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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

376 related articles for article (PubMed ID: 15907525)

  • 41. Use of thromboelastography and thrombin generation assay to predict clinical phenotype in patients with severe FVII deficiency.
    Tran HT; Tjønnfjord GE; Holme PA
    Haemophilia; 2014 Jan; 20(1):141-6. PubMed ID: 23992369
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
    Takamiya O; Kemball-Cook G; Martin DM; Cooper DN; von Felten A; Meili E; Hann I; Prangnell DR; Lumley H; Tuddenham EG
    Hum Mol Genet; 1993 Sep; 2(9):1355-9. PubMed ID: 8242057
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation.
    Zhidong W; Xiaojun H
    Thromb Haemost; 2007 Sep; 98(3):687-8. PubMed ID: 17849063
    [No Abstract]   [Full Text] [Related]  

  • 44. [Double heterozygous mutations of non-canonical splice (IVS1a + 5g > a) and His348Gln caused inherited coagulation factor VII deficiency].
    Ding QL; Wang HL; Wang XF; Wang MS; Fu QH; Wu WM; Hu YQ; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2004 Mar; 25(3):139-42. PubMed ID: 15182580
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency.
    Branchini A; Ferrarese M; Lombardi S; Mari R; Bernardi F; Pinotti M
    J Thromb Haemost; 2016 Oct; 14(10):1994-2000. PubMed ID: 27513915
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Significant decrease in factor VII activity by tissue thromboplastin derived from rabbit brain in a patient with congenital factor VII deficiency (FVII Padua)].
    Sekiya A; Morishita E; Maruyama K; Asakura H; Nakao S; Ohtake S
    Rinsho Ketsueki; 2012 Mar; 53(3):357-60. PubMed ID: 22499055
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
    Millar DS; Kemball-Cook G; McVey JH; Tuddenham EG; Mumford AD; Attock GB; Reverter JC; Lanir N; Parapia LA; Reynaud J; Meili E; von Felton A; Martinowitz U; Prangnell DR; Krawczak M; Cooper DN
    Hum Genet; 2000 Oct; 107(4):327-42. PubMed ID: 11129332
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion.
    Hewitt J; Ballard JN; Nelson TN; Smith VC; Griffiths TA; Pritchard S; Wu JK; Wadsworth LD; Casey B; MacGillivray RT
    Br J Haematol; 2005 Feb; 128(3):380-5. PubMed ID: 15667541
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Similarities and discrepancies in homozygous factor VII defects due to mutations in the region of residues Met298 to Cys310 (exon 8) in the catalytic domain of factor VII.
    Girolami A; Berti de Marinis G; Bonamigo E; Vettore S
    Lab Hematol; 2011 Jun; 17(2):17-21. PubMed ID: 21705315
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation.
    Landau D; Rosenberg N; Zivelin A; Staretz-Chacham O; Kapelushnik J
    Haemophilia; 2009 May; 15(3):774-8. PubMed ID: 19432927
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Arg 304 Gln (FVII Padua) and Ala 294 Val mutations are equally present in patients with FVII deficiency and thrombosis.
    Girolami A; Candeo N; Bonamigo E; Fabris F
    Eur J Haematol; 2011 Jul; 87(1):92-4. PubMed ID: 21453389
    [No Abstract]   [Full Text] [Related]  

  • 52. Factor VII deficiency due to compound heterozygosity for Leu-48Pro mutation and a novel Pro260Leu mutation.
    Kogiso N; Taki M; Takamiya O
    Clin Appl Thromb Hemost; 2011; 17(6):E205-10. PubMed ID: 21441234
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations c.572-1G>A and c.1037A>C in a Chinese pedigree.
    Wei L; Fan C; Sun X; Wang X; Yu H
    Gene; 2024 Nov; 928():148788. PubMed ID: 39047958
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.
    Tamary H; Fromovich Y; Shalmon L; Reich Z; Dym O; Lanir N; Brenner B; Paz M; Luder AS; Blau O; Korostishevsky M; Zaizov R; Seligsohn U
    Thromb Haemost; 1996 Sep; 76(3):283-91. PubMed ID: 8883260
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [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]  

  • 56. Compound heterozygous mutations (p.Leu13Pro and p.Tyr294*) associated with factor VII deficiency cause impaired secretion through ineffective translocation and extensive intracellular degradation of factor VII.
    Suzuki K; Sugawara T; Ishida Y; Suwabe A
    Thromb Res; 2013 Feb; 131(2):166-72. PubMed ID: 23141848
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [An inherited coagulation factor VII deficiency pedigree caused by homozygous mutation of His348Gln].
    Jin YH; Wang MS; Niu ZZ; Xie YS; Xie HX; Yang LH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):10-3. PubMed ID: 21287501
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.
    Akhavan S; Mannucci PM; Lak M; Mancuso G; Mazzucconi MG; Rocino A; Jenkins PV; Perkins SJ
    Thromb Haemost; 2000 Dec; 84(6):989-97. PubMed ID: 11154146
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Four loops of the catalytic domain of factor viia mediate the effect of the first EGF-like domain substitution on factor viia catalytic activity.
    Jin J; Perera L; Stafford D; Pedersen L
    J Mol Biol; 2001 Apr; 307(5):1503-17. PubMed ID: 11292356
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp].
    Ding QL; Wang HL; Wang XF; Wang MS; Fu QH; Wu WM; Hu YQ; Wang ZY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):279-83. PubMed ID: 12903033
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.