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Publications by Jordan Pinder

Dominant Negative Gfi1b Mutations Cause Moderate Thrombocytopenia and an Impaired Stress Thrombopoiesis Associated With Mild Erythropoietic Abnormalities in Mice

Haematologica

Hematology

2019

English

Related publications

Dominant-Negative STAT5B Mutations Cause Growth Hormone Insensitivity With Short Stature and Mild Immune Dysregulation

Nature Communications

English

Combined Alpha-Delta Platelet Storage Pool Deficiency Is Associated With Mutations in GFI1B

Molecular Genetics and Metabolism

English

Erythrocyte Ankyrin Promoter Mutations Associated With Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression

Journal of Biological Chemistry

English

Mutations in SEC63 Cause Autosomal Dominant Polycystic Liver Disease

Nature Genetics

Genetics

2004

English

Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration

American Journal of Human Genetics

Genetics

2008

English

Fibrinolysis in Patients With a Mild-To-Moderate Bleeding Tendency of Unknown Cause

English

Chronic Mild Stress Modified Epigenetic Mechanisms Leading to Accelerated Senescence and Impaired Cognitive Performance in Mice

International Journal of Molecular Sciences

Organic Chemistry

Molecular Biology

Theoretical Chemistry

Inorganic Chemistry

Computer Science Applications

English

Lymphatic Abnormalities Are Associated With RASA1 Gene Mutations in Mouse and Man

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2013

English

Mice With Calr Mutations Homologous to Human CALR Mutations Only Exhibit Mild Thrombocytosis

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Jordan Pinder

Dominant Negative Gfi1b Mutations Cause Moderate Thrombocytopenia and an Impaired Stress Thrombopoiesis Associated With Mild Erythropoietic Abnormalities in Mice

Related publications

Dominant-Negative STAT5B Mutations Cause Growth Hormone Insensitivity With Short Stature and Mild Immune Dysregulation

Combined Alpha-Delta Platelet Storage Pool Deficiency Is Associated With Mutations in GFI1B

Erythrocyte Ankyrin Promoter Mutations Associated With Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression

Mutations in SEC63 Cause Autosomal Dominant Polycystic Liver Disease

Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration

Fibrinolysis in Patients With a Mild-To-Moderate Bleeding Tendency of Unknown Cause

Chronic Mild Stress Modified Epigenetic Mechanisms Leading to Accelerated Senescence and Impaired Cognitive Performance in Mice

Lymphatic Abnormalities Are Associated With RASA1 Gene Mutations in Mouse and Man

Mice With Calr Mutations Homologous to Human CALR Mutations Only Exhibit Mild Thrombocytosis