These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 17065362)

  • 1. The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility: the DAMAGE study.
    van Hove EC; Hansen T; Dekker JM; Reiling E; Nijpels G; Jørgensen T; Borch-Johnsen K; Hamid YH; Heine RJ; Pedersen O; Maassen JA; 't Hart LM
    Diabetes; 2006 Nov; 55(11):3193-6. PubMed ID: 17065362
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Short-chain 3-hydroxyacyl-CoA dehydrogenase is a negative regulator of insulin secretion in response to fuel and non-fuel stimuli in INS832/13 β-cells.
    Pepin E; Guay C; Delghingaro-Augusto V; Joly E; Madiraju SR; Prentki M
    J Diabetes; 2010 Sep; 2(3):157-67. PubMed ID: 20923481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structural organization of the human short-chain L-3-hydroxyacyl-CoA dehydrogenase gene.
    Vredendaal PJ; van den Berg IE; Stroobants AK; van der A DL; Malingré HE; Berger R
    Mamm Genome; 1998 Sep; 9(9):763-8. PubMed ID: 9716664
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitro.
    Velasco K; St-Louis JL; Hovland HN; Thompson N; Ottesen Å; Choi MH; Pedersen L; Njølstad PR; Arnesen T; Fjeld K; Aukrust I; Myklebust LM; Molven A
    J Inherit Metab Dis; 2021 Jan; 44(1):240-252. PubMed ID: 32876354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
    Clayton PT; Eaton S; Aynsley-Green A; Edginton M; Hussain K; Krywawych S; Datta V; Malingre HE; Berger R; van den Berg IE
    J Clin Invest; 2001 Aug; 108(3):457-65. PubMed ID: 11489939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Specificity in beta cell expression of L-3-hydroxyacyl-CoA dehydrogenase, short chain, and potential role in down-regulating insulin release.
    Martens GA; Vervoort A; Van de Casteele M; Stangé G; Hellemans K; Van Thi HV; Schuit F; Pipeleers D
    J Biol Chem; 2007 Jul; 282(29):21134-44. PubMed ID: 17491019
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?
    Eaton S; Chatziandreou I; Krywawych S; Pen S; Clayton PT; Hussain K
    Biochem Soc Trans; 2003 Dec; 31(Pt 6):1137-9. PubMed ID: 14641012
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
    Li C; Chen P; Palladino A; Narayan S; Russell LK; Sayed S; Xiong G; Chen J; Stokes D; Butt YM; Jones PM; Collins HW; Cohen NA; Cohen AS; Nissim I; Smith TJ; Strauss AW; Matschinsky FM; Bennett MJ; Stanley CA
    J Biol Chem; 2010 Oct; 285(41):31806-18. PubMed ID: 20670938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.
    Molven A; Matre GE; Duran M; Wanders RJ; Rishaug U; Njølstad PR; Jellum E; Søvik O
    Diabetes; 2004 Jan; 53(1):221-7. PubMed ID: 14693719
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene.
    Hussain K; Clayton PT; Krywawych S; Chatziandreou I; Mills P; Ginbey DW; Geboers AJ; Berger R; van den Berg IE; Eaton S
    J Pediatr; 2005 May; 146(5):706-8. PubMed ID: 15870679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism.
    Zhang W; Sang YM
    Orphanet J Rare Dis; 2021 Nov; 16(1):467. PubMed ID: 34736508
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease.
    Yang SY; He XY; Schulz H
    FEBS J; 2005 Oct; 272(19):4874-83. PubMed ID: 16176262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase.
    Bennett MJ; Russell LK; Tokunaga C; Narayan SB; Tan L; Seegmiller A; Boriack RL; Strauss AW
    Mol Genet Metab; 2006; 89(1-2):74-9. PubMed ID: 16725361
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human short-chain L-3-hydroxyacyl-CoA dehydrogenase: cloning and characterization of the coding sequence.
    Vredendaal PJ; van den Berg IE; Malingré HE; Stroobants AK; Olde Weghuis DE; Berger R
    Biochem Biophys Res Commun; 1996 Jun; 223(3):718-23. PubMed ID: 8687463
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel insights into fatty acid oxidation, amino acid metabolism, and insulin secretion from studying patients with loss of function mutations in 3-hydroxyacyl-CoA dehydrogenase.
    Heslegrave AJ; Hussain K
    J Clin Endocrinol Metab; 2013 Feb; 98(2):496-501. PubMed ID: 23253615
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder.
    He XY; Yang SY
    Mol Genet Metab; 2007 Jun; 91(2):205-6. PubMed ID: 17434778
    [No Abstract]   [Full Text] [Related]  

  • 17. Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase.
    Heslegrave AJ; Kapoor RR; Eaton S; Chadefaux B; Akcay T; Simsek E; Flanagan SE; Ellard S; Hussain K
    Orphanet J Rare Dis; 2012 May; 7():25. PubMed ID: 22583614
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Short-chain 3-hydroxyacyl-coenzyme A dehydrogenase associates with a protein super-complex integrating multiple metabolic pathways.
    Narayan SB; Master SR; Sireci AN; Bierl C; Stanley PE; Li C; Stanley CA; Bennett MJ
    PLoS One; 2012; 7(4):e35048. PubMed ID: 22496890
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Intrinsic alcohol dehydrogenase and hydroxysteroid dehydrogenase activities of human mitochondrial short-chain L-3-hydroxyacyl-CoA dehydrogenase.
    He XY; Yang YZ; Schulz H; Yang SY
    Biochem J; 2000 Jan; 345 Pt 1(Pt 1):139-43. PubMed ID: 10600649
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deficiency of the metabolic enzyme SCHAD in pancreatic β-cells promotes amino acid-sensitive hypoglycemia.
    St-Louis JL; El Jellas K; Velasco K; Slipp BA; Hu J; Helgeland G; Steine SJ; De Jesus DF; Kulkarni RN; Molven A
    J Biol Chem; 2023 Aug; 299(8):104986. PubMed ID: 37392854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.