishra
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/8c04c5e456e640b0be2a4bc5aaa13d5b
Publikováno v:
Cell Reprogram
Differentiation of keratinocytes from human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) has become an important tool for wound healing research and for studying skin diseases in instances where patient cells are not
Publikováno v:
Blood. 138:1085-1085
De novo generation of hematopoietic stem cells (HSCs) from human induced pluripotent stem cells (hiPSCs) could provide a virtually unlimited supply of autologous HSCs for clinical transplantation, and offer various approaches that enable gene therapy
Publikováno v:
Pharmaceutical Patent Analyst. 6:115-134
Unlike with zinc finger nuclease and transcriptional activator-like effector nuclease DNA modification technologies that rely on lead proteins, developed through expensive and time-consuming processes, the clustered regularly interspaced short palind
Autor:
Ernst J Reichenberger, Jitendra K Kanaujiya, Mark Hochstrasser, Edward Bastow, I-Ping Chen, Zhifang Hao, Raj Luxmi, Dimitrios Zattas
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Mutations in the progressive ankylosis protein (NP_473368, human ANKH) cause craniometaphyseal dysplasia (CMD), characterized by progressive thickening of craniofacial bones and widened metaphyses in long bones. The pathogenesis of CMD remains largel
Autor:
Victoria Odesina, Ernst J Reichenberger, Regie Lyn P. Santos-Cortez, Deborah A. Nickerson, Suzanne M. Leal, Fairouz Benahmed-Miniuk, Fanyue Sun, SA Ademola, Ying Hu, P.B. Olaitan, Solomon Olufemi Fadiora, Odunayo M Oluwatosin, Michael J. Bamshad, Jitendra K Kanaujiya, Jian Tao
Keloids result from abnormal proliferative scar formation with scar tissue expanding beyond the margin of the original wound and are mostly found in individuals of sub-Saharan African descent. The etiology of keloids has not been resolved but previou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3bc780b540c69b0c21c045217da61e
https://europepmc.org/articles/PMC5602022/
https://europepmc.org/articles/PMC5602022/
Publikováno v:
Stem Cell Reports
Stem Cell Reports, Vol 9, Iss 5, Pp 1369-1376 (2017)
Stem Cell Reports, Vol 9, Iss 5, Pp 1369-1376 (2017)
Summary We identified osteoclast defects in craniometaphyseal dysplasia (CMD) using an easy-to-use protocol for differentiating osteoclasts from human induced pluripotent stem cells (hiPSCs). CMD is a rare genetic bone disorder, characterized by life