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PROC;jsessionid=9365A2F566CAB6412C90067ADE71CCCC
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Liver
Dendritic (plasmacytoid) cell
Fetal liver
Natural killer cell of peripheral blood
Macrophage of peripheral blood
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Most Correlated Diseases
Thrombophilia
Thrombosis
Blood coagulation disorder
Antiphospholipid syndrome
Infection by Schistosoma
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Most Correlated Compounds
Sodium Tetradecyl Sulfate
Taxol
Recombinant Fusion Proteins
1-hydroxycholecalciferol
Nortriptyline
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Most Correlated Gene Perturbations
MIR340
UPF2
COG2
ACTN4
BLM
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Literature
Most Relevant Literature
Performance of Chromogenic Protein C (PC) Testing.
The protein C pathways.
Analysis of the molecular pathogenesis of hereditary protein C deficiency due to a p.Gly86Asp varian…
Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in…
Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent fa…
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There were no clinical trials for PROC;jsessionid=9365A2F566CAB6412C90067ADE71CCCC
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