236 related articles for article (PubMed ID: 31185295)
21. N-glycan-dependent quality control of the Na,K-ATPase beta(2) subunit.
Tokhtaeva E; Munson K; Sachs G; Vagin O
Biochemistry; 2010 Apr; 49(14):3116-28. PubMed ID: 20199105
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Factor VII deficiency caused by a structural variant N57D of the first epidermal growth factor domain.
Leonard BJ; Chen Q; Blajchman MA; Ofosu FA; Sridhara S; Yang D; Clarke BJ
Blood; 1998 Jan; 91(1):142-8. PubMed ID: 9414278
[TBL] [Abstract][Full Text] [Related]
24. Factor VII Gene Defects: Review of Functional Studies and Their Clinical Implications.
Shahbazi S; Mahdian R
Iran Biomed J; 2019 May; 23(3):165-74. PubMed ID: 30797223
[TBL] [Abstract][Full Text] [Related]
25. Factor VII deficiency and the FVII mutation database.
McVey JH; Boswell E; Mumford AD; Kemball-Cook G; Tuddenham EG
Hum Mutat; 2001; 17(1):3-17. PubMed ID: 11139238
[TBL] [Abstract][Full Text] [Related]
26. [Haplotype Analysis of Coagulation Factor VII Gene in a Patient with Congenital Coagulation Factor VII Deficiency with Heterozygous p.Arg337Cys Mutation and o.Aro413Gin Polymorphism..].
Suzuki K; Yoshioka T; Obara T; Suwabe A
Rinsho Byori; 2016 May; 64(4):380-386. PubMed ID: 29182802
[TBL] [Abstract][Full Text] [Related]
27. Modular arrangement and secretion of a multidomain serine protease. Evidence for involvement of proline-rich region and N-glycans in the secretion pathway.
Wang J; Tan NS; Ho B; Ding JL
J Biol Chem; 2002 Sep; 277(39):36363-72. PubMed ID: 12089146
[TBL] [Abstract][Full Text] [Related]
28. Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity.
Peyvandi F; De Cristofaro R; Akhavan S; Carew JA; Landolfi R; Bauer KA; Mannucci PM
Thromb Haemost; 2002 Nov; 88(5):750-5. PubMed ID: 12428089
[TBL] [Abstract][Full Text] [Related]
29. Twenty two novel mutations of the factor VII gene in factor VII deficiency.
Wulff K; Herrmann FH
Hum Mutat; 2000; 15(6):489-96. PubMed ID: 10862079
[TBL] [Abstract][Full Text] [Related]
30. Human factor VII deficiency caused by S339C mutation located adjacent to the specificity pocket of the catalytic domain.
Takamiya O; Seta M; Tanaka K; Ishida F
Clin Lab Haematol; 2002 Aug; 24(4):233-8. PubMed ID: 12181027
[TBL] [Abstract][Full Text] [Related]
31. Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
Mota L; Shetty S; Idicula-Thomas S; Ghosh K
Clin Chim Acta; 2009 Nov; 409(1-2):106-11. PubMed ID: 19751712
[TBL] [Abstract][Full Text] [Related]
32. All post-translational modifications except propeptide cleavage are required for optimal secretion of coagulation factor VII.
Bolt G; Steenstrup TD; Kristensen C
Thromb Haemost; 2007 Nov; 98(5):988-97. PubMed ID: 18000603
[TBL] [Abstract][Full Text] [Related]
33. Identification of two novel mutations in three children with congenital factor VII deficiency.
Liang K; Nikuze L; Zhang F; Lu Z; Wei M; Wei H
Blood Coagul Fibrinolysis; 2021 Jul; 32(5):340-343. PubMed ID: 33587484
[TBL] [Abstract][Full Text] [Related]
34. More than one intracellular processing bottleneck delays the secretion of coagulation factor VII.
Bolt G; Kristensen C; Steenstrup TD
Thromb Haemost; 2008 Aug; 100(2):204-10. PubMed ID: 18690338
[TBL] [Abstract][Full Text] [Related]
35. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
Hu YN; Gan YM; Zhang YP; Ruan DD; Zhu YB; Lin XF; Fang ZT; Liao LS; Tang FQ; Luo JW
J Gene Med; 2022 Feb; 24(2):e3398. PubMed ID: 34786791
[TBL] [Abstract][Full Text] [Related]
36. Degradation of a short-lived glycoprotein from the lumen of the endoplasmic reticulum: the role of N-linked glycans and the unfolded protein response.
de Virgilio M; Kitzmüller C; Schwaiger E; Klein M; Kreibich G; Ivessa NE
Mol Biol Cell; 1999 Dec; 10(12):4059-73. PubMed ID: 10588643
[TBL] [Abstract][Full Text] [Related]
37. Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency.
Branchini A; Rizzotto L; Mariani G; Napolitano M; Lapecorella M; Giansily-Blaizot M; Mari R; Canella A; Pinotti M; Bernardi F
Haematologica; 2012 May; 97(5):705-9. PubMed ID: 22180436
[TBL] [Abstract][Full Text] [Related]
38. The role of N-glycan in folding, trafficking and pathogenicity of myelin oligodendrocyte glycoprotein (MOG).
Jung J; Dudek E; Michalak M
Biochim Biophys Acta; 2015 Sep; 1853(9):2115-21. PubMed ID: 25541284
[TBL] [Abstract][Full Text] [Related]
39. Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation.
Fromovich-Amit Y; Zivelin A; Rosenberg N; Landau M; Rosa JP; Seligsohn U
Blood Coagul Fibrinolysis; 2005 Jul; 16(5):369-74. PubMed ID: 15970722
[TBL] [Abstract][Full Text] [Related]
40. Lethal factor VII deficiency due to novel mutations in the F7 promoter: functional analysis reveals disruption of HNF4 binding site.
Giansily-Blaizot M; Lopez E; Viart V; Chafa O; Tapon-Bretaudière J; Claustres M; Taulan M
Thromb Haemost; 2012 Aug; 108(2):277-83. PubMed ID: 22628013
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]