Zobrazeno 1 - 10
of 1 244
pro vyhledávání: '"Lin, V"'
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-18 (2023)
Abstract Background CD-1 is an outbred mouse stock that is frequently used in toxicology, pharmacology, and fundamental biomedical research. Although inbred strains are typically better suited for such studies due to minimal genetic variability, outb
Externí odkaz:
https://doaj.org/article/09779d1438674ca8ba3c0692f49e57dc
Akademický článek
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Autor:
Jung, Yoon Hee1 (AUTHOR), Wang, Hsiao-Lin V.1 (AUTHOR), Ali, Samir2 (AUTHOR), Corces, Victor G.1 (AUTHOR), Kremsky, Isaac2,3 (AUTHOR) ikremsky@llu.edu
Publikováno v:
BMC Genomics. 8/4/2023, Vol. 24 Issue 1, p1-18. 18p.
Autor:
Silvia Amor-Barris, Helle Høyer, Lin V. Brauteset, Els De Vriendt, Linda Strand, Albena Jordanova, Geir J. Braathen, Kristien Peeters
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background Autosomal recessive axonal neuropathy with neuromyotonia has been linked to loss of functional HINT1. The disease is particularly prevalent in Central and South-East Europe, Turkey and Russia due to the high carrier frequency of t
Externí odkaz:
https://doaj.org/article/5077f8bf7710478fb6e064768da3d973
Autor:
Hannah Gabriela Valverde de Morales, Hsiao‐Lin V. Wang, Kathryn Garber, Xiaodong Cheng, Victor G. Corces, Hong Li
Publikováno v:
American Journal of Medical Genetics Part A. 191:718-729
Monoallelic variants of CTCF cause an autosomal dominant neurodevelopmental disorder with a wide range of features, including impacts on the brain, growth, and craniofacial development. A growing number of subjects with CTCF-related disorder (CRD) ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e5759e3a142479cee5e4ccf158789b3
https://doi.org/10.1002/ajmg.a.63065
https://doi.org/10.1002/ajmg.a.63065
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
In Policy and Society September-December 2015 34(3-4):229-245
Autor:
Hsiao-Lin V. Wang, Austin M. Veire, Tania F. Gendron, Marla Gearing, Jonathan D. Glass, Peng Jin, Victor G. Corces, Zachary T. McEachin
Repeat expansions in theC9orf72gene are the most common genetic cause of amyotrophic lateral sclerosis and familial frontotemporal dementia (ALS/FTD). To identify molecular defects that take place in the dorsolateral frontal cortex of patients withC9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9126d2b86f1b92603661ef0cd2f9b156
https://doi.org/10.1101/2023.01.12.523820
https://doi.org/10.1101/2023.01.12.523820
Autor:
Wang, Hsiao-Lin V., Corces, Victor G.
Publikováno v:
Mol Cell
Two recent reports (Martinez-Ara et al., 2022; Bergman et al., 2022) explore the compatibility between enhancers and promoters and find that enhancers preferentially activate promoters with low intrinsic activity rather than favoring housekeeping or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aede37c181fb32bd854bae8064e14320
https://doi.org/10.1016/j.molcel.2022.06.014
https://doi.org/10.1016/j.molcel.2022.06.014
Autor:
Shaira Marie J. Castillo, Day Bert R. Mariñas, Roberto R. Coloma, Lin V. Tadeja, Katherine D. Tan, Frederick F. Patacsil
Publikováno v:
International Journal of Information Engineering and Electronic Business. 13:9-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9f50d11e768f9a88122c2341087abc2
https://doi.org/10.5815/ijieeb.2021.05.02
https://doi.org/10.5815/ijieeb.2021.05.02