Add to ORKGBiallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunit
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...
BACKGROUND: The genetic cause of primary immunodeficiency disease (PID) carries prognostic informati...
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...
Primary immunodeficiency disorders enable identification of genes with crucial roles in the human im...
• A nonsense mutation in IKBKB caused the absence of IKKb and a lack of T- and B-cell activation thr...
Contains fulltext : 70805.pdf (publisher's version ) (Closed access)More than 11 g...
Primary immunodeficiency disorders (PIDs) render patients vulnerable to infection with a wide range ...
Primary immune deficiency diseases arise due to heritable defects that often involve signaling molec...
CITATION: Schlechter, N. et al. 2017. Exome sequencing identifies a novel MAP3K14 mutation in recess...
Inhibitor of nuclear factor kappa B kinase alpha (IKKα) is critical for p100/NF-κB2 phosphorylation ...
Hypomorphic IKBKG mutations in males are typically associated with anhidrotic ectodermal dysplasia w...
Loss of function mutations in the recombination activating genes RAG1 and RAG2 have been reported to...
Contains fulltext : 59285.pdf (publisher's version ) (Open Access)Both innate and ...
Background: The genetic etiology of primary immunodeficiency disease (PID) carries prognostic inform...
Background: The nuclear factor kappa light-chain enhancer of activated B cells (NF-kappa B) signalin...
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...
BACKGROUND: The genetic cause of primary immunodeficiency disease (PID) carries prognostic informati...
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...
Primary immunodeficiency disorders enable identification of genes with crucial roles in the human im...
• A nonsense mutation in IKBKB caused the absence of IKKb and a lack of T- and B-cell activation thr...
Contains fulltext : 70805.pdf (publisher's version ) (Closed access)More than 11 g...
Primary immunodeficiency disorders (PIDs) render patients vulnerable to infection with a wide range ...
Primary immune deficiency diseases arise due to heritable defects that often involve signaling molec...
CITATION: Schlechter, N. et al. 2017. Exome sequencing identifies a novel MAP3K14 mutation in recess...
Inhibitor of nuclear factor kappa B kinase alpha (IKKα) is critical for p100/NF-κB2 phosphorylation ...
Hypomorphic IKBKG mutations in males are typically associated with anhidrotic ectodermal dysplasia w...
Loss of function mutations in the recombination activating genes RAG1 and RAG2 have been reported to...
Contains fulltext : 59285.pdf (publisher's version ) (Open Access)Both innate and ...
Background: The genetic etiology of primary immunodeficiency disease (PID) carries prognostic inform...
Background: The nuclear factor kappa light-chain enhancer of activated B cells (NF-kappa B) signalin...
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...
BACKGROUND: The genetic cause of primary immunodeficiency disease (PID) carries prognostic informati...
NF-κB signaling, acting through NFKB1 dependent canonical and NFKB2 dependent non-canonical pathways...