Finding NEMO: genetic disorders of NF-[kappa]B activation. - Wikidata - awgldk - TriplyDB

Finding NEMO: genetic disorders of NF-[kappa]B activation.

Finding NEMO: genetic disorders of NF-[kappa]B activation.

http://www.wikidata.org/entity/Q39912726

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Sepsis-induced Cardiac Mitochondrial Damage and Potential Therapeutic Interventions in the Elderly Inflammatory bowel disease in pediatric and adolescent patients: a biomolecular and histopathological review Cell penetrating peptide inhibitors of nuclear factor-kappa B.NF-κB Essential Modulator Deficiency Leading to Disseminated Cutaneous Atypical Mycobacteria.Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα.Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation.The hyper IgM syndrome--an evolving story.Mitochondrial ROS Induces Cardiac Inflammation via a Pathway through mtDNA Damage in a Pneumonia-Related Sepsis Model.Genetic susceptibility to mycobacterial disease in humans.Noncanonical NF-κB signaling is limited by classical NF-κB activity.TLR4 polymorphisms and disease susceptibility.Association of TLR1, TLR2, TLR4, TLR6, and TIRAP polymorphisms with disease susceptibility.Estrogen-provided cardiac protection following burn trauma is mediated through a reduction in mitochondria-derived DAMPs.Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanisms.

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Finding NEMO: genetic disorders of NF-[kappa]B activation.

http://www.wikidata.org/entity/Q39912726

description

2003 nî lūn-bûn

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2003年の論文

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2003年学术文章

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2003年学术文章

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2003年学术文章

@zh-hans

2003年学术文章

@zh-my

2003年学术文章

@zh-sg

2003年學術文章

@yue

2003年學術文章

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2003年學術文章

@zh-hant

name

Finding NEMO: genetic disorders of NF-[kappa]B activation.

@en

Finding NEMO: genetic disorders of NF-[kappa]B activation.

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type

label

Finding NEMO: genetic disorders of NF-[kappa]B activation.

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Finding NEMO: genetic disorders of NF-[kappa]B activation.

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prefLabel

Finding NEMO: genetic disorders of NF-[kappa]B activation.

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Finding NEMO: genetic disorders of NF-[kappa]B activation.

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Journal of Clinical Investigation

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Finding NEMO: genetic disorders of NF-[kappa]B activation.

@en

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Jordan S Orange

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Raif S Geha

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P2860

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Identification of the familial cylindromatosis tumour-suppressor gene

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium

Pyogenic bacterial infections in humans with IRAK-4 deficiency

CYLD is a deubiquitinating enzyme that negatively regulates NF-kappaB activation by TNFR family members

Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-kappaB

The tumour suppressor CYLD negatively regulates NF-kappaB signalling by deubiquitination

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983-985

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10.1172/JCI19960

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7

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112

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2003-10-01T00:00:00Z

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14523034

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200971

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