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Items: 7

1.

Vps33b is crucial for structural and functional hepatocyte polarity.

Hanley J, Dhar DK, Mazzacuva F, Fiadeiro R, Burden JJ, Lyne AM, Smith H, Straatman-Iwanowska A, Banushi B, Virasami A, Mills K, Lemaigre FP, Knisely AS, Howe S, Sebire N, Waddington SN, Paulusma CC, Clayton P, Gissen P.

J Hepatol. 2017 May;66(5):1001-1011. doi: 10.1016/j.jhep.2017.01.001. Epub 2017 Jan 9.

2.

The Role of Platelets and ε-Aminocaproic Acid in Arthrogryposis, Renal Dysfunction, and Cholestasis (ARC) Syndrome Associated Hemorrhage.

Weyand AC, Lombel RM, Pipe SW, Shavit JA.

Pediatr Blood Cancer. 2016 Mar;63(3):561-3. doi: 10.1002/pbc.25814. Epub 2015 Oct 27.

3.

Characterization of a Novel Integrin Binding Protein, VPS33B, Which Is Important for Platelet Activation and In Vivo Thrombosis and Hemostasis.

Xiang B, Zhang G, Ye S, Zhang R, Huang C, Liu J, Tao M, Ruan C, Smyth SS, Whiteheart SW, Li Z.

Circulation. 2015 Dec 15;132(24):2334-44. doi: 10.1161/CIRCULATIONAHA.115.018361. Epub 2015 Sep 23.

4.

Current Strategies in Diagnosis of Inherited Storage Pool Defects.

Sandrock K, Zieger B.

Transfus Med Hemother. 2010;37(5):248-258. Epub 2010 Sep 15.

5.

Genetics of familial intrahepatic cholestasis syndromes.

van Mil SW, Houwen RH, Klomp LW.

J Med Genet. 2005 Jun;42(6):449-63. Review.

7.

Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis syndrome.

Saraiva JM, Mota HC.

J Med Genet. 1994 Oct;31(10):820. No abstract available.

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