Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Guocheng He"'
Publikováno v:
ACS Applied Polymer Materials. 4:4949-4960
Publikováno v:
Journal of Clinical Investigation. 117:1078-1087
With-no-lysine (WNK) kinases are a novel family of protein kinases characterized by an atypical placement of the catalytic lysine. Mutations of 2 family members, WNK1 and WNK4, cause pseudohypoaldosteronism type 2 (PHA2), an autosomal-dominant diseas
Autor:
Jason J. Coull, David M. Margolis, Christian Melander, Victor C. Rucker, Peter B. Dervan, Guocheng He
Publikováno v:
Journal of Virology. 76:12349-12354
The host factor LSF represses the human immunodeficiency virus type 1 long terminal repeat (LTR) by mediating recruitment of histone deacetylase. We show that pyrrole-imidazole polyamides targeted to the LTR can specifically block LSF binding both in
Publikováno v:
Journal of Biological Chemistry. 277:44044-44049
Mutations in the phosphotyrosine binding domain protein ARH cause autosomal recessive hypercholesterolemia, a disorder caused by defective internalization of low density lipoprotein receptors (LDLR) in the liver. To examine the function of ARH, we us
Autor:
Guocheng He, David M. Margolis
Publikováno v:
Molecular and Cellular Biology. 22:2965-2973
Biochemical and epigenetic studies have revealed that nucleosomes at eukaryotic promoters function as dynamic units in transcriptional regulation (4, 5, 8, 18, 21, 38, 45). The nucleosome core contains a central histone octamer consisting of four his
Autor:
Theresa A. Grebe, Bing-Zhi Yang, Charles R. Roe, Guocheng He, Diane S. Roe, Kirk Aleck, Roy Teramoto, Jia-Huan Ding
Publikováno v:
Biochemical and Biophysical Research Communications. 264:483-487
Very long chain acyl-CoA dehydrogenase (VLCAD) catalyzes the initial step of long chain fatty acid oxidation in the mitochondria. Patients with VLCAD deficiency have recently been observed with two clinical phenotypes. The cardiac form presents with
Autor:
Bing-Zhi Yang, Jia-Huan Ding, Tracy Dewese, Diane Roe, Guocheng He, Jeff Wilkinson, Donald W. Day, France Demaugre, Daniel Rabier, Michele Brivet, Charles Roe
Publikováno v:
Molecular Genetics and Metabolism. 64:229-236
Carnitine palmitoyltransferase II (CPT II) deficiency, an autosomal recessive disorder of fatty-acid oxidation, presents as three distinct phenotypes (neonatal, infantile, and adult onset). In order to investigate the molecular basis of these three p
Autor:
David M. Margolis, Rupinderjeet Kaur, Ulla Hansen, Holly Johnson, Janet Volker, Loyda Ylisastigui, Guocheng He
Human immunodeficiency virus type 1 (HIV-1) infection is characterized by cycles of virus production and reinfection within activated CD4+ T lymphocytes. The efficiency of HIV-1 replication diminishes as cells enter the resting state, but this lentiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c09be695d6578ee9f7b34b43a8d3988
https://europepmc.org/articles/PMC1091734/
https://europepmc.org/articles/PMC1091734/
Autor:
Guocheng He1, Hao-Ran Wang1, Shao-Kuei Huang1, Chou-Long Huang1 chou-long.huang@utsouthwestern.edu
Publikováno v:
Journal of Clinical Investigation. Apr2007, Vol. 117 Issue 4, p1078. 10p. 1 Color Photograph, 7 Graphs.
Autor:
Ylisastigui, Loyda1, Kaur, Rupinderjeet1, Johnson, Holly1, Volker, Janet2, Guocheng He1, Hansen, Ulla2, Margolis, David1,3 david.margolis@utsouthwestern.edu
Publikováno v:
Journal of Virology. May2005, Vol. 79 Issue 10, p5952-5962. 11p. 8 Diagrams, 1 Chart, 2 Graphs.