Heritability of Nonalcoholic Fatty Liver Disease

Gastroenterology

Volumn 137, Issue 4, 2009, Pages 1536-

  Brouwers, Martijn C G J ^a   van Greevenbroek, Marleen M J ^a   Cantor, Rita M ^b  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; LOW DENSITY LIPOPROTEIN; NEUROPEPTIDE Y;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; CHROMOSOME 1Q; CHROMOSOME 22Q; CHROMOSOME 7P; DYSLIPIDEMIA; FATTY ACID OXIDATION; GENE IDENTIFICATION; GENETIC DISORDER; GENETIC LINKAGE; HERITABILITY; HUMAN; LETTER; LIPID METABOLISM; LIPOGENESIS; NONALCOHOLIC FATTY LIVER; PATHOGENESIS; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; SPECTROSCOPY; BIOPSY; FATTY LIVER; GENETIC SCREENING; GENETICS; LIVER; NOTE; PATHOLOGY; PEDIGREE; RISK FACTOR;

BIOPSY; FATTY LIVER; GENETIC SCREENING; HUMANS; LIVER; PEDIGREE; RISK FACTORS;

EID: 70349414389     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.gastro.2009.03.065     Document Type: Letter

References (4)

1. Schwimmer J.B., Celedon M.A., Lavine J.E., et al. Heritability of nonalcoholic fatty liver disease. Gastroenterology 136 (2009) 1492-1492
2. Brouwers M.C., Cantor R.M., Kono N., et al. Heritability and genetic loci of fatty liver in familial combined hyperlipidemia. J Lipid Res 47 (2006) 2799-2807
3. Mar-Heyming R., Miyazaki M., Weisglas-Volkov D., et al. Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia. Arterioscler Thromb Vasc Biol 28 (2008) 1193-1199
4. van den Hoek A.M., Voshol P.J., Karnekamp B.N., et al. Intracerebroventricular neuropeptide Y infusion precludes inhibition of glucose and VLDL production by insulin. Diabetes 53 (2004) 2529-2534