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Items: 8


Role of genetic changes in the progression of cardiovascular diseases.

Sheweita SA, Baghdadi H, Allam AR.

Int J Biomed Sci. 2011 Dec;7(4):238-48.


Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22.

Wang X, Li X, Zhang YB, Zhang F, Sun L, Lin J, Wang DM, Wang LY.

PLoS One. 2011;6(10):e24838. doi: 10.1371/journal.pone.0024838.


Familial hypercholesterolemia: the lipids or the genes?

Fahed AC, Nemer GM.

Nutr Metab (Lond). 2011 Apr 22;8(1):23. doi: 10.1186/1743-7075-8-23.


The AP-2 adaptor beta2 appendage scaffolds alternate cargo endocytosis.

Keyel PA, Thieman JR, Roth R, Erkan E, Everett ET, Watkins SC, Heuser JE, Traub LM.

Mol Biol Cell. 2008 Dec;19(12):5309-26. doi: 10.1091/mbc.E08-07-0712.


Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemia.

Jones C, Garuti R, Michaely P, Li WP, Maeda N, Cohen JC, Herz J, Hobbs HH.

J Clin Invest. 2007 Jan;117(1):165-74.


A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.

Puppala S, Dodd GD, Fowler S, Arya R, Schneider J, Farook VS, Granato R, Dyer TD, Almasy L, Jenkinson CP, Diehl AK, Stern MP, Blangero J, Duggirala R.

Am J Hum Genet. 2006 Mar;78(3):377-92.


Restoration of LDL receptor function in cells from patients with autosomal recessive hypercholesterolemia by retroviral expression of ARH1.

Eden ER, Patel DD, Sun XM, Burden JJ, Themis M, Edwards M, Lee P, Neuwirth C, Naoumova RP, Soutar AK.

J Clin Invest. 2002 Dec;110(11):1695-702.

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