IKK-related genetic diseases: probing NF-κB functions in humans and other matters. - Wikidata - awgldk - TriplyDB

IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

http://www.wikidata.org/entity/Q38272499

about

BK virus encephalopathy and sclerosing vasculopathy in a patient with hypohidrotic ectodermal dysplasia and immunodeficiency Mutation of cysteine 46 in IKK-beta increases inflammatory responses.The BCR-ABL/NF-κB signal transduction network: a long lasting relationship in Philadelphia positive Leukemias Ikk2 regulates cytokinesis during vertebrate development.Succinamide derivatives of melampomagnolide B and their anti-cancer activities.Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemia.Interactome analysis of transforming growth factor-β-activated kinase 1 in Helicobacter pylori-infected cells revealed novel regulators tripartite motif 28 and CDC37.Pyrrolidine dithiocarbamate attenuates paraquat-induced acute pulmonary poisoning in vivo via transforming growth factor β1 and nuclear factor κB pathway interaction.NF-κB in Hematological Malignancies.The NF-κB Inhibitor, IMD-0354, Affects Immune Gene Expression, Bacterial Microbiota and Infection in Midgut

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IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

http://www.wikidata.org/entity/Q38272499

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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2014年论文

@zh-cn

name

IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

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type

label

IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

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prefLabel

IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

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Cellular and Molecular Life Sciences

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IKK-related genetic diseases: probing NF-κB functions in humans and other matters.

@en

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Alice Gentil Dit Maurin

http://www.w3.org/2001/XMLSchema#string

Anna Senegas

http://www.w3.org/2001/XMLSchema#string

Gilles Courtois

http://www.w3.org/2001/XMLSchema#string

Jérémie Gautheron

http://www.w3.org/2001/XMLSchema#string

P2860

Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus

TRAF6-deficient mice display hypohidrotic ectodermal dysplasia.

RIP4 (DIK/PKK), a novel member of the RIP kinase family, activates NF-kappa B and is processed during apoptosis.

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)

Beyond NF-κB activation: nuclear functions of IκB kinase α

Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity

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

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

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

Mutant CHUK and severe fetal encasement malformation

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s00018-014-1793-y

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1275-1287

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scholarly article

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10.1007/S00018-014-1793-Y

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7

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268974995

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25432706

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