Author

R. P. Cox

Observed names: R P Cox, R. P. COX, R.P. Cox, RodyP. Cox

Observed institutions: Roswell Park Comprehensive Cancer Center, New York State Department of Health, United States Department of Veterans Affairs, Memorial Sloan Kettering Cancer Center, University of Wisconsin–Madison, Emory University, Veterans Health Administration, NYU Langone Health, Louis Stokes Cleveland VA Medical Center, James J. Peters VA Medical Center, New York University, Case Western Reserve University, The University of Texas Southwestern Medical Center

OpenAlex ID: A5111476094

A study of adenosine 3′:5′-cyclic monophosphate, sodium butyrate and cortisol as inducers of HeLa alkaline phosphatase

1974 · M.J. Griffin, G.H. Price, et al. · Archives of Biochemistry and Biophysics · 116

Familial hyperlysinemias. Purification and characterization of the bifunctional aminoadipic semialdehyde synthase with lysine-ketoglutarate reductase and saccharopine dehydrogenase activities.

1984 · P J Markovitz, D T Chuang, et al. · Journal of Biological Chemistry · 87

Molecular Phenotypes in Cultured Maple Syrup Urine Disease Cells

1989 · C W Fisher, J L Chuang, et al. · Journal of Biological Chemistry · 68

Complementation Analysis of Maple Syrup Urine Disease in Heterokaryons derived from Cultured Human Fibroblasts

1973 · LINDA B. LYONS, R. P. COX, et al. · Nature · 53

Isolation and sequencing of a cDNA encoding the decarboxylase (E1)alpha precursor of bovine branched-chain alpha-keto acid dehydrogenase complex. Expression of E1 alpha mRNA and subunit in maple-syrup-urine-disease and 3T3-L1 cells.

1988 · C W Hu, K S Lau, et al. · Journal of Biological Chemistry · 46

Tocopherol and the Stability of Carotene

1942 · F.W. Quackenbush, R.P. Cox, et al. · Journal of Biological Chemistry · 45

Effect of simple sugars on the morphology and growth pattern of mammalian cell cultures.

1965 · R P Cox, B M Gesner · Proceedings of the National Academy of Sciences · 43

Maple syrup urine disease in Mennonites. Evidence that the Y393N mutation in E1 alpha impedes assembly of the E1 component of branched-chain alpha-keto acid dehydrogenase complex.

1991 · C R Fisher, J L Chuang, et al. · Journal of Clinical Investigation · 42

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Activities of branched-chain 2-oxo acid dehydrogenase and its components in skin fibroblasts from normal and classical-maple-syrup-urine-disease subjects

1981 · D T Chuang, W L Niu, et al. · Biochemical Journal · 42

Catalytic and structural properties of the dihydrolipoyl transacylase component of bovine branched-chain alpha-keto acid dehydrogenase.

1984 · D T Chuang, C C Hu, et al. · Journal of Biological Chemistry · 40

Thiamin-responsive maple-syrup-urine disease: decreased affinity of the mutant branched-chain alpha-keto acid dehydrogenase for alpha-ketoisovalerate and thiamin pyrophosphate.

1982 · D T Chuang, L S Ku, et al. · Proceedings of the National Academy of Sciences · 36

In-utero Detection of Pompe's Disease

1970 · RodyP. Cox, Gordon Douglas, et al. · The Lancet · 36

Subunit structure of the dihydrolipoyl transacylase component of branched-chain alpha-keto acid dehydrogenase complex from bovine liver. Characterization of the inner transacylase core.

1985 · D T Chuang, C W Hu, et al. · Journal of Biological Chemistry · 35

Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients.

1995 · J L Chuang, J R Davie, et al. · Journal of Clinical Investigation · 34

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Hypoxanthine phosphoribosyltransferase activity in intact fibroblasts from patients with X-linked hyperuricemia.

1976 · M J Holland, A M DiLorenzo, et al. · Journal of Clinical Investigation · 33

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Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology.

1979 · J Dancis, J Hutzler, et al. · Europe PMC (PubMed Central) · 31

Studies on cell communication with enucleated human fibroblasts.

1976 · R P Cox, M R Krauss, et al. · The Journal of Cell Biology · 31

Structure of the gene encoding dihydrolipoyl transacylase (E2) component of human branched chain alpha-keto acid dehydrogenase complex and characterization of an E2 pseudogene.

1992 · K.S. Lau, W.J. Herring, et al. · Journal of Biological Chemistry · 29

A Chemical Method for the Isolation of H E L a Cell Nuclei and the Nuclear Localization of H E L a Cell Alkaline Phosphatase

1967 · M. J. Griffin, R. P. Cox, et al. · The Journal of Cell Biology · 28

E2 transacylase-deficient (type II) maple syrup urine disease. Aberrant splicing of E2 mRNA caused by internal intronic deletions and association with thiamine-responsive phenotype.

1997 · J L Chuang, R P Cox, et al. · Journal of Clinical Investigation · 26

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Ultrastructural and enzymic modulation of hela cells induced by sodium butyrate and the effects of cytochalasin b and colcemid

1976 · S. I. Deutsch, D. N. Silvers, et al. · Journal of Cell Science · 25

Maple syrup urine disease: branched-chain keto acid decarboxylation in fibroblasts as measured with amino acids and keto acids.

1977 · J Dancis, J Hutzler, et al. · Europe PMC (PubMed Central) · 24

Subunit structure of the dihydrolipoyl transacylase component of branched-chain alpha-keto acid dehydrogenase complex from bovine liver. Mapping of the lipoyl-bearing domain by limited proteolysis.

1986 · C W Hu, T A Griffin, et al. · Journal of Biological Chemistry · 21

Detection of heterozygotes in maple-syrup-urine disease: measurements of branched-chain alpha-ketoacid dehydrogenase and its components in cell cultures.

1982 · D T Chuang, L S Ku, et al. · PubMed · 21

Incorporation of hypoxanthine by PHA-stimulated HPRT-deficient lymphocytes

1974 · R.P. Cox, M.R. Krauss, et al. · Experimental Cell Research · 14

Works count: 45

Citation count: 1,063

H-index: 22

I10-index: 26