4.7 Article

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome

Related references

Note: Only part of the references are listed.
Article Immunology

The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency

Venetia Bigley et al.

JOURNAL OF EXPERIMENTAL MEDICINE (2011)

Article Medicine, General & Internal

IRF8 Mutations and Human Dendritic-Cell Immunodeficiency

Sophie Hambleton et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Review Biochemistry & Molecular Biology

GATA Switches as Developmental Drivers

Emery H. Bresnick et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Letter Biochemical Research Methods

A method and server for predicting damaging missense mutations

Ivan A. Adzhubei et al.

NATURE METHODS (2010)

Article Multidisciplinary Sciences

Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia

Su-Jiang Zhang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Review Immunology

Defects in the interferon-γ and interleukin-12 pathways

SD Rosenzweig et al.

IMMUNOLOGICAL REVIEWS (2005)

Article Medicine, General & Internal

Clinical features of dominant and recessive interferon γ receptor 1 deficiencies

SE Dorman et al.

LANCET (2004)

Article Medicine, General & Internal

Brief report - Mutation of CEBPA in familial acute myeloid leukemia

ML Smith et al.

NEW ENGLAND JOURNAL OF MEDICINE (2004)