482 related articles for article (PubMed ID: 10706630)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. Giant platelets, megakaryocytes and the expression of glycoprotein Ib-IX complexes.
Nurden P; Nurden A
C R Acad Sci III; 1996 Aug; 319(8):717-26. PubMed ID: 8949396
[TBL] [Abstract][Full Text] [Related]
8. 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; 86(10):3805-14. PubMed ID: 7579348
[TBL] [Abstract][Full Text] [Related]
9. Bernard-Soulier syndrome: quantitative characterization of megakaryocytes and platelets by flow cytometric and platelet kinetic measurements.
Tomer A; Scharf RE; McMillan R; Ruggeri ZM; Harker LA
Eur J Haematol; 1994 Apr; 52(4):193-200. PubMed ID: 8005229
[TBL] [Abstract][Full Text] [Related]
10. Genetic abnormalities of Bernard-Soulier syndrome.
Kunishima S; Kamiya T; Saito H
Int J Hematol; 2002 Nov; 76(4):319-27. PubMed ID: 12463594
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Megakaryocytes derived from patients with the classical form of Bernard-Soulier syndrome show no ability to extend proplatelets in vitro.
Balduini A; Malara A; Balduini CL; Noris P
Platelets; 2011; 22(4):308-11. PubMed ID: 21322749
[No Abstract] [Full Text] [Related]
13. 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]
14. 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; 118(1):260-6. PubMed ID: 12100158
[TBL] [Abstract][Full Text] [Related]
15. Bernard-Soulier syndrome: novel nonsense mutation in GPIbbeta gene affecting GPIb-IX complex expression.
Hadjkacem B; Elleuch H; Gargouri J; Gargouri A
Ann Hematol; 2009 May; 88(5):465-72. PubMed ID: 18825380
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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; 96(2):532-9. PubMed ID: 10887115
[TBL] [Abstract][Full Text] [Related]
18. First Turkish case of Bernard-Soulier syndrome associated with GPIX N45S.
Dağistan N; Kunishima S
Acta Haematol; 2007; 118(3):146-8. PubMed ID: 17804902
[TBL] [Abstract][Full Text] [Related]
19. Patients with Bernard-Soulier syndrome and different severity of the bleeding phenotype.
Boeckelmann D; Hengartner H; Greinacher A; Nowak-Göttl U; Sachs UJ; Peter K; Sandrock-Lang K; Zieger B
Blood Cells Mol Dis; 2017 Sep; 67():69-74. PubMed ID: 28131619
[TBL] [Abstract][Full Text] [Related]
20. Bernard-Soulier syndrome (hemorrhagiparous thrombocytic dystrophy).
Lanza F
Orphanet J Rare Dis; 2006 Nov; 1():46. PubMed ID: 17109744
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
