4.6 Article

Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia

Related references

Note: Only part of the references are listed.
Review Genetics & Heredity

Diagnosis and treatment of inherited thrombocytopenias

A. Pecci

CLINICAL GENETICS (2016)

Review Hematology

Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias

Remi Favier et al.

BRITISH JOURNAL OF HAEMATOLOGY (2015)

Review Hematology

Lessons in platelet production from inherited thrombocytopenias

Alessandro Pecci et al.

BRITISH JOURNAL OF HAEMATOLOGY (2014)

Article Immunology

Distinct, strict requirements for Gfi-1b in adult bone marrow red cell and platelet generation

Adlen Foudi et al.

JOURNAL OF EXPERIMENTAL MEDICINE (2014)

Article Medicine, General & Internal

A Dominant-Negative GFI1B Mutation in the Gray Platelet Syndrome

Davide Monteferrario et al.

NEW ENGLAND JOURNAL OF MEDICINE (2014)

Article Multidisciplinary Sciences

Transcriptional diversity during lineage commitment of human blood progenitors

Lu Chen et al.

SCIENCE (2014)

Article Genetics & Heredity

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

Shinji Kunishima et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2013)

Article Hematology

GFI1B mutation causes a bleeding disorder with abnormal platelet function

W. S. Stevenson et al.

JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2013)

Article Hematology

Inherited platelet disorders

A. T. Nurden et al.

HAEMOPHILIA (2012)

Article Multidisciplinary Sciences

Frequent pathway mutations of splicing machinery in myelodysplasia

Kenichi Yoshida et al.

NATURE (2011)

Article Biochemistry & Molecular Biology

Direct transcriptional repression of the genes encoding the zinc-finger proteins Gfi1b and Gfi1 by Gfi1b

L Vassen et al.

NUCLEIC ACIDS RESEARCH (2005)

Article Genetics & Heredity

Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2

RE Person et al.

NATURE GENETICS (2003)