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Publications by S R Russell

Expression of the Phenotypic Abnormality of Platelet-Type Von Willebrand Disease in a Recombinant Glycoprotein Ib Alpha Fragment.

Journal of Clinical Investigation

Medicine

1993

English

Vitreous and Retinal Amino Acid Concentrations in Experimental Central Retinal Artery Occlusion in the Primate

English

Related publications

Molecular Basis of Von Willebrand Disease Type IIB. Candidate Mutations Cluster in One Disulfide Loop Between Proposed Platelet Glycoprotein Ib Binding Sequences.

Journal of Clinical Investigation

Medicine

1991

English

Platelet Interaction With Von Willebrand Factor Is Enhanced by Shear-Induced Clustering of Glycoprotein Ib

Haematologica

Hematology

2013

English

Identification of Amino Acid Residues Essential for Von Willebrand Factor Binding to Platelet Glycoprotein Ib.

Journal of Biological Chemistry

English

Crystal Structure of the Von Willebrand Factor A1 Domain and Implications for the Binding of Platelet Glycoprotein Ib

Journal of Biological Chemistry

English

Von Willebrand Factor but Not -Thrombin Binding to Platelet Glycoprotein Ib Is Influenced by the HPA-2 Polymorphism

Arteriosclerosis, Thrombosis, and Vascular Biology

Cardiovascular Medicine

Cardiology

2003

English

Von Willebrand Disease Type 3

2020

English

Cloning of the Alpha Chain of Human Platelet Glycoprotein Ib: A Transmembrane Protein With Homology to Leucine-Rich Alpha 2-Glycoprotein.

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

Multidisciplinary

1987

English

Heterogeneous Phenotypes of Platelet and Plasma Von Willebrand Factor in Obligatory Heterozygotes for Severe Von Willebrand Disease

English

Variant Bernard-Soulier Syndrome Type Bolzano. A Congenital Bleeding Disorder Due to a Structural and Functional Abnormality of the Platelet Glycoprotein Ib-Ix Complex.

Journal of Clinical Investigation

Medicine

1990

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S R Russell

Expression of the Phenotypic Abnormality of Platelet-Type Von Willebrand Disease in a Recombinant Glycoprotein Ib Alpha Fragment.

Vitreous and Retinal Amino Acid Concentrations in Experimental Central Retinal Artery Occlusion in the Primate

Related publications

Molecular Basis of Von Willebrand Disease Type IIB. Candidate Mutations Cluster in One Disulfide Loop Between Proposed Platelet Glycoprotein Ib Binding Sequences.

Platelet Interaction With Von Willebrand Factor Is Enhanced by Shear-Induced Clustering of Glycoprotein Ib

Identification of Amino Acid Residues Essential for Von Willebrand Factor Binding to Platelet Glycoprotein Ib.

Crystal Structure of the Von Willebrand Factor A1 Domain and Implications for the Binding of Platelet Glycoprotein Ib

Von Willebrand Factor but Not -Thrombin Binding to Platelet Glycoprotein Ib Is Influenced by the HPA-2 Polymorphism

Von Willebrand Disease Type 3

Cloning of the Alpha Chain of Human Platelet Glycoprotein Ib: A Transmembrane Protein With Homology to Leucine-Rich Alpha 2-Glycoprotein.

Heterogeneous Phenotypes of Platelet and Plasma Von Willebrand Factor in Obligatory Heterozygotes for Severe Von Willebrand Disease

Variant Bernard-Soulier Syndrome Type Bolzano. A Congenital Bleeding Disorder Due to a Structural and Functional Abnormality of the Platelet Glycoprotein Ib-Ix Complex.