Showing 120 of 120on this page. Filters & sort apply to loaded results; URL updates for sharing.120 of 120 on this page
Identification of a missense mutation of NEMO causing a severe form of ...
The NEMO Mutation Creating the Most-Upstream Premature Stop Codon Is ...
Hypomorphic NEMO mutation database and reconstitution system identifies ...
Mutation of NEMO SUMOylation sites Lys-277 and Lys-309 attenuates ...
NEMO K270A mutation hampers autophagy. PLAT-E cells were transfected ...
TAB2-NZF-containing NEMO chimeras with UBAN mutation selectively binds ...
Pedigree of the NEMO gene mutation family. An X-linked dominant ...
NEMO X420W mutation results in impaired, but not abolished, NF-B ...
NEMO K270A mutation instigates systemic inflammation. Serum was ...
Correction of immunodeficiency associated with NEMO mutation by ...
Mechanism of colitis in NEMO hypomorphic mutations. NEMO, the ...
Genetic and in silico analysis of NEMO Protein. (A) and (B) show the ...
NEMO mutations in patients with HED-ID. A schematic diagram of the ...
A Review of NEMO Protein and its Relationship with Genetic Diseases
Specific Recognition of Linear Ubiquitin Chains by NEMO Is Important ...
In vitro functional analysis of NEMO variants. a NF-κB reporter gene ...
Overview of the functional domains of the NEMO protein. Genetic ...
NEMO mutations in the patients. A, Mutant (bottom) and wild-type (WT ...
Variably decreased WT NEMO protein caused by IKBKG intronic splice-site ...
Directed mutagenesis of NEMO selectively impairs binding to linear ...
Analysis of variant NEMO proteins containing disease-linked point ...
NEMO revertant T cells in patient 3. (A) Intracellular expression of ...
Schematic representation of NEMO and ΔNEMO pseudogene location in Xq28 ...
Analysis of NEMO protein expression using intracellular staining and ...
General structure of the 5' portion of the human NEMO gene. (A) Shown ...
(PDF) A Review of NEMO Protein and its Relationship with Genetic Diseases
Reduced NEMO expression was caused by duplication of the NEMO gene. (A ...
Analysis of NEMO protein expression and cytokine responses after UCBT ...
Expression of NEMO in the patients. NEMO protein, detected by Western ...
NEMO mutations found in human diseases. a Truncating mutations ...
Evaluation of nuclear NF-κB level in cells from a patient with NEMO ...
Functional analysis of NEMO ubiquitination. (A) Participation of NEMO ...
NEMO mutations. (a) Pedigrees of the two families with affected ...
Recruitment of A20 by the C-terminal domain of NEMO suppresses NF-κB ...
Clinical phenotypes and NEMO genotypes of patients. (A) Pedigrees of ...
The functional and structural domains of NEMO. A, the murine NEMO ...
Punnett's Square: Genetically programmed alternative splicing of NEMO ...
Phenotype of A323P mutation. (A) Defective response of A323P NEMO ...
Mutagenetix > Phenotypic Mutation
The IKK-binding domain of NEMO is an irregular coiled coil with a ...
NEMO zinc fi nger point mutations greatly compromise the ability of the ...
Pedigrees of the families with heterozygous NEMO mutations and clinical ...
JCI - Genetically programmed alternative splicing of NEMO mediates an ...
(PDF) Specific NEMO mutations impair CD40-mediated c-Rel activation and ...
NEMO Links Nuclear Factor-κB to Human Diseases: Trends in Molecular ...
Map demonstrating the NEMO hypomorphism (red) in the patient relative ...
Deficient NK cell cytotoxicity in patients with HED-ID and NEMO ...
DNA rearrangements of the NEMO and ψ-NEMO loci. In the upper part of ...
JCI - Specific NEMO mutations impair CD40-mediated c-Rel activation and ...
Deletion of Nemo in brain endothelial cells causes brain endothelial ...
Inactivation of the Nemo gene induces cell mitosis in cerebral vessels ...
Figure 4 from Identification of TRAF6-dependent NEMO polyubiquitination ...
Figure 2 from A Review of NEMO Protein and its Relationship with ...
A novel missense mutation in the nuclear factor-κB essential modulator ...
Specific NEMO mutations impair CD40-mediated c-Rel activation and B ...
JCI - Rescue of recurrent deep intronic mutation underlying cell type ...
Rescue of recurrent deep intronic mutation underlying cell type ...
Figure 2 from X-linked ectodermal dysplasia with immunodeficiency ...
Home [www.winklhoferlab.ruhr-uni-bochum.de]
Genetic and Inheritance
The NEMO/IKBKG locus. (a) Schematic representation of the genomic ...
Domain structure of NEMO. (A) Schematic representation of the structure ...
JCI - Deficient natural killer cell cytotoxicity in patients with IKK-γ ...
NEMO-Ub binding is essential for TNFα signaling, but not for IL-1β ...
Skin phenotype of mice with epidermis-specific deletion of NEMO. ( A ...
(A) NEMO-null cells expressing IκBαSR were transduced with retrovirus ...
Disseminated BCG Infectious Disease and Hyperferritinemia in a Patient ...
Frontiers | Hypohidrotic ectodermal dysplasia and immunodeficiency with ...
Two-sided Ubiquitin Binding of NF-κB Essential Modulator (NEMO) Zinc ...
CRISPR/Cas9-based editing of a sensitive transcriptional regulatory ...
Figure 1 from The Common NF-κB Essential Modulator (NEMO) Gene ...
Case 10 - Clinical GateClinical Gate
Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex ...
Clinical relevance of loss-of-function mutations of NEMO/IKBKG - PMC
A male infant with anhidrotic ectodermal dysplasia/immunodeficiency ...
Figure 1 from X-linked ectodermal dysplasia with immunodeficiency ...
.gif)
.gif)
