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Association of a variable number of tandem repeats (VNTR) in glycoprotein Ib alpha and HPA-2 alloantigens.

Simsek S, Bleeker PM, van der Schoot CE, von dem Borne AE.

Thromb Haemost. 1994 Nov;72(5):757-61.


Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region.

Afshar-Kharghan V, Diz-Küçükkaya R, Ludwig EH, Marian AJ, López JA.

Blood. 2001 May 15;97(10):3306-7.


Substitution of Val for Met at residue 239 of platelet glycoprotein Ib alpha in Japanese patients with platelet-type von Willebrand disease.

Takahashi H, Murata M, Moriki T, Anbo H, Furukawa T, Nikkuni K, Shibata A, Handa M, Kawai Y, Watanabe K, et al.

Blood. 1995 Feb 1;85(3):727-33.


The polymorphic integumentary mucin B.1 from Xenopus laevis contains the short consensus repeat.

Probst JC, Hauser F, Joba W, Hoffmann W.

J Biol Chem. 1992 Mar 25;267(9):6310-6.


Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease.

Miller JL, Cunningham D, Lyle VA, Finch CN.

Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4761-5.


MUC3 human intestinal mucin. Analysis of gene structure, the carboxyl terminus, and a novel upstream repetitive region.

Gum JR Jr, Ho JJ, Pratt WS, Hicks JW, Hill AS, Vinall LE, Roberton AM, Swallow DM, Kim YS.

J Biol Chem. 1997 Oct 17;272(42):26678-86.


Molecular modeling of the seven tandem leucine-rich repeats within the ligand-binding region of platelet glycoprotein Ib alpha.

Whisstock JC, Shen Y, López JA, Andrews RK, Berndt MC.

Thromb Haemost. 2002 Feb;87(2):329-33.


Molecular cloning and expression of human tumor-associated polymorphic epithelial mucin.

Gendler SJ, Lancaster CA, Taylor-Papadimitriou J, Duhig T, Peat N, Burchell J, Pemberton L, Lalani EN, Wilson D.

J Biol Chem. 1990 Sep 5;265(25):15286-93.


cDNA for the carboxyl-terminal region of a rat intestinal mucin-like peptide.

Xu G, Huan LJ, Khatri IA, Wang D, Bennick A, Fahim RE, Forstner GG, Forstner JF.

J Biol Chem. 1992 Mar 15;267(8):5401-7.


Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndrome.

Wright SD, Michaelides K, Johnson DJ, West NC, Tuddenham EG.

Blood. 1993 May 1;81(9):2339-47.


Characterization of the gene encoding human platelet glycoprotein IX.

Hickey MJ, Roth GJ.

J Biol Chem. 1993 Feb 15;268(5):3438-43.


The complete cDNA sequence and structural polymorphism of the polypeptide chain of porcine submaxillary mucin.

Eckhardt AE, Timpte CS, DeLuca AW, Hill RL.

J Biol Chem. 1997 Dec 26;272(52):33204-10.


Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome.

Simsek S, Admiraal LG, Modderman PW, van der Schoot CE, von dem Borne AE.

Thromb Haemost. 1994 Sep;72(3):444-9.


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