Skip to search formSkip to main contentSkip to account menu

Protein C gene

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Childhood asthma is associated with polymorphic markers of PROC on 2q14 in addition to 17q21 locus
Childhood asthma is caused by both genetic and environmental factors. The first genomewide association study (GWAS) for asthma… 
2015
2015
Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay.
2014
2014
A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period
Homozygous protein C deficiency is among rare causes of thrombophilia. Herein, we present a neonate with purpura fulminans… 
2014
2014
The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency
Both compound heterozygous and homozygous protein C deficiencies (PCDs) can cause lethal thrombotic events in children. This… 
2013
2013
Budd-Chiari Syndrome with Multiple Thrombi due to a Familial Arg42Ser Mutation in the Protein C Gene
A 34-year-old Japanese woman was admitted to our hospital complaining of developing bilateral pedal edema. Imaging studies led to… 
2011
2011
Congenital factor XIII deficiency: A commentary on ‘Homozygous intronic mutation leading to inefficient transcription combined with a novel frame-shift mutation in F13A1 gene causes FXIII deficiency’
Congenital factor XIII deficiency: A commentary on ‘Homozygous intronic mutation leading to inefficient transcription combined… 
2009
2009
Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations
Protein C is a vitamin K-dependent plasma glycoprotein that functions as an important regulator of blood coagulation, and its… 
2001
2001
Sensitivity and specificity of denaturing high-pressure liquid chromatography for unknown protein C gene mutations.
Screening methods for unknown DNA sequence variations are laborious, expensive, and relatively insensitive. To evaluate the… 
1996
1996
Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G→A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency
We report the results of protein C gene (PROC) analysis in a Spanish family with hereditary PC deficiency characterized by the… 
1988
1988
Assignment of the human protein C gene (PROC) to chromosome region 2q14----q21 by in situ hybridization.
The protein C gene (PROC) was mapped by in situ hybridization. A genomic DNA probe containing the first three exons was 3H… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)