Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Enoch S. E. Tay"'
Autor:
Mosleh Abomughaid, Enoch S. E. Tay, Russell Pickford, Chandra Malladi, Scott A. Read, Jens R. Coorssen, Brian S. Gloss, Jacob George, Mark W. Douglas
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 10; Pages: 8781
The hepatitis C virus (HCV) relies on cellular lipid pathways for virus replication and also induces liver steatosis, but the mechanisms involved are not clear. We performed a quantitative lipidomics analysis of virus-infected cells by combining high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddd281d61cf9dd01fcfc0a6ac5c6e289
Autor:
Sara J. Bontempo, Edna C. Hardeman, Enoch S. E. Tay, Peter W. Gunning, Frances A. Lemckert, Nicole Santucci, Jocelyn Widagdo, Kylie M. Taylor, Stephen J. Palmer, Jeff Hook
Publikováno v:
Journal of Biological Chemistry. 285:4715-4724
The GTF2IRD1 gene is of principal interest to the study of Williams-Beuren syndrome (WBS). This neurodevelopmental disorder results from the hemizygous deletion of a region of chromosome 7q11.23 containing 28 genes including GTF2IRD1. WBS is thought
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc15e30d0e4a51f08d7e41b0026a232
https://doi.org/10.1074/jbc.m109.086660
https://doi.org/10.1074/jbc.m109.086660
Autor:
Patsie Polly, Peter W. Gunning, Edna C. Hardeman, Laura L. Issa, Nanthakumar Subramaniam, Enoch S. E. Tay, Kim L. Guven
Publikováno v:
Biochemical Journal. 374:359-367
A human MusTRD [muscle TFII-I repeat domain (RD)-containing protein] isoform was originally identified in a yeast one-hybrid screen as a protein that binds the slow fibre-specific enhancer of the muscle gene troponin I slow [O'Mahoney, Guven, Lin, Jo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cec3ddde3100d10feee5a83b521a5f7
https://doi.org/10.1042/bj20030189
https://doi.org/10.1042/bj20030189
Autor:
Jeff Hook, Robyn V. Jamieson, Edna C. Hardeman, Thi Thu Cuc Bach, Stephen J. Palmer, Frances A. Lemckert, Peter W. Gunnning, Nicole Santucci, Enoch S. E. Tay
Publikováno v:
Gene expression patterns : GEP. 7(4)
The gene GTF2IRD1 is localized within the critical region on chromosome 7 that is deleted in Williams syndrome patients. Genotype–phenotype comparisons of patients carrying variable deletions within this region have implicated GTF2IRD1 and a closel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a50c6ba9f44fd59e4bc263bcd98ab7
https://pubmed.ncbi.nlm.nih.gov/17239664
https://pubmed.ncbi.nlm.nih.gov/17239664
Autor:
Laura L. Issa, Patsie Polly, Leila M. Haddadi, Nanthakumar Subramaniam, Enoch S. E. Tay, Stephen J. Palmer, Edna C. Hardeman
Publikováno v:
The Journal of biological chemistry. 278(38)
The novel transcription factor hMusTRD1alpha1 (human muscle TFII-I repeat domain-containing protein 1alpha1; previously named MusTRD1; O'Mahoney, J. V., Guven, K. L., Lin, J., Joya, J. E., Robinson, C. S., Wade, R. P., and Hardeman, E. C. (1998) Mol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07fdb5af156671b740145d0a08e7502
https://pubmed.ncbi.nlm.nih.gov/12857748
https://pubmed.ncbi.nlm.nih.gov/12857748