Identification of a Severe Bleeding Disorder in Humans Caused by a Mutation in CalDAG-GEFI

Journal of Experimental Medicine - United States
doi 10.1084/jem.2117insight1
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Rockefeller University Press

Related search

Megakaryocytes Derived From Embryonic Stem Cells Implicate CalDAG-GEFI in Integrin Signaling

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2002English

Phosphorylation of the Guanine-Nucleotide-Exchange Factor CalDAG-GEFI by Protein Kinase a Regulates Ca2+-Dependent Activation of Platelet Rap1b GTPase

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
2013English

A CalDAG-GEFI/Rap1/B-Raf Cassette Couples M1Muscarinic Acetylcholine Receptors to the Activation of ERK1/2

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2001English

Identification of a Novel Mutation in the Factor VIII Gene Causing Severe Haemophilia A

BMC Hematology
HematologyMolecular Biology
2018English

Gastrointestinal Bleeding Caused by a Penetrating Aortic Ulcer

Clinical Gastroenterology and Hepatology
HepatologyGastroenterology
2017English

Recurrent Inflammatory Disease Caused by a Heterozygous Mutation in CD48

Journal of Allergy and Clinical Immunology
AllergyImmunology
2019English

Septal Myectomy for Severe Neonatal Hypertrophic Cardiomyopathy Caused by PTPN11 Gene Mutation: A Case Report

Biomedical Journal of Scientific & Technical Research
2019English

Fibrinogen as a Replacement Therapy in Bleeding Disorder

Egyptian Journal of Hematology and Bone Marrow Transplantation
2015English

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Annals of Otology, Rhinology and Laryngology
MedicineOtorhinolaryngology
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy