Ab-sichten. Spaziergang mit Max BeckmannKRAUS, J. P.1986, 102 p.Book

Homocystinuria due to cystathionine β-synthase deficiency: Novel biochemical findings and treatment efficacyORENDAC, M; ZEMAN, J; STABLER, S. P et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 8, pp 761-773, issn 0141-8955, 13 p.Article

The rat MHC and cytathionine β-synthase gene are syntenic on chromosome 20LOCKER, J; GILL, T. J. III; KRAUS, J. P et al.Immunogenetics (New York, NY). 1990, Vol 31, Num 4, pp 271-274, issn 0093-7711Article

Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenaseMATSUBARA, Y; KRAUS, J. P; OZASA, H et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 21, pp 10104-10108, issn 0021-9258Article

Direct DNA sequencing of polymerase chain reaction-amplified genomic DNA by Maxam-Gilbert methodKRAUS, J. P; TAHARA, T.Methods in enzymology. 1993, Vol 218, Num 1, pp 227-233, issn 0076-6879Article

Chaperonin-mediated assembly of wild-type and mutant subunits of human propionyl-CoA carboxylase expressed in Escherichia coliKELSON, T. L; OHURA, T; KRAUS, J. P et al.Human molecular genetics (Print). 1996, Vol 5, Num 3, pp 331-337, issn 0964-6906Article

Variable hyperhomocysteinaemia phenotype in heterozyotes for the Gly307Ser mutation in cystathionine β-synthaseDAWSON, P. A; COCHRAN, D. A. E; EMMERSON, B. T et al.Australian and New Zealand journal of medicine. 1996, Vol 26, Num 2, pp 180-185, issn 0004-8291Conference Paper

Linkage mapping of the cystathionine β-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated regionDMIMITRIOS AVRAMOPOULOS; COX, T; KRAUS, J. P et al.Human genetics. 1993, Vol 90, Num 5, pp 566-568, issn 0340-6717Article

Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiencyWAGSTAFF, J; KORSON, M; KRAUS, J. P et al.The Journal of pediatrics. 1991, Vol 118, Num 4, pp 569-572, issn 0022-3476, 1Article

The gene for cystathionine β-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17MUNKE, M; KRAUS, J. P; OHURA, T et al.American journal of human genetics. 1988, Vol 42, Num 4, pp 550-559, issn 0002-9297Article

Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenaseMATSUBARA, Y; KRAUS, J. P; OZASA, H et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 21, pp 10104-10108, issn 0021-9258Article

RNA required for import of precursor proteins into mitochondriaFIRGAIRA, F. A; HENDRICK, J. P; KALOUSEK, F et al.Science (Washington, D.C.). 1984, Vol 226, Num 4680, pp 1319-1322, issn 0036-8075Article

Mutation analysis in 54 propionic acidemia patientsKRAUS, J. P; SPECTOR, E; WALTER, K et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 1, pp 51-63, issn 0141-8955, 13 p.Article

Reproductive fitness in maternal homocystinuria due to cystathionine β-synthase deficiencyLEVY, H. L; VARGAS, J. E; MACGREGOR, D et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 4, pp 299-314, issn 0141-8955Article

Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223 + 37 del99KOZICH, V; JANOSIK, M; SOKOLOVA, J et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 3, pp 363-366, issn 0141-8955Conference Paper

Genetic maps of mouse chromosome 17 including 12 new anonymous DNA loci and 25 anchor lociNADEAU, J. H; HERRMANN, B; TCHETGEN, M.-B et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 1, pp 78-89, issn 0888-7543, 12 p.Article

Unequal synthesis and differential degradation of propionyl CoA carboxylase subunits in cells from normal and propionic acidemia patientsOHURA, T; KRAUS, J. P; ROSENBERG, L. E et al.American journal of human genetics. 1989, Vol 45, Num 1, pp 33-40, issn 0002-9297Article

Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1MATSUBARA, Y; KRAUS, J. P; YANG-FENG, T. L et al.Proceedings of the National Academy of Sciences of the United States of America. 1986, Vol 83, Num 17, pp 6543-6547, issn 0027-8424Article

A cDNA clone for the precursor of rat mitochondrial ornithine transcarbamylase: comparison of rat and human leader sequences and conservation of catalytic sitesKRAUS, J. P; HODGES, P. E; WILLIAMSON, C. L et al.Nucleic acids research. 1985, Vol 13, Num 3, pp 943-952, issn 0305-1048Article

Biosynthesis and proteolytic activation of cystathionine β-synthase in rat liverSKOVBY, F; KRAUS, J. P; ROSENBERG, L. E et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 1, pp 588-593, issn 0021-9258Article

High incidence of propionic acidemia in Greenland is due to a prevalent mutation, 1540insCCC, in the gene for the β-subunit of propionyl CoA carboxylaseRAVN, K; CHLOUPKOVA, M; CHRISTENSEN, E et al.American journal of human genetics. 2000, Vol 67, Num 1, pp 203-206, issn 0002-9297Article

Is the common 844ins68 polymorphism in the cystathionine β-synthase gene associated with atherosclerosis ?ORENDAC, M; MUSKOVA, B; RICHTEROVA, E et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 5, pp 674-675, issn 0141-8955Article

The molecular basis of cystathionine β-Synthase deficiency in Dutch patients with homocystinuria : Effect of CBS genotype on biochemical and clinical phenotype and on response to treatmentKLUIJTMANS, L. A. J; BOERS, G. H. J; KRAUS, J. P et al.American journal of human genetics. 1999, Vol 65, Num 1, pp 59-67, issn 0002-9297Article

The human cystathionine β-synthase (CBS) gene : Complete sequence, alternative splicing, and polymorphismsKRAUS, J. P; OLIVERIUSOVA, J; PACES, V et al.Genomics (San Diego, Calif.). 1998, Vol 52, Num 3, pp 312-324, issn 0888-7543Article

A missense mutation (1278T) in the cystathionine β-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotypeSHIH, V. E; FRINGER, J. M; MANDELL, R et al.American journal of human genetics. 1995, Vol 57, Num 1, pp 34-39, issn 0002-9297Article