Hyperketotic states due to inherited defects of ketolysis.
about
Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patientObligate role for ketone body oxidation in neonatal metabolic homeostasisCardiomyocyte-specific deficiency of ketone body metabolism promotes accelerated pathological remodeling.Ketone body metabolism and cardiovascular diseaseHyperketonemia and ketosis increase the risk of complications in type 1 diabetes.An insight into the biochemistry of inborn errors of metabolism for a clinical neurologist.Multi-dimensional Roles of Ketone Bodies in Fuel Metabolism, Signaling, and Therapeutics.
P2860
Q24315007-8F533E39-E6A2-48F6-8356-87B085BD5145Q28505766-8419AA15-74B6-42B9-B9D4-D61239EA71F8Q34404106-636B1BF8-403F-4138-9F49-B51DA96650BCQ36764435-A30DDECA-DEA4-41F5-BC14-39057DE27E57Q36901925-302A1A87-7645-4EB0-8263-8C68D93D0F4EQ37409037-6B35D8EA-EA07-4B31-AF09-FAF9EC307462Q39126658-1306CF91-9A5E-4872-84B5-E73F2287505E
P2860
Hyperketotic states due to inherited defects of ketolysis.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Hyperketotic states due to inherited defects of ketolysis.
@en
Hyperketotic states due to inherited defects of ketolysis.
@nl
type
label
Hyperketotic states due to inherited defects of ketolysis.
@en
Hyperketotic states due to inherited defects of ketolysis.
@nl
prefLabel
Hyperketotic states due to inherited defects of ketolysis.
@en
Hyperketotic states due to inherited defects of ketolysis.
@nl
P2093
P1433
P1476
Hyperketotic states due to inherited defects of ketolysis.
@en
P2093
Bonnefont JP
Charpentier C
Middleton B
Saudubray JM
Vassault A
P577
1987-01-01T00:00:00Z