J. Metherall

发表

Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndrome.

P. Patel, K. Ferrell, P. Das, 1999, American journal of medical genetics.

Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing β‐Thalassemia a

F. Collins, S. Weissman, E. Feingold, 1985, Annals of the New York Academy of Sciences.

Loss of transcriptional repression of three sterol-regulated genes in mutant hamster cells.

M. Brown, J. Goldstein, K. Luskey, 1989, The Journal of biological chemistry.

A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries.

D. Grunwald, K. Hoshijima, J. Metherall, 2002, Genes & development.

Progesterone Inhibits Cholesterol Biosynthesis in Cultured Cells

J. Metherall, K. Waugh, Huijuan Li, 1996, The Journal of Biological Chemistry.

Role for sterol regulatory element binding protein in the regulation of farnesyl diphosphate synthase and in the control of cellular levels of cholesterol and triglyceride: evidence from sterol regulation-defective cells.

P. Edwards, S. Jackson, J. Ericsson, 1996, Journal of lipid research.

Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.

F. Collins, S. Weissman, B. Forget, 1986, The EMBO journal.

Cholesterol Metabolism Regulation

Elizabeth A. Nash, J. Metherall, Darren C Warnick, 2005 .

Loss of transcriptional activation of three sterol-regulated genes in mutant hamster cells

M. Evans, J. Metherall, 1993, Molecular and cellular biology.

A 25-hydroxycholesterol-resistant cell line deficient in acyl-CoA: cholesterol acyltransferase.

P. Dawson, N. Ridgway, M. Brown, 1991, The Journal of biological chemistry.

Genetic distinction between sterol-mediated transcriptional and posttranscriptional control of 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

P. Dawson, N. Ridgway, M. Brown, 1991, The Journal of biological chemistry.

Expression cloning of a diphtheria toxin receptor: Identity with a heparin-binding EGF-like growth factor precursor

D. Russell, J. Naglich, Leon Eidels, 1992, Cell.

Role of Multidrug Resistance P-glycoproteins in Cholesterol Biosynthesis (*)

H. Li, J. Metherall, K. Waugh, 1996, The Journal of Biological Chemistry.

Biochemical variants of Smith-Lemli-Opitz syndrome.

D. Neklason, R. Kelley, J. Metherall, 1999, American journal of medical genetics.

Analyses of linked beta-globin genes suggest that nondeletion forms of hereditary persistence of fetal hemoglobin are bona fide switching mutants.

B. Forget, F. Gillespie, J. Metherall, 1988, American journal of human genetics.

Identification of casein kinase I substrates by in vitro expression cloning screening.

D. Virshup, J. Metherall, Z. H. Gao, 2000, Biochemical and biophysical research communications.

GENETIC BASIS OF DISTAL ARTHROGRYPOSES

M. Bamshad, A. Moon, R. Toydemir, 2012 .

Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin

S. Weissman, C. Stoeckert, B. Forget, 1987, Molecular and cellular biology.

Images in clinical medicine. Sarcoidosis.

J. Metherall, E. Oates, 1993, The New England journal of medicine.

Role of Multidrug Resistance P-glycoproteins in Cholesterol Esterification*

Elizabeth A. Nash, D. Neklason, P. Debry, 1997, The Journal of Biological Chemistry.

scylla and charybde, homologues of the human apoptotic gene RTP801, are required for head involution in Drosophila.

A. Letsou, K. Simin, J. Metherall, 2006, Developmental biology.

A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin

F. Collins, S. Weissman, B. Forget, 1985, Nature.

Profiling patterned transcripts in Drosophila embryos.

R. Weiss, D. Dunn, A. Letsou, 2002, Genome research.

The Growth Requirements of Vertebrate Cells in Vitro

J. Metherall, 1982, The Yale Journal of Biology and Medicine.

UV-induced DNA-binding proteins in human cells.

P. Glazer, W. Summers, N. Greggio, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Analyses of Linked P-Globin Genes Suggest That Nondeletion Forms of Hereditary Persistence of Fetal Hemoglobin Are Bona Fide Switching Mutants

J. Metherall, B. G. Forget, F. P. Gillespie, 2006 .