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Publications by Judith S. Greengard
Two Mutations in the Promoter Region of the Human Protein C Gene Both Cause Type I Protein C Deficiency by Disruption of Two HNF-3 Binding Sites
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Identification of Two Novel Mutations Associated With Combined Protein C and Protein S Deficiency
Vascular Diseases and Therapeutics
Functional Analysis of Two Haplotypes of the Human Endothelial Protein C Receptor Gene
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Protein C Deficiency: A Cause of Amaurosis Fugax?
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
No Effect of the Prothrombin G20210A Mutation on Protein C Activation in a Large Kindred With Type I Protein C Deficiency
Blood Coagulation and Fibrinolysis
Medicine
Hematology
Use of Human Protein C Concentrates in the Treatment of Patients With Severe Congenital Protein C Deficiency
Biologics: Targets and Therapy
Oncology
Immunology
Gastroenterology
Pharmacology
Rheumatology
Allergy
Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.
Journal of Medical Genetics
Genetics
Two Mechanisms of Ion Selectivity in Protein Binding Sites
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Identification of a C-Reactive Protein Binding Site in Two Hepatic Carboxylesterases Capable of Retaining C-Reactive Protein Within the Endoplasmic Reticulum
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Characterization of the C-Myb-Responsive Region and Regulation of the Human Type I Collagen Α2 Chain Gene by C-Myb
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
