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Eric P Hanson

Showing results (1-10 of 20) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|March 5, 2015
A method for the quantitative analysis of stimulation-induced nuclear translocation of the p65 subunit of NF-κB from patient-derived dermal fibroblastsAlex W Wessel, Eric P Hanson
Frontiers in Immunology|September 29, 2025
RIPK1 signaling pathways: implications for autoimmune and neuroinflammatory diseasesAbigail Pajulas, Jonathan T Sims, Eric P Hanson, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 28, 2011
Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levelsGital Karamchandani-Patel, Eric P Hanson, Rushani Saltzman, et al.
Frontiers in Pediatrics|May 2, 2015
Corrigendum: Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric SyndromeNicholas L Rider, Bertrand Boisson, Soma Jyonouchi, et al.
Frontiers in Pediatrics|February 18, 2015
Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric SyndromeNicholas L Rider, Bertrand Boisson, Soma Jyonouchi, et al.
The Journal of Allergy and Clinical Immunology|October 15, 2008
Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversityEric P Hanson, Linda Monaco-Shawver, Laura A Solt, et al.
Journal of Clinical Immunology|July 24, 2010
A novel missense mutation in the nuclear factor-κB essential modulator (NEMO) gene resulting in impaired activation of the NF-κB pathway and a unique clinical phenotype presenting as MRSA subdural empyemaGene A Devora, Lijun Sun, Zhijian Chen, et al.
The Journal of Allergy and Clinical Immunology|January 9, 2008
IKBKG (nuclear factor-kappa B essential modulator) mutation can be associated with opportunistic infection without impairing Toll-like receptor functionBryn H Salt, Julie E Niemela, Rahul Pandey, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 10, 2010
Cutting edge: association with I kappa B kinase beta regulates the subcellular localization of Homer3Gayatri Yatherajam, Pinaki P Banerjee, Kelly A McCorkell, et al.
Frontiers in Immunology|May 9, 2012
Hypohidrotic ectodermal dysplasia and immunodeficiency with coincident NEMO and EDA mutationsMichael D Keller, Maureen Petersen, Peck Ong, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|March 5, 2015
A method for the quantitative analysis of stimulation-induced nuclear translocation of the p65 subunit of NF-κB from patient-derived dermal fibroblastsAlex W Wessel, Eric P Hanson
Frontiers in Immunology|September 29, 2025
RIPK1 signaling pathways: implications for autoimmune and neuroinflammatory diseasesAbigail Pajulas, Jonathan T Sims, Eric P Hanson, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 28, 2011
Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levelsGital Karamchandani-Patel, Eric P Hanson, Rushani Saltzman, et al.
Frontiers in Pediatrics|May 2, 2015
Corrigendum: Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric SyndromeNicholas L Rider, Bertrand Boisson, Soma Jyonouchi, et al.
Frontiers in Pediatrics|February 18, 2015
Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric SyndromeNicholas L Rider, Bertrand Boisson, Soma Jyonouchi, et al.
The Journal of Allergy and Clinical Immunology|October 15, 2008
Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversityEric P Hanson, Linda Monaco-Shawver, Laura A Solt, et al.
Journal of Clinical Immunology|July 24, 2010
A novel missense mutation in the nuclear factor-κB essential modulator (NEMO) gene resulting in impaired activation of the NF-κB pathway and a unique clinical phenotype presenting as MRSA subdural empyemaGene A Devora, Lijun Sun, Zhijian Chen, et al.
The Journal of Allergy and Clinical Immunology|January 9, 2008
IKBKG (nuclear factor-kappa B essential modulator) mutation can be associated with opportunistic infection without impairing Toll-like receptor functionBryn H Salt, Julie E Niemela, Rahul Pandey, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 10, 2010
Cutting edge: association with I kappa B kinase beta regulates the subcellular localization of Homer3Gayatri Yatherajam, Pinaki P Banerjee, Kelly A McCorkell, et al.
Frontiers in Immunology|May 9, 2012
Hypohidrotic ectodermal dysplasia and immunodeficiency with coincident NEMO and EDA mutationsMichael D Keller, Maureen Petersen, Peck Ong, et al.
Pageof 2