Výsledky vyhledávání - "Caroline Vicanek"

Cloning of a cDNA for Short/Branched Chain Acyl-Coenzyme A Dehydrogenase from Rat and Characterization of Its Tissue Expression and Substrate Specificity

Autor: Kevin P. Battaile, Jerry Vockley, Jan Willard, Rima Rozen, Caroline Vicanek, Paul P. Van Veldhoven, Abdul H. Fauq

Publikováno v: Archives of Biochemistry and Biophysics. 331:127-133

The acyl-CoA dehydrogenases are a family of related enzymes which catalyze the alpha,beta-dehydrogenation of acyl-CoA esters, transferring electrons to electron-transferring flavoprotein. A cDNA for human short/branched chain acyl-CoA dehydrogenase h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b76b2fd1764d8b9c8dd9585f4bde249c
https://doi.org/10.1006/abbi.1996.0290

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Isolation and Expression of a cDNA Encoding the Precursor for a Novel Member (ACADSB) of the Acyl-CoA Dehydrogenase Gene Family

Autor: Caroline Vicanek, Rima Rozen, Katherine Fu, Beatrice Fournier, Elena Torban, Jan Willard, Renate Milos, Lawrence Low-Nang, Jerry Vockley, Lubing Zhou

Publikováno v: Genomics. 24:280-287

The acyl-CoA dehydrogenases (ACDs) are a family of mitochondrial enzymes that oxidize straight chain or branched chain acyl-CoAs in the metabolism of fatty acids or branched chain amino acids. Deficiencies in members of this gene family are important

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e098e430d45f7b1a166bf79fd6189242
https://doi.org/10.1006/geno.1994.1617

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Regulation of renal EGF receptor expression is normal in Denys-Drash syndrome

Autor: Emanuela Ferretti, Jerry Pelletier, Caroline Vicanek, Peter Moffett, Elena Torban, Cynthia G. Goodyer, Paul Goodyer

Publikováno v: Scopus-Elsevier

Regulation of renal EGF receptor expression is normal in Denys-Drash syndrome. In patients with Denys-Drash syndrome, mutations of the Wilms' tumor suppressor gene are associated with nephroblastomas and developmental abnormalities of the genital tra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ed642707b405f4546d38d3631fc086
https://pubmed.ncbi.nlm.nih.gov/9291179

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Transient neonatal cystinuria

Autor: Paul Goodyer, Rima Rozen, Caroline Vicanek, Marylise Boutros

Publikováno v: Kidney International. (2):443-448

Transient neonatal cystinuria.BackgroundCystinuria is an inherited disorder of luminal reabsorptive transport for cystine and dibasic amino acids in the renal proximal tubule. Two cystinuria genes have been identified. Mutations of SLC7A9, which enco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb96266daabceb853e32c309b4d8219a

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