Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways (Q35091428)

6 August 2017

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title

Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways (English)

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6 August 2017

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Rieux-Laucat F

1

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6 August 2017

Le Deist F

series ordinal

2

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6 August 2017

Fischer A

series ordinal

3

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6 August 2017

publication date

1 January 2003

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Cell Death & Differentiation

6 August 2017

published in

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6 August 2017

volume

10

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6 August 2017

issue

1

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6 August 2017

page(s)

124-133

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Death receptors: signaling and modulation

6 August 2017

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Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II

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The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosis

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7 January 2021

Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance

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7 January 2021

The molecular basis for apoptotic defects in patients with CD95 (Fas/Apo-1) mutations

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7 January 2021

Fas/Apo1 mutations and autoimmune lymphoproliferative syndrome in a patient with type 2 autoimmune hepatitis

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7 January 2021

An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndrome

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The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis

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Increases in circulating and lymphoid tissue interleukin-10 in autoimmune lymphoproliferative syndrome are associated with disease expression

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Pathological findings in human autoimmune lymphoproliferative syndrome

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7 January 2021

Identification of new Fas mutations in a patient with autoimmune lymphoproliferative syndrome (ALPS) and eosinophilia.

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7 January 2021

Autoimmune lymphoproliferative syndrome: a syndrome associated with inherited genetic defects that impair lymphocytic apoptosis--CT and US features

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7 January 2021

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7 January 2021

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Response to steroid therapy in autism secondary to autoimmune lymphoproliferative syndrome

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7 January 2021

Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

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7 January 2021

Fas-mediated apoptosis and activation-induced T-cell proliferation are defective in mice lacking FADD/Mort1

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7 January 2021

Enhanced CD4+ T cell proliferation and Th2 cytokine production in DR6-deficient mice

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7 January 2021

Impaired c-Jun amino terminal kinase activity and T cell differentiation in death receptor 6-deficient mice

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7 January 2021

DR3 regulates negative selection during thymocyte development

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7 January 2021

CD95 (Fas)-dependent elimination of self-reactive B cells upon interaction with CD4+T cells

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7 January 2021

The fas antigen is involved in peripheral but not thymic deletion of T lymphocytes in T cell receptor transgenic mice

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7 January 2021

Loci predisposing to autoimmunity in MRL-Fas lpr and C57BL/6-Faslpr mice

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7 January 2021

Identifiers

DOI

10.1038/SJ.CDD.4401190

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6 August 2017

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