Purification of low-abundance messenger RNAs from rat liver by polysome immunoadsorption.

Por Kraus, J P, Rosenberg, L E
Publicado em 1982

An unusual insertion/deletion in the gene encoding the beta-subunit of propionyl-CoA carboxylase is a frequent mutation in Caucasian propionic acidemia.

Por Tahara, T, Kraus, J P, Rosenberg, L E
Publicado em 1990

Unequal synthesis and differential degradation of propionyl CoA carboxylase subunits in cells from normal and propionic acidemia patients.

Por Ohura, T, Kraus, J P, Rosenberg, L E
Publicado em 1989

Homocystinuria: biogenesis of cystathionine beta-synthase subunits in cultured fibroblasts and in an in vitro translation system programmed with fibroblast messenger RNA.

Por Skovby, F, Kraus, J P, Rosenberg, L E
Publicado em 1984

The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

Por Münke, M, Kraus, J P, Ohura, T, Francke, U
Publicado em 1988

Evidence for the evolutionary origin of human chromosome 21 from comparative gene mapping in the cow and mouse.

Por Threadgill, D S, Kraus, J P, Krawetz, S A, Womack, J E
Publicado em 1991

Different structures in the amino-terminal domain of the ornithine transcarbamylase leader peptide are involved in mitochondrial import and carboxyl-terminal cleavage.

Por Kraus, J P, Novotný, J, Kalousek, F, Swaroop, M, Rosenberg, L E
Publicado em 1988

Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.

Por Fenton, W A, Hack, A M, Kraus, J P, Rosenberg, L E
Publicado em 1987

Molecular cloning of the cDNA coding for rat ornithine transcarbamoylase.

Por Horwich, A L, Kraus, J P, Williams, K, Kalousek, F, Konigsberg, W, Rosenberg, L E
Publicado em 1983

Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1.

Por Matsubara, Y, Kraus, J P, Yang-Feng, T L, Francke, U, Rosenberg, L E, Tanaka, K
Publicado em 1986

The molecular basis of homocystinuria due to cystathionine beta-synthase deficiency in Italian families, and report of four novel mutations.

Por Sebastio, G, Sperandeo, M P, Panico, M, de Franchis, R, Kraus, J P, Andria, G
Publicado em 1995

Coding sequence of the precursor of the beta subunit of rat propionyl-CoA carboxylase.

Por Kraus, J P, Firgaira, F, Novotný, J, Kalousek, F, Williams, K R, Williamson, C, Ohura, T, Rosenberg, L E
Publicado em 1986

Cloning and screening with nanogram amounts of immunopurified mRNAs: cDNA cloning and chromosomal mapping of cystathionine beta-synthase and the beta subunit of propionyl-CoA carbo...

Por Kraus, J P, Williamson, C L, Firgaira, F A, Yang-Feng, T L, Münke, M, Francke, U, Rosenberg, L E
Publicado em 1986

A cDNA clone for the precursor of rat mitochondrial ornithine transcarbamylase: comparison of rat and human leader sequences and conservation of catalytic sites.

Por Kraus, J P, Hodges, P E, Williamson, C L, Horwich, A L, Kalousek, F, Williams, K R, Rosenberg, L E
Publicado em 1985

The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to...

Por Kluijtmans, L A, Boers, G H, Kraus, J P, van den Heuvel, L P, Cruysberg, J R, Trijbels, F J, Blom, H J
Publicado em 1999

A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotype.

Por Shih, V E, Fringer, J M, Mandell, R, Kraus, J P, Berry, G T, Heidenreich, R A, Korson, M S, Levy, H L, Ramesh, V
Publicado em 1995

Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.

Por Kluijtmans, L A, Boers, G H, Stevens, E M, Renier, W O, Kraus, J P, Trijbels, F J, van den Heuvel, L P, Blom, H J
Publicado em 1996