Format
Sort by
Items per page

Send to

Choose Destination

Links from Protein

Items: 1 to 20 of 51

1.

Differential epigenetic and transcriptional response of the skeletal muscle carnitine palmitoyltransferase 1B (CPT1B) gene to lipid exposure with obesity.

Maples JM, Brault JJ, Witczak CA, Park S, Hubal MJ, Weber TM, Houmard JA, Shewchuk BM.

Am J Physiol Endocrinol Metab. 2015 Aug 15;309(4):E345-56. doi: 10.1152/ajpendo.00505.2014. Epub 2015 Jun 9.

2.

A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome.

Auinger A, Rubin D, Sabandal M, Helwig U, Rüther A, Schreiber S, Foelsch UR, Döring F, Schrezenmeir J.

Br J Nutr. 2013 Mar 14;109(5):810-5. doi: 10.1017/S0007114512002656. Epub 2012 Jul 19.

PMID:
22809552
3.

Exertional rhabdomyolysis: a clinical review with a focus on genetic influences.

Landau ME, Kenney K, Deuster P, Campbell W.

J Clin Neuromuscul Dis. 2012 Mar;13(3):122-36. doi: 10.1097/CND.0b013e31822721ca. Review.

PMID:
22538307
4.

Replacement of C305 in heart/muscle-type isozyme of human carnitine palmitoyltransferase I with aspartic acid and other amino acids.

Matsuo T, Yamamoto A, Yamamoto T, Otsuki K, Yamazaki N, Kataoka M, Terada H, Shinohara Y.

Biochem Genet. 2010 Apr;48(3-4):193-201. doi: 10.1007/s10528-009-9301-z. Epub 2009 Nov 25.

PMID:
19937377
5.

Association of the CPT1B gene with skeletal muscle fat infiltration in Afro-Caribbean men.

Miljkovic I, Yerges LM, Li H, Gordon CL, Goodpaster BH, Kuller LH, Nestlerode CS, Bunker CH, Patrick AL, Wheeler VW, Zmuda JM.

Obesity (Silver Spring). 2009 Jul;17(7):1396-401. doi: 10.1038/oby.2008.677. Epub 2009 Feb 19.

6.

Substitutions of three amino acids in human heart/muscle type carnitine palmitoyltransferase I caused by single nucleotide polymorphisms.

Yamazaki N, Matsuo T, Kurata M, Suzuki M, Fujiwaki T, Yamaguchi S, Terada H, Shinohara Y.

Biochem Genet. 2008 Feb;46(1-2):54-63. Epub 2007 Nov 7.

PMID:
17987377
7.

Cysteine-scanning mutagenesis of muscle carnitine palmitoyltransferase I reveals a single cysteine residue (Cys-305) is important for catalysis.

Liu H, Zheng G, Treber M, Dai J, Woldegiorgis G.

J Biol Chem. 2005 Feb 11;280(6):4524-31. Epub 2004 Dec 3.

8.
9.

Leucine-764 near the extreme C-terminal end of carnitine palmitoyltransferase I is important for activity.

Dai J, Zhu H, Woldegiorgis G.

Biochem Biophys Res Commun. 2003 Feb 14;301(3):758-63.

PMID:
12565845
12.

Functional studies of yeast-expressed human heart muscle carnitine palmitoyltransferase I.

Zhu H, Shi J, de Vries Y, Arvidson DN, Cregg JM, Woldegiorgis G.

Arch Biochem Biophys. 1997 Nov 1;347(1):53-61.

PMID:
9344464
13.

Structural features of the gene encoding human muscle type carnitine palmitoyltransferase I.

Yamazaki N, Yamanaka Y, Hashimoto Y, Shinohara Y, Shima A, Terada H.

FEBS Lett. 1997 Jun 16;409(3):401-6.

14.

Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I.

van der Leij FR, Takens J, van der Veen AY, Terpstra P, Kuipers JR.

Biochim Biophys Acta. 1997 May 30;1352(2):123-8.

PMID:
9199240
15.

Isolation and characterization of cDNA and genomic clones encoding human muscle type carnitine palmitoyltransferase I.

Yamazaki N, Shinohara Y, Shima A, Yamanaka Y, Terada H.

Biochim Biophys Acta. 1996 Jun 7;1307(2):157-61.

PMID:
8679700
16.

Mitochondria-focused gene expression profile reveals common pathways and CPT1B dysregulation in both rodent stress model and human subjects with PTSD.

Zhang L, Li H, Hu X, Benedek DM, Fullerton CS, Forsten RD, Naifeh JA, Li X, Wu H, Benevides KN, Le T, Smerin S, Russell DW, Ursano RJ.

Transl Psychiatry. 2015 Jun 16;5:e580. doi: 10.1038/tp.2015.65.

17.

Carnitine palmitoyltransferase 1B 531K allele carriers sustain a higher respiratory quotient after aerobic exercise, but β3-adrenoceptor 64R allele does not affect lipolysis: a human model.

Gómez-Gómez E, Ríos-Martínez ME, Castro-Rodríguez EM, Del-Toro-Equíhua M, Ramírez-Flores M, Delgado-Enciso I, Pérez-Huitimea AL, Baltazar-Rodríguez LM, Velasco-Pineda G, Muñiz-Murguía J.

PLoS One. 2014 Jun 6;9(6):e96791. doi: 10.1371/journal.pone.0096791. eCollection 2014.

18.

Single nucleotide polymorphism in CPT1B and CPT2 genes and its association with blood carnitine levels in acute myocardial infarction patients.

Khan HA, Alhomida AS.

Gene. 2013 Jul 1;523(1):76-81. doi: 10.1016/j.gene.2013.03.086. Epub 2013 Apr 6.

PMID:
23566841
19.

Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse.

Ji S, You Y, Kerner J, Hoppel CL, Schoeb TR, Chick WS, Hamm DA, Sharer JD, Wood PA.

Mol Genet Metab. 2008 Mar;93(3):314-22. Epub 2007 Nov 19.

20.

Variants within the muscle and liver isoforms of the carnitine palmitoyltransferase I (CPT1) gene interact with fat intake to modulate indices of obesity in French-Canadians.

Robitaille J, Houde A, Lemieux S, Pérusse L, Gaudet D, Vohl MC.

J Mol Med (Berl). 2007 Feb;85(2):129-37. Epub 2006 Nov 7.

PMID:
17089095

Supplemental Content

Support Center