Lista de obras - Arseni Markoff - Dominio Público Uruguay

Annexin A5 haplotype M2 is not a risk factor for recurrent spontaneous abortion in Northern Europe: is there sufficient evidence?

artículo científico publicado en 2016

Annexin A5 interacts with polycystin-1 and interferes with the polycystin-1 stimulated recruitment of E-cadherin into adherens junctions.

artículo científico publicado en 2007

Assessment of M2/ANXA5 haplotype as a risk factor in couples with placenta-mediated pregnancy complications

artículo científico publicado en 2017

Autosomal dominant polycystic kidney disease - clinical and genetic aspects

artículo científico publicado en 2002

Chromosomal evolution of the PKD1 gene family in primates

article

Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols

artículo científico publicado en 1998

Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population

artículo científico publicado en 2017

Hereditary thrombophilic risk factors for recurrent pregnancy loss.

artículo científico publicado en 2010

M2/ANXA5 haplotype as a predisposition factor in Malay women and couples experiencing recurrent spontaneous abortion: a pilot study

artículo científico publicado en 2015

Micromolar Zinc in Annexin A5 Anticoagulation as a Potential Remedy for RPRGL3-Associated Recurrent Pregnancy Loss

artículo científico publicado en 2018

Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families.

artículo científico publicado en 2002

Paternal and maternal carriage of the annexin A5 M2 haplotype are equal risk factors for recurrent pregnancy loss: a pilot study.

artículo científico publicado en 2012

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.

artículo científico publicado en 2002

Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations

artículo científico publicado en 2000

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

scientific article published on 01 January 2002

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.

artículo científico publicado en 2001

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A.

artículo científico publicado en 2007

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.

artículo científico publicado en 2005

Structural and functional characterisation of the mouse annexin A9 promoter.

artículo científico publicado en 2004

The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages

artículo científico publicado en 2017

Lista de obras de Arseni Markoff

Annexin A5 haplotype M2 is not a risk factor for recurrent spontaneous abortion in Northern Europe: is there sufficient evidence?

Annexin A5 interacts with polycystin-1 and interferes with the polycystin-1 stimulated recruitment of E-cadherin into adherens junctions.

Assessment of M2/ANXA5 haplotype as a risk factor in couples with placenta-mediated pregnancy complications

Autosomal dominant polycystic kidney disease - clinical and genetic aspects

Chromosomal evolution of the PKD1 gene family in primates

Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols

Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population

Hereditary thrombophilic risk factors for recurrent pregnancy loss.

M2/ANXA5 haplotype as a predisposition factor in Malay women and couples experiencing recurrent spontaneous abortion: a pilot study

Micromolar Zinc in Annexin A5 Anticoagulation as a Potential Remedy for RPRGL3-Associated Recurrent Pregnancy Loss

Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families.

Paternal and maternal carriage of the annexin A5 M2 haplotype are equal risk factors for recurrent pregnancy loss: a pilot study.

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.

Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A.

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.

Structural and functional characterisation of the mouse annexin A9 promoter.

The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages