Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Vandana A Gupta"'
Autor:
Arian Mansur, Remi Joseph, Euri S Kim, Pierre M Jean-Beltran, Namrata D Udeshi, Cadence Pearce, Hanjie Jiang, Reina Iwase, Miroslav P Milev, Hashem A Almousa, Elyshia McNamara, Jeffrey Widrick, Claudio Perez, Gianina Ravenscroft, Michael Sacher, Philip A Cole, Steven A Carr, Vandana A Gupta
Publikováno v:
eLife, Vol 12 (2023)
Ubiquitin-proteasome system (UPS) dysfunction is associated with the pathology of a wide range of human diseases, including myopathies and muscular atrophy. However, the mechanistic understanding of specific components of the regulation of protein tu
Externí odkaz:
https://doaj.org/article/e9f154452fff4bc5b183818788e75991
Autor:
Alexis H Bennett, Marie-Francoise O'Donohue, Stacey R Gundry, Aye T Chan, Jeffrey Widrick, Isabelle Draper, Anirban Chakraborty, Yi Zhou, Leonard I Zon, Pierre-Emmanuel Gleizes, Alan H Beggs, Vandana A Gupta
Publikováno v:
PLoS Genetics, Vol 14, Iss 3, p e1007226 (2018)
Gene expression in a tissue-specific context depends on the combined efforts of epigenetic, transcriptional and post-transcriptional processes that lead to the production of specific proteins that are important determinants of cellular identity. Ribo
Externí odkaz:
https://doaj.org/article/aa830dc62bfc4b1c9983f960e31e6328
Autor:
Jeffrey J Widrick, Devin E Gibbs, Benjamin Sanchez, Vandana A Gupta, Anna Pakula, Christian Lawrence, Alan H Beggs, Louis M Kunkel
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199712 (2018)
Zebrafish are a preferred vertebrate model for delineating genotype-phenotype relationships. One of the most studied features of zebrafish is their exceptional swimming ability. By 7 days postfertilization (dpf), zebrafish spend over two-thirds of th
Externí odkaz:
https://doaj.org/article/79f4bb9537e14f62aabe52f35963ee6f
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172648 (2017)
Merosin deficient congenital muscular dystrophy (MDC1A) is a severe neuromuscular disorder with onset in infancy that is associated with severe morbidities (particularly wheelchair dependence) and early mortality. It is caused by recessive mutations
Externí odkaz:
https://doaj.org/article/dcb3c4bdab664b2884ee5d5ab7d23cc4
Autor:
Madhusudan Paul, Prasun Sanyal, Rishmita Mukherjee, Vandana Kumari Gupta, Sneha Bakshi, Avanti Acharya, Trishneeta Bhattacharya, Kunal Chakraborty, Sandip Kumar Mukhopadhyay
Publikováno v:
Oceanologia, Vol 66, Iss 2, Pp 381-393 (2024)
The seasonal reversal of ocean circulation associated with seasonal change in the direction of prevailing winds and the occurrence of several anomalous events in the Eastern Equatorial Indian Ocean (EEIO) make this region dynamic and complex in terms
Externí odkaz:
https://doaj.org/article/50234f2b2e9242ecac95141940beed24
Autor:
Vandana A Gupta, Karim Hnia, Laura L Smith, Stacey R Gundry, Jessica E McIntire, Junko Shimazu, Jessica R Bass, Ethan A Talbot, Leonela Amoasii, Nathaniel E Goldman, Jocelyn Laporte, Alan H Beggs
Publikováno v:
PLoS Genetics, Vol 9, Iss 6, p e1003583 (2013)
X-linked myotubular myopathy (XLMTM) is a congenital disorder caused by mutations of the myotubularin gene, MTM1. Myotubularin belongs to a large family of conserved lipid phosphatases that include both catalytically active and inactive myotubularin-
Externí odkaz:
https://doaj.org/article/86d1bea72b0448b58d06332a5ecc317c
Autor:
Vandana A Gupta, Genri Kawahara, Jennifer A Myers, Aye T Chen, Thomas E Hall, M Chiara Manzini, Peter D Currie, Yi Zhou, Leonard I Zon, Louis M Kunkel, Alan H Beggs
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43794 (2012)
Congenital muscular dystrophy (CMD) is a clinically and genetically heterogeneous group of inherited muscle disorders. In patients, muscle weakness is usually present at or shortly after birth and is progressive in nature. Merosin deficient congenita
Externí odkaz:
https://doaj.org/article/40ee2aaa24de44049e1cbd0ed11f8c8b
Autor:
Muthukumar Karuppasamy, Katherine G. English, Clarissa A. Henry, M. Chiara Manzini, John M. Parant, Melissa A. Wright, Avnika A. Ruparelia, Peter D. Currie, Vandana A. Gupta, James J. Dowling, Lisa Maves, Matthew S. Alexander
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/4f13b14e9c2a4d84a3835d5d9afdf89d
Publikováno v:
Human Molecular Genetics. 32:1711-1721
Nemaline myopathy (NM) is a rare neuromuscular disorder associated with congenital or childhood-onset of skeletal muscle weakness and hypotonia, which results in limited motor function. NM is a genetic disorder and mutations in 12 genes are known to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::678f594c92d738b826b8da8f88d38ab3
https://doi.org/10.1093/hmg/ddad011
https://doi.org/10.1093/hmg/ddad011
Autor:
Natasha Majumder, Monami Dutta, Abhijit Chatterjee, Sneha Bakshi, Prasun Sanyal, Madhusudan Paul, Vandana Kumari Gupta, Avanti Acharya, Sandip Kumar Mukhopadhayay
Publikováno v:
Journal of Atmospheric Chemistry. 80:121-136
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18a90a882bedf01b492e42c63406d4ba
https://doi.org/10.1007/s10874-022-09441-4
https://doi.org/10.1007/s10874-022-09441-4