Gene of the issue: GP1BA gene mutations associated with bleeding-Reference-Cited by-同舟云学术

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Gene of the issue: GP1BA gene mutations associated with bleeding

Published:2017-09-29 Issue:8 Volume:28 Page:832-836
ISSN:0953-7104
Container-title:Platelets
language:en
Short-container-title:Platelets

Author:

Othman Maha¹²,Emsley Jonas³

Affiliation:

1. Department of Biomedical and Molecular Sciences, Faculty of Medicine, Queen’s University, Kingston, Canada

2. School of Baccalaureate Nursing, St. Lawrence College, Kingston, Canada

3. School of Pharmacy, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK

Publisher

Informa UK Limited

Subject

Hematology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/09537104.2017.1361526

Reference70 articles.

1. Glycoprotein Ibα forms disulfide bonds with 2 glycoprotein Ibβ subunits in the resting platelet

2. Bernard-Soulier syndrome (Hemorrhagiparous thrombocytic dystrophy)

3. Bernard-Soulier syndrome

4. Platelet glycoproteins and their role in diseases

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2. A method based on plateletpheresis to obtain functional platelet, CD3 ⁺ and CD14 ⁺ matched populations for research immunological studies;Clinical & Experimental Allergy;2022-07-16

3. Congenital and acquired disorders of primary hemostasis;Annals of Blood;2022-03

4. Thrombocytopathies: Not Just Aggregation Defects—The Clinical Relevance of Procoagulant Platelets;Journal of Clinical Medicine;2021-02-24

5. A novel mutation in GP1BA gene in a family with autosomal dominant Bernard Soulier syndrome variant: A case report;Experimental and Therapeutic Medicine;2021-02-13

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