These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
188 related items for PubMed ID: 9639514
1. Naturally occurring mutations in glycoprotein Ibalpha that result in defective ligand binding and synthesis of a truncated protein. Kenny D, Jónsson OG, Morateck PA, Montgomery RR. Blood; 1998 Jul 01; 92(1):175-83. PubMed ID: 9639514 [Abstract] [Full Text] [Related]
2. The critical interaction of glycoprotein (GP) IBbeta with GPIX-a genetic cause of Bernard-Soulier syndrome. Kenny D, Morateck PA, Gill JC, Montgomery RR. Blood; 1999 May 01; 93(9):2968-75. PubMed ID: 10216092 [Abstract] [Full Text] [Related]
4. Surface expression of glycoprotein ib alpha is dependent on glycoprotein ib beta: evidence from a novel mutation causing Bernard-Soulier syndrome. Moran N, Morateck PA, Deering A, Ryan M, Montgomery RR, Fitzgerald DJ, Kenny D. Blood; 2000 Jul 15; 96(2):532-9. PubMed ID: 10887115 [Abstract] [Full Text] [Related]
5. A dinucleotide deletion results in defective membrane anchoring and circulating soluble glycoprotein Ib alpha in a novel form of Bernard-Soulier syndrome. Kenny D, Newman PJ, Morateck PA, Montgomery RR. Blood; 1997 Oct 01; 90(7):2626-33. PubMed ID: 9326229 [Abstract] [Full Text] [Related]
7. A novel missense mutation shows that GPIbbeta has a dual role in controlling the processing and stability of the platelet GPIb-IX adhesion receptor. Strassel C, Pasquet JM, Alessi MC, Juhan-Vague I, Chambost H, Combrié R, Nurden P, Bas MJ, De La Salle C, Cazenave JP, Lanza F, Nurden AT. Biochemistry; 2003 Apr 22; 42(15):4452-62. PubMed ID: 12693941 [Abstract] [Full Text] [Related]
8. Compound heterozygosity of the GPIbalpha gene associated with Bernard-Soulier syndrome. González-Manchón C, Larrucea S, Pastor AL, Butta N, Arias-Salgado EG, Ayuso MS, Parrilla R. Thromb Haemost; 2001 Dec 22; 86(6):1385-91. PubMed ID: 11776304 [Abstract] [Full Text] [Related]
9. A Leu7Pro mutation in the signal peptide of platelet glycoprotein (GP)IX in a case of Bernard-Soulier syndrome abolishes surface expression of the GPIb-V-IX complex. Lanza F, De La Salle C, Baas MJ, Schwartz A, Boval B, Cazenave JP, Caen JP. Br J Haematol; 2002 Jul 22; 118(1):260-6. PubMed ID: 12100158 [Abstract] [Full Text] [Related]
10. Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome. Kunishima S, Matsushita T, Ito T, Kamiya T, Saito H. Am J Hematol; 2002 Dec 22; 71(4):279-84. PubMed ID: 12447957 [Abstract] [Full Text] [Related]
11. Disruption of the Cys5-Cys7 disulfide bridge in the platelet glycoprotein Ibbeta prevents the normal maturation and surface exposure of GPIb-IX complexes. González-Manchón C, Butta N, Iruín G, Alonso S, Ayuso MS, Parrilla R. Thromb Haemost; 2003 Sep 22; 90(3):456-64. PubMed ID: 12958615 [Abstract] [Full Text] [Related]
12. The genetic defect in two well-studied cases of Bernard-Soulier syndrome: a point mutation in the fifth leucine-rich repeat of platelet glycoprotein Ib alpha. Li C, Martin SE, Roth GJ. Blood; 1995 Nov 15; 86(10):3805-14. PubMed ID: 7579348 [Abstract] [Full Text] [Related]
13. Platelets with a W127X mutation in GPIX express sufficient residual amounts of GPIbα to support adhesion to von Willebrand factor and collagen. Takata Y, Kanaji T, Moroi M, Seki R, Sano M, Nakazato S, Sueoka E, Imamura Y, Okamura T. Int J Hematol; 2012 Dec 15; 96(6):733-42. PubMed ID: 23143686 [Abstract] [Full Text] [Related]
14. Novel Bernard-Soulier syndrome variants caused by compound heterozygous mutations (case I) or a cytoplasmic tail truncation (case II) of GPIbα. Yamamoto N, Akamatsu N, Sakuraba H, Matsuno K, Hosoya R, Nogami H, Kasahara K, Mitsuyama S, Arai M. Thromb Res; 2013 Apr 15; 131(4):e160-7. PubMed ID: 23414566 [Abstract] [Full Text] [Related]
15. Glycoprotein (GP) Ib-IX-transfected cells roll on a von Willebrand factor matrix under flow. Importance of the GPib/actin-binding protein (ABP-280) interaction in maintaining adhesion under high shear. Cranmer SL, Ulsemer P, Cooke BM, Salem HH, de la Salle C, Lanza F, Jackson SP. J Biol Chem; 1999 Mar 05; 274(10):6097-106. PubMed ID: 10037692 [Abstract] [Full Text] [Related]
16. A novel homozygous 8-base pair deletion mutation in the glycoprotein Ibalpha gene in a patient with Bernard-Soulier syndrome. Imai C, Kunishima S, Takachi T, Iwabuchi H, Nemoto T, Imamura M, Uchiyama M. Blood Coagul Fibrinolysis; 2009 Sep 05; 20(6):470-4. PubMed ID: 19448529 [Abstract] [Full Text] [Related]
17. The membrane-proximal intermolecular disulfide bonds in glycoprotein Ib influence receptor binding to von Willebrand factor. Mo X, Luo SZ, Munday AD, Sun W, Berndt MC, López JA, Dong JF, Li R. J Thromb Haemost; 2008 Oct 05; 6(10):1789-95. PubMed ID: 18647229 [Abstract] [Full Text] [Related]
18. Cytoplasmic domains of GpIbalpha and GpIbbeta regulate 14-3-3zeta binding to GpIb/IX/V. Feng S, Christodoulides N, Reséndiz JC, Berndt MC, Kroll MH. Blood; 2000 Jan 15; 95(2):551-7. PubMed ID: 10627461 [Abstract] [Full Text] [Related]
19. The glycoprotein Ibalpha-von Willebrand factor interaction induces platelet apoptosis. Li S, Wang Z, Liao Y, Zhang W, Shi Q, Yan R, Ruan C, Dai K. J Thromb Haemost; 2010 Feb 15; 8(2):341-50. PubMed ID: 19840363 [Abstract] [Full Text] [Related]
20. Identification of a novel 14-3-3zeta binding site within the cytoplasmic domain of platelet glycoprotein Ibalpha that plays a key role in regulating the von Willebrand factor binding function of glycoprotein Ib-IX. Yuan Y, Zhang W, Yan R, Liao Y, Zhao L, Ruan C, Du X, Dai K. Circ Res; 2009 Dec 04; 105(12):1177-85. PubMed ID: 19875727 [Abstract] [Full Text] [Related] Page: [Next] [New Search]