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Articles (90)

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1-10 of 90 results for Factor X mutations

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Select article: A New Mutation (Arg251 Trp) in the Ca2+ Binding Site of Factor X Protease Domain Appears to be Responsible for the Defect in the Extrinsic Pathway Activation of Factor X Padua

Free access

Research article

First published 2004-01

A New Mutation (Arg251 Trp) in the Ca2+ Binding Site of Factor X Protease Domain Appears to be Responsible for the Defect in the Extrinsic Pathway Activation of Factor X Padua

Antonio Girolami, Fabrizio Vianello, Laura Cabrio [...]

Clinical and Applied Thrombosis/Hemostasis

Select article: Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4

Open access

Research article

First published 2023-10

Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4

R. Shemirani, M.H. Le, Y. Nakano

Journal of Dental Research

Select article: The rate of change of hereditary factors in Drosophila

Retricted access

Research article

First published 1919-10

The rate of change of hereditary factors in Drosophila

H. J. Muller, E. Altenburg

Experimental Biology and Medicine

Select article: A Unique Case of Renal Carcinoma with Xp11.2 Translocations/TFE3 Gene Fusions in a 3-Year-old Child,with Coexistent von Hippel-Lindau Gene Mutation

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Research article

First published 2004-7

A Unique Case of Renal Carcinoma with Xp11.2 Translocations/TFE3 Gene Fusions in a 3-Year-old Child,with Coexistent von Hippel-Lindau Gene Mutation

Mana M. Parast, Grant Eudy, Kenneth W. Gow [...]

Pediatric and Developmental Pathology

Select article: X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

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Other

First published 2008-01

X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

Xinhua Bao, Shengling Jiang, Fuying Song [...]

Journal of Child Neurology

Select article: A case report of congenital factor X deficiency in an adult patient

Open access

Case report

First published 2022

A case report of congenital factor X deficiency in an adult patient

Rehab Y AL-Ansari, Ghufran Alofi, Nasser Aljarah [...]

Sage Open Medical Case Reports

Select article: MECP2 and Beyond: Phenotype—Genotype Correlations in Rett Syndrome

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Other

First published 2003-10

MECP2 and Beyond: Phenotype—Genotype Correlations in Rett Syndrome

John Christodoulou, Linda S. Weaving

Journal of Child Neurology

Select article: The influence of lactic acid upon the metabolism of the dog. 1

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Research article

First published 1919-10

The influence of lactic acid upon the metabolism of the dog. 1

Graham Lusk, H. V. Atkinson

Experimental Biology and Medicine

Select article: Prevalence of Intron 1 Inversion of Cases With Hemophilia A in North Indian Population

Free access

Research article

First published 2012-11

Prevalence of Intron 1 Inversion of Cases With Hemophilia A in North Indian Population

Nuzhat Jahan Faridi, Praveen Kumar, Nuzhat Husain

Clinical and Applied Thrombosis/Hemostasis

Select article: Cleft Lip with Cleft Palate,Ankyloglossia,and Hypodontia are Associated with TBX22 Mutations

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Research article

First published 2011-4

Cleft Lip with Cleft Palate,Ankyloglossia,and Hypodontia are Associated with TBX22 Mutations

P.N. Kantaputra, M. Paramee, A. Kaewkhampa [...]

Journal of Dental Research

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