4.7 Article

A missense mutation underlies defective SOCS4 function in a family with autoimmunity

Related references

Note: Only part of the references are listed.
Article Multidisciplinary Sciences

Genome sequencing identifies major causes of severe intellectual disability

Christian Gilissen et al.

NATURE (2014)

Article Genetics & Heredity

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

Sarah E. Flanagan et al.

NATURE GENETICS (2014)

Article Genetics & Heredity

Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes

Slave Petrovski et al.

PLOS GENETICS (2013)

Article Rheumatology

Targeting interleukin-17 in patients with active rheumatoid arthritis: rationale and clinical potential

Herbert Kellner

THERAPEUTIC ADVANCES IN MUSCULOSKELETAL DISEASE (2013)

Article Biochemistry & Molecular Biology

Defining a tissue stem cell-driven Runx1/Stat3 signalling axis in epithelial cancer

Cornelia Johanna Franziska Scheitz et al.

EMBO JOURNAL (2012)

Article Immunology

Sex differences and genomics in autoimmune diseases

Shashi Amur et al.

JOURNAL OF AUTOIMMUNITY (2012)

Article Biochemistry & Molecular Biology

Antiviral role of toll-like receptors and cytokines against the new 2009 H1N1 virus infection

Ye Liu et al.

MOLECULAR BIOLOGY REPORTS (2012)

Article Medicine, General & Internal

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

Joep de Ligt et al.

NEW ENGLAND JOURNAL OF MEDICINE (2012)

Article Medicine, General & Internal

STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis

Frank L. van de Veerdonk et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Article Genetics & Heredity

Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome

Christian Gilissen et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2010)

Review Immunology

IL-6: Regulator of Treg/Th17 balance

Akihiro Kimura et al.

EUROPEAN JOURNAL OF IMMUNOLOGY (2010)

Review Immunology

IL-6: from its discovery to clinical applications

Tadamitsu Kishimoto

INTERNATIONAL IMMUNOLOGY (2010)

Article Genetics & Heredity

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

Alexander Hoischen et al.

NATURE GENETICS (2010)

Article Multidisciplinary Sciences

Targeted capture and massively parallel sequencing of 12 human exomes

Sarah B. Ng et al.

NATURE (2009)

Article Multidisciplinary Sciences

Activation of EGFR on monocytes is required for human cytomegalovirus entry and mediates cellular motility

Gary Chan et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Article Public, Environmental & Occupational Health

Autoimmune diseases: A leading cause of death among young and middle-aged women in the United States

SJ Walsh et al.

AMERICAN JOURNAL OF PUBLIC HEALTH (2000)