Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysis.

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Genomics

• Publication date

  1994-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1006/GENO.1994.1264PMID 8088809
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Assignment of the gene for the core protein II (UQCRC2) subunit of the mitochondrial cytochrome bc1 complex to human chromosome 16p12.

  1993cited by this paper
• Pork and human cDNAs encoding glutaryl-CoA dehydrogenase.

  1992cited by this paper
• The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7

  1989cited by this paper
• The purification and characterization of glutaryl-coenzyme A dehydrogenase from porcine and human liver.

  1986cited by this paper
• The gene for clotting factor 10 is mapped to 13q32----qter.

  1986cited by this paper
• High-resolution chromosomal localization of the beta-gene of the human beta-globin gene complex by in situ hybridization.

  1985cited by this paper
• Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor

  1985cited by this paper

• Disorders of organic acid metabolism and epilepsy

  2024cites this paper
• Glutaric Acid Neurotoxicity: Mechanisms and Actions

  2021cites this paper
• Glutaric Acidemia, Pathogenesis and Nutritional Therapy

  2021cites this paper
• Clinical and mutational spectrum of 4 Chinese families with glutaric aciduria type 1

  2019cites this paper
• Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation

  2018cites this paper
• Mistakes are not an option: a clinical case of glutaric aciduria type 1

  2018cites this paper
• A novel variant of the GCDH gene causes glutaric aciduria type 1 in a Sudanese family: a case report -

  2017cites this paper
• Glutaric acidemia (type I)

  2017cites this paper
• GAI - distinct genotype and phenotype characteristics in reported Slovak patients.

  2016cites this paper
• Clinical and Mutational Analysis of the GCDH Gene in Malaysian Patients with Glutaric Aciduria Type 1

  2016cites this paper
• Batwing appearance – A neuroradiologic clue to glutaric aciduria-type 1

  2015cites this paper
• A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I

  2015cites this paper
• Newborn Screening for Glutaric Aciduria Type I: Benefits and limitations

  2015cites this paper
• Molecular analysis of Cypriot patients with Glutaric aciduria type I: identification of two novel mutations.

  2014cites this paper
• A Case of Glutaric Aciduria Type I with a Novel Mutation

  2013cites this paper
• Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade of experience.

  2012cites this paper
• Glutaric aciduria type I: A translational approach to an enigmatic disease

  2011cites this paper
• Therapeutic modulation of cerebral L-lysine metabolism in a mouse model for glutaric aciduria type I.

  2011cites this paper
• ‹ki tarafl› temporal araknoid kistler ve glütarik asidüri tip 1 Bilateral temporal arachnoid cysts and glutaric aciduria type 1

  2008cites this paper
• Early detection of glutaric aciduria type I by newborn screening in Taiwan.

  2008cites this paper
• [Glutaric aciduria type I. Clinical, biochemical and molecular findings in six patients in Venezuela].

  2007cites this paper
• Untersuchungen zu in vitro und und in vivo (Mus musculus Linneaus., 1758) Effekten von 3-Hydroxyglutarsäure

  2006cites this paper
• Cerebral 1H MR spectroscopy revealing white matter NAA decreases in glutaric aciduria type I.

  2006cites this paper
• Efeito do ácido glutárico sobre parâmetros do sistema glutamatérgico em cérebro de ratos ao longo do desenvolvimento

  2006cites this paper
• Riboflavin-responsive glutaryl CoA dehydrogenase deficiency.

  2006cites this paper
• [Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age].

  2005cites this paper
• Diagnosis of glutaric acidemia type I: A cautionary note

  2005cites this paper
• Glutaric aciduria type 1 in a Kuwaiti infant.

  2004cites this paper
• Vestibulitis, Kopfschmerzen, Makrozephalie

  2004cites this paper
• Glutaric aciduria type I and kynurenine pathway metabolites: A modified hypothesis

  2004cites this paper
• Pathomechanisms of neurodegeneration in glutaryl‐CoA dehydrogenase deficiency

  2004cites this paper
• Glutaryl-CoA Dehydrogenase Deficiency: Region-Specific Analysis of Organic Acids and Acylcarnitines in post mortem Brain Predicts Vulnerability of the Putamen

  2003cites this paper
• Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

  2003cites this paper
• Ca2+ and Na+ Dependence of 3-Hydroxyglutarate-Induced Excitotoxicity in Primary Neuronal Cultures from Chick Embryo Telencephalons

  2002cites this paper
• Ca(2+) and Na(+) dependence of 3-hydroxyglutarate-induced excitotoxicity in primary neuronal cultures from chick embryo telencephalons.

  2002cites this paper
• Glutaryl‐CoA Dehydrogenase

  2002cites this paper
• A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay

  2002cites this paper
• Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

  2002cites this paper
• Intrastriatal administration of 3-hydroxyglutaric acid induces convulsions and striatal lesions in rats.

  2001cites this paper
• Ocular findings in glutaric aciduria type 1.

  2000cites this paper
• Prenatal molecular diagnosis of glutaric aciduria type I by direct mutation analysis

  2000cites this paper
• Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

  2000cites this paper
• Isolation and characterization of the gene encoding the mouse broad specificity lysosomal alpha-mannosidase1.

  1999cites this paper
• Glutaryl‐CoA dehydrogenase mutations in glutaric acidemia (type I): Review and report of thirty novel mutations

  1998cites this paper
• Novel mutations of the glutaryl-CoA dehydrogenase gene in two Japanese patients with glutaric aciduria type I.

  1998cites this paper
• The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type I

  1998influential citation
• Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions

  1997cites this paper
• Early clinical manifestation of glutaric aciduria type I and nephrotic syndrome during the first months of life

  1997cites this paper
• Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish.

  1996cites this paper
• Genetic mapping and embryonic expression of a novel, maternally transcribed gene Mem3

  1996cites this paper
• Glutaric aciduria type I in the Arab and Jewish communities in Israel.

  1996cites this paper
• A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type I.

  1995cites this paper
• Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene.

  1995cites this paper