scully, an essential gene of Drosophila, is homologous to mammalian mitochondrial type II L-3-hydroxyacyl-CoA dehydrogenase/amyloid-beta peptide-binding protein
about
Comparative evolutionary genomics of the HADH2 gene encoding Abeta-binding alcohol dehydrogenase/17beta-hydroxysteroid dehydrogenase type 10 (ABAD/HSD10)Expanded substrate screenings of human and Drosophila type 10 17beta-hydroxysteroid dehydrogenases (HSDs) reveal multiple specificities in bile acid and steroid hormone metabolism: characterization of multifunctional 3alpha/7alpha/7beta/17beta/20betHuman brain short chain L-3-hydroxyacyl coenzyme A dehydrogenase is a single-domain multifunctional enzyme. Characterization of a novel 17beta-hydroxysteroid dehydrogenaseMyxococcus CsgA, Drosophila Sniffer, and human HSD10 are cardiolipin phospholipasesCoordinated metabolic transitions during Drosophila embryogenesis and the onset of aerobic glycolysis.Prodos is a conserved transcriptional regulator that interacts with dTAF(II)16 in Drosophila melanogaster.Enigma, a mitochondrial protein affecting lifespan and oxidative stress response in Drosophila.Mitochondrial dysfunction and Alzheimer's disease: role of amyloid-beta peptide alcohol dehydrogenase (ABAD).Pathogenic role of mitochondrial [correction of mitochondral] amyloid-beta peptide.Loss of the mitochondrial protein-only ribonuclease P complex causes aberrant tRNA processing and lethality in Drosophila.HSD10 disease: clinical consequences of mutations in the HSD17B10 gene.Lipid metabolism and Drosophila sperm development.Short-chain dehydrogenase/reductase (SDR) relationships: a large family with eight clusters common to human, animal, and plant genomes.The SIN3 deacetylase complex represses genes encoding mitochondrial proteins: implications for the regulation of energy metabolism.Methods for studying the metabolic basis of Drosophila development.Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex.Mutations of the withered (whd) gene in Drosophila melanogaster confer hypersensitivity to oxidative stress and are lesions of the carnitine palmitoyltransferase I (CPT I) gene.2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease.Levels of 17β-Hydroxysteroid Dehydrogenase Type 10 in Cerebrospinal Fluid of People with Mild Cognitive Impairment and Various Types of Dementias.
P2860
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P2860
scully, an essential gene of Drosophila, is homologous to mammalian mitochondrial type II L-3-hydroxyacyl-CoA dehydrogenase/amyloid-beta peptide-binding protein
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
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1998年學術文章
@zh-hant
name
scully, an essential gene of D ...... d-beta peptide-binding protein
@ast
scully, an essential gene of D ...... d-beta peptide-binding protein
@en
type
label
scully, an essential gene of D ...... d-beta peptide-binding protein
@ast
scully, an essential gene of D ...... d-beta peptide-binding protein
@en
prefLabel
scully, an essential gene of D ...... d-beta peptide-binding protein
@ast
scully, an essential gene of D ...... d-beta peptide-binding protein
@en
P2093
P2860
P356
P1476
scully, an essential gene of D ...... d-beta peptide-binding protein
@en
P2093
B Hämmerle
D Ortuño-Sahagún
J A Barbas
P2860
P304
P356
10.1083/JCB.141.4.1009
P407
P577
1998-05-01T00:00:00Z