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Tumor suppressor CYLD: negative regulation of NF-kappaB signaling and more

Cellular and molecular life sciences : CMLS, 2008-04, Vol.65 (7-8), p.1123-1132

Courtois, G

2008

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Effect of annealing on silicon heterojunction solar cells with textured ZnO:Al as transparent conductive oxide

EPJ Photovoltaics, 2012-01, Vol.3, p.35002

2012

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Purified Hepatocyte Nuclear Factor 1 Interacts with a Family of Hepatocyte-Specific Promoters

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.7937-7941

1988

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NF-κB-related genetic diseases

Cell death and differentiation, 2006-05, Vol.13 (5), p.843-851

2006

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Spectrum of Manifolds with Holes

Journal of functional analysis, 1995, Vol.134 (1), p.194-221

Courtois, G.

1995

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EKLF-driven PIT1 expression is critical for mouse erythroid maturation in vivo and in vitro

Blood, 2013-01, Vol.121 (4), p.666-678

2013

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Caspase activated Rock-1 allows erythroblasts terminal maturation independently of cytokine induced Rho signaling

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2010-09, Vol.17 (3), p.201-201

Courtois, G.

2010

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HSP27 controls GATA-1 protein level during erythroid cell differentiation

Blood, 2010-07, Vol.116 (1), p.85-96

2010

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Down-regulating constitutive activation of the NF-κB canonical pathway overcomes the resistance of cutaneous T-cell lymphoma to apoptosis

Blood, 2006-03, Vol.107 (6), p.2354-2363

2006

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Pertinence de l’examen clinique en urgence pour le diagnostic des ruptures des faisceaux antérieur et moyen du ligament collatéral latéral de la cheville

Journal de traumatologie du sport, 2020-06, Vol.37 (2), p.80-87

2020

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TNF-mediated inflammatory skin disease in mice with epidermis-specific deletion of IKK2

Nature (London), 2002-06, Vol.417 (6891), p.861-866

2002

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CYLD (cylindromatosis (turban tumor syndrome))

Atlas of genetics and cytogenetics in oncology and haematology, 2011-11 (2)

Courtois, G

2011

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Human erythroleukemia: is the two-hit model of mouse leukemogenesis valid in human disease?

Leukemia, 2007-10, Vol.21 (10), p.2212-2214

2007

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Mature T Cells Depend on Signaling through the IKK Complex

Immunity (Cambridge, Mass.), 2003-09, Vol.19 (3), p.377-389

2003

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The NF-[kappa]B signaling pathway in human genetic diseases

Cellular and molecular life sciences : CMLS, 2005-08, Vol.62 (15), p.1682

Courtois, G

2005

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NEMO/IKKγ-Deficient Mice Model Incontinentia Pigmenti

Molecular cell, 2000-06, Vol.5 (6), p.981-992

2000

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Tax induces nuclear translocation of NF-kappa B through dissociation of cytoplasmic complexes containing p105 or p100 but does not induce degradation of I kappa B alpha/MAD3

Journal of Virology, 1994-12, Vol.68 (12), p.8035-8044

1994

Volltextzugriff (PDF)

Complementation Cloning of NEMO, a Component of the IκB Kinase Complex Essential for NF-κB Activation

Cell, 1998-06, Vol.93 (7), p.1231-1240

1998

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Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-κB activation

Human molecular genetics, 2004-08, Vol.13 (16), p.1763-1773

2004

Volltextzugriff (PDF)

A hypermorphic I Kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

The Journal of clinical investigation, 2003-10, Vol.112 (7), p.1108-1115

2003

Volltextzugriff (PDF)

A variant nuclear protein in dedifferentiated hepatoma cells binds to the same functional sequences in the beta fibrinogen gene promoter as HNF‐1

The EMBO journal, 1988-08, Vol.7 (8), p.2485-2493

1988

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Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti

Nature (London), 2000-05, Vol.405 (6785), p.466-472

2000

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NF-kappaB-related genetic diseases

Cell death and differentiation, 2006-05, Vol.13 (5), p.843-851

2006

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Tumor suppressor CYLD: negative regulation of NF-kappaB signaling and more

Effect of annealing on silicon heterojunction solar cells with textured ZnO:Al as transparent conductive oxide

Purified Hepatocyte Nuclear Factor 1 Interacts with a Family of Hepatocyte-Specific Promoters

NF-κB-related genetic diseases

Spectrum of Manifolds with Holes

EKLF-driven PIT1 expression is critical for mouse erythroid maturation in vivo and in vitro

Caspase activated Rock-1 allows erythroblasts terminal maturation independently of cytokine induced Rho signaling

HSP27 controls GATA-1 protein level during erythroid cell differentiation

Defective nuclear localization of Hsp70 is associated with dyserythropoiesis and GATA-1 cleavage in myelodysplastic syndromes

Down-regulating constitutive activation of the NF-κB canonical pathway overcomes the resistance of cutaneous T-cell lymphoma to apoptosis

Pertinence de l’examen clinique en urgence pour le diagnostic des ruptures des faisceaux antérieur et moyen du ligament collatéral latéral de la cheville

TNF-mediated inflammatory skin disease in mice with epidermis-specific deletion of IKK2

CYLD (cylindromatosis (turban tumor syndrome))

Human erythroleukemia: is the two-hit model of mouse leukemogenesis valid in human disease?

Mature T Cells Depend on Signaling through the IKK Complex

The NF-[kappa]B signaling pathway in human genetic diseases

NEMO/IKKγ-Deficient Mice Model Incontinentia Pigmenti

Tax induces nuclear translocation of NF-kappa B through dissociation of cytoplasmic complexes containing p105 or p100 but does not induce degradation of I kappa B alpha/MAD3

Complementation Cloning of NEMO, a Component of the IκB Kinase Complex Essential for NF-κB Activation

Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-κB activation

A hypermorphic I Kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling

A variant nuclear protein in dedifferentiated hepatoma cells binds to the same functional sequences in the beta fibrinogen gene promoter as HNF‐1

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti

NF-kappaB-related genetic diseases

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