Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Smriti Agrawal Zaneveld"'
Autor:
Nathaniel Wu, Keqing Wang, Hehe Liu, Yumei Li, Shangyi Fu, Renae Elaine Bertrand, Rui Chen, Jun Wang, Smriti Agrawal Zaneveld, Qingnan Liang
Publikováno v:
Hum Mol Genet
Much of the complexity of the eukaryotic cell transcriptome is due to the alternative splicing of mRNA. However, knowledge on how transcriptome complexity is translated into functional complexity remains limited. For example, although different isofo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7424a45ec012aa2f81e7899c47b282c
https://doi.org/10.1093/hmg/ddab157
https://doi.org/10.1093/hmg/ddab157
Autor:
Kaori Nozawa, Qingnan Liang, Rui Chen, Darius J Devlin, Smriti Agrawal Zaneveld, Xiao Han, Jacob Michael Harnish, Martin M. Matzuk, Abigail R. Moye
Publikováno v:
Biol Reprod
Receptor accessory protein 6 (REEP6) is a member of the REEP/Ypt-interacting protein family that we recently identified as essential for normal endoplasmic reticulum homeostasis and protein trafficking in the retina of mice and humans. Interestingly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da50324f8c98d460ea918649dc277a9d
https://europepmc.org/articles/PMC7253788/
https://europepmc.org/articles/PMC7253788/
Autor:
Keqing Wang, Qingnan Liang, Jacques Zaneveld, Rui Chen, Quynh Nguyen, Smriti Agrawal Zaneveld, Yumei Li, Renae Elaine Bertrand, Nathaniel Wu, Hehe Liu, Aiden Eblimit
Publikováno v:
Human gene therapy. 30(3)
Hereditary retinal dystrophy is clinically defined as a broad group of chronic and progressive disorders that affect visual function by causing photoreceptor degeneration. Previously, we identified mutations in the gene encoding receptor expression-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::639076e84ea5bbec10285f5484a153e1
https://pubmed.ncbi.nlm.nih.gov/30101608
https://pubmed.ncbi.nlm.nih.gov/30101608
Autor:
Wei Liu, Rui Chen, Smriti Agrawal Zaneveld, Kandace Thomas, Aiden Eblimit, Keqing Wang, Yumei Li, Graeme Mardon
NMNAT1 (nicotinamide mononucleotide adenylyltransferase 1) encodes a rate-limiting enzyme that catalyzes the biosynthesis of NAD+ and plays a role in neuroprotection. Mutations in NMNAT1 have been identified to cause a recessive, non-syndromic early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b204002833173689ba477531639bc6a1
https://europepmc.org/articles/PMC6054811/
https://europepmc.org/articles/PMC6054811/