Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Vijay V Vishnu"'
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102900- (2022)
An Embryonic stem line was engineered with CRISPR mediated knock-in to tag the endogenous locus of Sox2 with tdTomato and Gata6 with GFP. The site-specific knock-ins were genotyped by PCR and DNA sequencing. The timely expression of Gata6 and loss of
Externí odkaz:
https://doaj.org/article/81c454e63edf4fad851172106f61f489
Autor:
Vijayishwer S. Jamwal, Vijay V. Vishnu, Anusha Domreddy, Yash Parekh, Bokara Kiran Kumar, P. Chandra Shekar, Shashi Singh
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101963- (2020)
An integration free iPSC line was generated from fibroblast obtained from the skin of an aborted fetus in feeder free conditions using episomal based vectors expressing the pluripotency factors. The cell line generated was characterized and tested fo
Externí odkaz:
https://doaj.org/article/ed6d5fc68e4b471daf599c1ff7a54e82
Autor:
Debabrata Jana, Priya Singh, Purnima Sailasree, Mansi Srivast, Nithyapriya Kumar, Vijay V Vishnu, Hanuman T Kale, Jyothi Lakshmi, Gunda Srini, Divya Tej Sowpati, P Chandra Shekar
Mouse epiblast and embryonic stem cells (mESCs) are considered to adhere strict lineage restriction and lack the potential to contribute to trophoectoderm (TE). In contrast, here we report the derivation of trophoblast stem cells (ESTS) from the mESC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64293250c4067e3707b68403a5fe24f4
https://doi.org/10.21203/rs.3.rs-2882798/v1
https://doi.org/10.21203/rs.3.rs-2882798/v1
Autor:
Debabrata Jana, Purnima Sailasree, Priya Singh, Mansi Srivastava, Vijay V Vishnu, Hanuman T Kale, Jyothi Lakshmi, Gunda Srinivas, Divya Tej Sowpati, P Chandra Shekar
SUMMARYmESCs and epiblast are considered to follow strict lineage adherence and lack the potential to contribute to trophoectoderm. Here, we report the derivation of trophoblast stem cells (ESTS) from the mESCs. The single-cell transcriptome and mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d8d09eafcf96583ffd27b9d08c5d66a
https://doi.org/10.1101/2023.04.19.537518
https://doi.org/10.1101/2023.04.19.537518
Autor:
Debabrata Jana, Priya Singh, Purnima Sailasree, Nithyapriya Kumar, Vijay V Vishnu, Hanuman T Kale, Jyothi Lakshmi, Asha Kumari, Divya Tej Sowpati, P Chandra Shekar
SummaryHuman pluripotent stem cells (hPSCs) can self-organize into a blastocyst-like structure (blastoid) by virtue of their full developmental potential. The pluripotent mouse embryonic stem cells (mESC) are considered to lack this potential and hen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1ca18d51dc120af26ec7274815ffc1
https://doi.org/10.1101/2023.04.12.536583
https://doi.org/10.1101/2023.04.12.536583
A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics
Autor:
Hanuman T Kale, Rajendra Singh Rajpurohit, Debabrata Jana, Vijay V Vishnu, Mansi Srivastava, Preeti R Mourya, Gunda Srinivas, P Chandra Shekar
Publikováno v:
EMBO reports. 23(11)
The self-renewal and differentiation potential of embryonic stem cells (ESCs) is maintained by the regulated expression of core pluripotency factors. Expression levels of the core pluripotency factor Nanog are tightly regulated by a negative feedback
Autor:
Divya Tej Sowpati, Vijay V. Vishnu, Archana Verma, Bh Muralikrishna, P. Chandra Shekar, Sanjeev Chavan Nayak, Vegesna Radha
Publikováno v:
Stem Cell Reviews and Reports
Graphical abstract C3G (RAPGEF1), engaged in multiple signaling pathways, is essential for the early development of the mouse. In this study, we have examined its role in mouse embryonic stem cell self-renewal and differentiation. C3G null cells gene
Autor:
Anusha Domreddy, Vijayishwer S. Jamwal, P. Chandra Shekar, Vijay V. Vishnu, Bokara Kiran Kumar, Shashi Singh, Yash Parekh
Publikováno v:
Stem Cell Research, Vol 48, Iss, Pp 101963-(2020)
An integration free iPSC line was generated from fibroblast obtained from the skin of an aborted fetus in feeder free conditions using episomal based vectors expressing the pluripotency factors. The cell line generated was characterized and tested fo