Citations for
1CD36, CD36D
Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol.
Love-Gregory L, Sherva R, Sun L, Wasson J, Schappe T, Doria A, Rao DC, Hunt SC, Klein S, Neuman RJ, Permutt MA, Abumrad NA.
Hum Mol Genet 17(11):1695-704. Epub 2008 Feb 27. 2008
2CD36, CD36D
Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension.
Pravenec M, Churchill PC, Churchill MC, Viklicky O, Kazdova L, Aitman TJ, Petretto E, Hubner N, Wallace CA, Zimdahl H, Zidek V, Landa V, Dunbar J, Bidani A, Griffin K, Qi N, Maxova M, Kren V, Mlejnek P, Wang J, Kurtz TW.
Nat Genet 40(8):952-4. Epub 2008 Jun 29. 2008
3CD36, CD36D
CD36 is important for fatty acid and cholesterol uptake by the proximal but not distal intestine.
Nassir F, Wilson B, Han X, Gross RW, Abumrad NA.
J Biol Chem 282(27):19493-501. Epub 2007 May 15. 2007
4CD36, CD36D
Attenuated aerobic exercise capacity in CD36 deficiency.
Yanai H, Watanabe I, Ishii K, Morimoto M, Fujiwara H, Yoshida S, Hui SP, Matsuno K, Chiba H.
J Med Genet 44(7):445-7. Epub 2007 Apr 5. 2007
5CD36, CD36D
CD36 is a receptor for oxidized high density lipoprotein: implications for the development of atherosclerosis.
Thorne RF, Mhaidat NM, Ralston KJ, Burns GF.
FEBS Lett 581(6):1227-32. Epub 2007 Feb 28. 2007
6CD36, CD36D
Importance of the carboxyl terminus of FAT/CD36 for plasma membrane localization and function in long-chain fatty acid uptake.
Eyre NS, Cleland LG, Tandon NN, Mayrhofer G.
J Lipid Res 48(3):528-42. Epub 2006 Dec 1. 2007
7CD36, CD36D
CD36 deficiency rescues lipotoxic cardiomyopathy.
Yang J, Sambandam N, Han X, Gross RW, Courtois M, Kovacs A, Febbraio M, Finck BN, Kelly DP.
Circ Res 100(8):1208-17. Epub 2007 Mar 15. 2007
8CD36, CD36D
Molecular basis of the Cd36 chromosomal deletion underlying SHR defects in insulin action and fatty acid metabolism.
Glazier AM, Scott J, Aitman TJ.
Mamm Genome 13(2):108-13. 2002
9CD36, CD36D
Analyses of genetic abnormalities in type I CD36 deficiency in Japan: identification and cell biological characterization of two novel mutations that cause CD36 deficiency in man.
Kashiwagi H, Tomiyama Y, Nozaki S, Kiyoi T, Tadokoro S, Matsumoto K, Honda S, Kosugi S, Kurata Y, Matsuzawa Y.
Hum Genet 108(6):459-66. 2001
10CD36, CD36D
Molecular basis of CD36 deficiency. Evidence that a 478C-T substitution (proline90-serine) in CD36 cDNA accounts for CD36 deficiency.
Kashiwagi H, et al.
J Clin Invest 95 : 1040-1046. 1995
11CD36, CD36D
Identification of molecular defects in a subject with type I CD36 deficiency.
Kashiwagi H, et al.
Blood 83 : 3545-3552. 1994