202 related articles for article (PubMed ID: 15213102)
1. Genetic deletion of mouse platelet glycoprotein Ibbeta produces a Bernard-Soulier phenotype with increased alpha-granule size.
Kato K; Martinez C; Russell S; Nurden P; Nurden A; Fiering S; Ware J
Blood; 2004 Oct; 104(8):2339-44. PubMed ID: 15213102
[TBL] [Abstract][Full Text] [Related]
2. Generation and rescue of a murine model of platelet dysfunction: the Bernard-Soulier syndrome.
Ware J; Russell S; Ruggeri ZM
Proc Natl Acad Sci U S A; 2000 Mar; 97(6):2803-8. PubMed ID: 10706630
[TBL] [Abstract][Full Text] [Related]
3. Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.
Bartsch I; Sandrock K; Lanza F; Nurden P; Hainmann I; Pavlova A; Greinacher A; Tacke U; Barth M; Busse A; Oldenburg J; Bommer M; Strahm B; Superti-Furga A; Zieger B
Thromb Haemost; 2011 Sep; 106(3):475-83. PubMed ID: 21800012
[TBL] [Abstract][Full Text] [Related]
4. Lentiviral gene rescue of a Bernard-Soulier mouse model to study platelet glycoprotein Ibβ function.
Strassel C; Bull A; Moog S; Receveur N; Mallo L; Mangin P; Eckly A; Freund M; Dubart-Kupperschmitt A; Gachet C; Lanza F
J Thromb Haemost; 2016 Jul; 14(7):1470-9. PubMed ID: 27148783
[TBL] [Abstract][Full Text] [Related]
5. Amelioration of the macrothrombocytopenia associated with the murine Bernard-Soulier syndrome.
Kanaji T; Russell S; Ware J
Blood; 2002 Sep; 100(6):2102-7. PubMed ID: 12200373
[TBL] [Abstract][Full Text] [Related]
6. Hemizygosity for the gene encoding glycoprotein Ibβ is not responsible for macrothrombocytopenia and bleeding in patients with 22q11 deletion syndrome.
Zwifelhofer NMJ; Bercovitz RS; Weik LA; Moroi A; LaRose S; Newman PJ; Newman DK
J Thromb Haemost; 2019 Feb; 17(2):295-305. PubMed ID: 30549403
[TBL] [Abstract][Full Text] [Related]
7. A novel hemizygous Bernard-Soulier Syndrome (BSS) mutation in the amino terminal domain of glycoprotein (GP)Ibbeta--platelet characterization and transfection studies.
Hillmann A; Nurden A; Nurden P; Combrié R; Claeyssens S; Moran N; Kenny D
Thromb Haemost; 2002 Dec; 88(6):1026-32. PubMed ID: 12529755
[TBL] [Abstract][Full Text] [Related]
8. Decreased thrombotic tendency in mouse models of the Bernard-Soulier syndrome.
Strassel C; Nonne C; Eckly A; David T; Leon C; Freund M; Cazenave JP; Gachet C; Lanza F
Arterioscler Thromb Vasc Biol; 2007 Jan; 27(1):241-7. PubMed ID: 17095718
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.
Kunishima S; Sako M; Yamazaki T; Hamaguchi M; Saito H
Eur J Haematol; 2006 Dec; 77(6):501-12. PubMed ID: 16978236
[TBL] [Abstract][Full Text] [Related]
10. Bernard-soulier syndrome with a homozygous 13 base pair deletion in the signal peptide-coding region of the platelet glycoprotein Ib(beta) gene.
Watanabe R; Ishibashi T; Saitoh Y; Shichishima T; Maruyama Y; Enomoto Y; Handa M; Oda A; Ambo H; Murata M; Ikeda Y
Blood Coagul Fibrinolysis; 2003 Jun; 14(4):387-94. PubMed ID: 12945881
[TBL] [Abstract][Full Text] [Related]
11. Molecular characterization of two mutations in platelet glycoprotein (GP) Ib alpha in two Finnish Bernard-Soulier syndrome families.
Koskela S; Partanen J; Salmi TT; Kekomäki R
Eur J Haematol; 1999 Mar; 62(3):160-8. PubMed ID: 10089893
[TBL] [Abstract][Full Text] [Related]
12. Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated Finnish families.
Koskela S; Javela K; Jouppila J; Juvonen E; Nyblom O; Partanen J; Kekomäki R
Eur J Haematol; 1999 Apr; 62(4):256-64. PubMed ID: 10227459
[TBL] [Abstract][Full Text] [Related]
13. Bernard-Soulier syndrome caused by a dinucleotide deletion and reading frameshift in the region encoding the glycoprotein Ib alpha transmembrane domain.
Afshar-Kharghan V; López JA
Blood; 1997 Oct; 90(7):2634-43. PubMed ID: 9326230
[TBL] [Abstract][Full Text] [Related]
14. 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; 93(9):2968-75. PubMed ID: 10216092
[TBL] [Abstract][Full Text] [Related]
15. A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibbeta gene affects GPIb/IX complex expression--Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form.
Kurokawa Y; Ishida F; Kamijo T; Kunishima S; Kenny D; Kitano K; Koike K
Thromb Haemost; 2001 Nov; 86(5):1249-56. PubMed ID: 11816714
[TBL] [Abstract][Full Text] [Related]
16. Bernard-Soulier syndrome due to compound heterozygosity for a novel glycoprotein Ibβ mutation.
Sato T; Kunishima S; Shirayama R; Ichikawa S; Sakai M; Kusuhara K
Acta Haematol; 2014; 131(1):46-9. PubMed ID: 24051937
[No Abstract] [Full Text] [Related]
17. Synthesis, assembly, and intracellular transport of the platelet glycoprotein Ib-IX-V complex.
Dong JF; Gao S; López JA
J Biol Chem; 1998 Nov; 273(47):31449-54. PubMed ID: 9813057
[TBL] [Abstract][Full Text] [Related]
18. A three-base deletion removing a leucine residue in a leucine-rich repeat of platelet glycoprotein Ib alpha associated with a variant of Bernard-Soulier syndrome (Nancy I).
de la Salle C; Baas MJ; Lanza F; Schwartz A; Hanau D; Chevalier J; Gachet C; Briquel ME; Cazenave JP
Br J Haematol; 1995 Feb; 89(2):386-96. PubMed ID: 7873390
[TBL] [Abstract][Full Text] [Related]
19. Bernard-Soulier syndrome with severe bleeding: absent platelet glycoprotein Ib alpha due to a homozygous one-base deletion.
Li C; Pasquale DN; Roth GJ
Thromb Haemost; 1996 Nov; 76(5):670-4. PubMed ID: 8950770
[TBL] [Abstract][Full Text] [Related]
20. Intrinsic impaired proplatelet formation and microtubule coil assembly of megakaryocytes in a mouse model of Bernard-Soulier syndrome.
Strassel C; Eckly A; Léon C; Petitjean C; Freund M; Cazenave JP; Gachet C; Lanza F
Haematologica; 2009 Jun; 94(6):800-10. PubMed ID: 19377075
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]