141 related articles for article (PubMed ID: 9622212)
1. Factor X Frankfurt I: molecular and functional characterization of a hereditary factor X deficiency (Gla+25 to Lys).
Nöbauer-Huhmann IM; Höller W; Krinninger B; Turecek PL; Richter G; Scharrer I; Forberg E; Watzke HH
Blood Coagul Fibrinolysis; 1998 Mar; 9(2):143-52. PubMed ID: 9622212
[TBL] [Abstract][Full Text] [Related]
2. The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).
Forberg E; Huhmann I; Jimenez-Boj E; Watzke HH
Thromb Haemost; 2000 Feb; 83(2):234-8. PubMed ID: 10739379
[TBL] [Abstract][Full Text] [Related]
3. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
Chafa O; Tagzirt M; Tapon-Bretaudière J; Reghis A; Fischer AM; LeBonniec BF
Thromb Res; 2009 May; 124(1):144-8. PubMed ID: 19135706
[TBL] [Abstract][Full Text] [Related]
4. Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
Wang WB; Fu QH; Yin J; Wu WM; Ding QL; Zhou RF; Hu YQ; Wang XF; Wang ZY; Wang HL
Haematologica; 2005 Dec; 90(12):1659-64. PubMed ID: 16330440
[TBL] [Abstract][Full Text] [Related]
5. Molecular characterization of two novel mutations causing factor X deficiency in a Chinese pedigree.
Wang WB; Fu QH; Zhou RF; Wu WM; Ding QL; Hu YQ; Wang XF; Wang HL; Wang ZY
Haemophilia; 2005 Jan; 11(1):31-7. PubMed ID: 15660986
[TBL] [Abstract][Full Text] [Related]
6. Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency.
Bereczky Z; Bárdos H; Komáromi I; Kiss C; Haramura G; Ajzner E; Adány R; Muszbek L
Haematologica; 2008 Feb; 93(2):299-302. PubMed ID: 18245654
[TBL] [Abstract][Full Text] [Related]
7. Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively.
Miyata T; Kojima T; Suzuki K; Umeyama H; Yamazaki T; Kamiya T; Toyoda H; Kato H
Thromb Haemost; 1998 Mar; 79(3):486-90. PubMed ID: 9531027
[TBL] [Abstract][Full Text] [Related]
8. Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg").
Watzke HH; Lechner K; Roberts HR; Reddy SV; Welsch DJ; Friedman P; Mahr G; Jagadeeswaran P; Monroe DM; High KA
J Biol Chem; 1990 Jul; 265(20):11982-9. PubMed ID: 1973167
[TBL] [Abstract][Full Text] [Related]
9. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
Al-Hilali A; Wulff K; Abdel-Razeq H; Saud KA; Al-Gaili F; Herrmann FH
Thromb Haemost; 2007 Apr; 97(4):542-5. PubMed ID: 17393015
[TBL] [Abstract][Full Text] [Related]
10. Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency.
Pinotti M; Marchetti G; Baroni M; Cinotti F; Morfini M; Bernardi F
Thromb Haemost; 2002 Aug; 88(2):236-41. PubMed ID: 12195695
[TBL] [Abstract][Full Text] [Related]
11. Protein C Sapporo (protein C Glu 25 --> Lys): a heterozygous missense mutation in the Gla domain provides new insight into the interaction between protein C and endothelial protein C receptor.
Nakabayashi T; Mizukami K; Naitoh S; Takeda M; Shikamoto Y; Nakagawa T; Kaneko H; Tarumi T; Mizoguchi I; Mizuno H; Ieko M; Koike T
Thromb Haemost; 2005 Nov; 94(5):942-50. PubMed ID: 16363234
[TBL] [Abstract][Full Text] [Related]
12. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).
Furlan Freguia C; Toso R; Pollak ES; Arruda VR; Pinotti M; Bernardi F
Haematologica; 2004 Dec; 89(12):1504-9. PubMed ID: 15590402
[TBL] [Abstract][Full Text] [Related]
13. The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.
Girolami A; Allemand E; Scandellari R; Lombardi AM; Girolami B
Hematology; 2009 Jun; 14(3):177-81. PubMed ID: 19490765
[TBL] [Abstract][Full Text] [Related]
14. A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo).
Zama T; Murata M; Watanabe R; Yokoyama K; Moriki T; Ambo H; Murakami H; Kikuchi M; Ikeda Y
Br J Haematol; 1999 Sep; 106(3):809-11. PubMed ID: 10468877
[TBL] [Abstract][Full Text] [Related]
15. [Clotting factor X deficiency resulted from an T 58-->G mutation within exon 1 of human factor X gene].
Yin J; Wang H; Wang X
Zhonghua Xue Ye Xue Za Zhi; 2001 Sep; 22(9):481-3. PubMed ID: 11758231
[TBL] [Abstract][Full Text] [Related]
16. A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency.
Bozzao C; Rimoldi V; Asselta R; Landau M; Ghiotto R; Tenchini ML; De Cristofaro R; Castaman G; Duga S
FEBS J; 2007 Dec; 274(23):6128-38. PubMed ID: 17971173
[TBL] [Abstract][Full Text] [Related]
17. Characterization of recombinant human coagulation factor XFriuli.
Kim DJ; Girolami A; James HL
Thromb Haemost; 1996 Feb; 75(2):313-7. PubMed ID: 8815583
[TBL] [Abstract][Full Text] [Related]
18. Factor X Shanghai: a mutation disrupting translocation to the endoplasmic reticulum.
Asselta R
Haematologica; 2005 Dec; 90(12):1590. PubMed ID: 16330428
[No Abstract] [Full Text] [Related]
19. Factor X Stockton: a mild bleeding diathesis associated with an active site mutation in factor X.
Messier TL; Wong CY; Bovill EG; Long GL; Church WR
Blood Coagul Fibrinolysis; 1996 Jan; 7(1):5-14. PubMed ID: 8845463
[TBL] [Abstract][Full Text] [Related]
20. Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X.
Isshiki I; Favier R; Moriki T; Uchida T; Ishihara H; Van Dreden P; Murata M; Ikeda Y
Blood Coagul Fibrinolysis; 2005 Jan; 16(1):9-16. PubMed ID: 15650540
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]