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Clinical Immunology (Orlando, Fla.)
|
March 13, 2019
Rethinking newborn screening for severe combined immunodeficiency: Lessons from an international partnership for patients with primary immunodeficiencies in Pakistan
Jacqueline G Wallace, Hamid Nawaz Tipu, Kelsey Stafstrom, et al.
Frontiers in Immunology
|
April 14, 2022
Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7Rα Chain
Rana Mansour, Yasmin El Bsat, Anthony Fadel, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 15, 2015
The Rho GTPase Cdc42 Is Essential for the Activation and Function of Mature B Cells
Natalija Gerasimcik, Carin I M Dahlberg, Marisa A P Baptista, et al.
Frontiers in Immunology
|
February 6, 2025
Deciphering the role of IL17RA in psoriasis and chronic mucocutaneous candidiasis: shared pathways and distinct manifestations
Ayat Kadhi, Edward Eid, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology
|
March 8, 2011
A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding
Michel J Massaad, Narayanaswamy Ramesh, Severine Le Bras, et al.
Cell Reports
|
July 19, 2018
The Lack of WIP Binding to Actin Results in Impaired B Cell Migration and Altered Humoral Immune Responses
Selina Jessica Keppler, Marianne Burbage, Francesca Gasparrini, et al.
Clinical Immunology (Orlando, Fla.)
|
August 20, 2016
Mutations in pyrin masquerading as a primary immunodeficiency
Yousef R Badran, Mariam Rajab, Rima Hanna-Wakim, et al.
Clinical Immunology (Orlando, Fla.)
|
May 22, 2014
A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity
Nurşen C Günaydin, Janet Chou, Neslihan E Karaca, et al.
Blood Advances
|
January 4, 2018
Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCT
Angela R Smith, Ioanna A Rota, Stefano Maio, et al.
Clinical Immunology (Orlando, Fla.)
|
August 20, 2020
Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon
Rana Mansour, Youmna El-Orfali, Antoine Saber, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 73) with videos related to
Sort By:
Page
of 8
Clinical Immunology (Orlando, Fla.)
|
March 13, 2019
Rethinking newborn screening for severe combined immunodeficiency: Lessons from an international partnership for patients with primary immunodeficiencies in Pakistan
Jacqueline G Wallace, Hamid Nawaz Tipu, Kelsey Stafstrom, et al.
Frontiers in Immunology
|
April 14, 2022
Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7Rα Chain
Rana Mansour, Yasmin El Bsat, Anthony Fadel, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 15, 2015
The Rho GTPase Cdc42 Is Essential for the Activation and Function of Mature B Cells
Natalija Gerasimcik, Carin I M Dahlberg, Marisa A P Baptista, et al.
Frontiers in Immunology
|
February 6, 2025
Deciphering the role of IL17RA in psoriasis and chronic mucocutaneous candidiasis: shared pathways and distinct manifestations
Ayat Kadhi, Edward Eid, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology
|
March 8, 2011
A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding
Michel J Massaad, Narayanaswamy Ramesh, Severine Le Bras, et al.
Cell Reports
|
July 19, 2018
The Lack of WIP Binding to Actin Results in Impaired B Cell Migration and Altered Humoral Immune Responses
Selina Jessica Keppler, Marianne Burbage, Francesca Gasparrini, et al.
Clinical Immunology (Orlando, Fla.)
|
August 20, 2016
Mutations in pyrin masquerading as a primary immunodeficiency
Yousef R Badran, Mariam Rajab, Rima Hanna-Wakim, et al.
Clinical Immunology (Orlando, Fla.)
|
May 22, 2014
A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity
Nurşen C Günaydin, Janet Chou, Neslihan E Karaca, et al.
Blood Advances
|
January 4, 2018
Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCT
Angela R Smith, Ioanna A Rota, Stefano Maio, et al.
Clinical Immunology (Orlando, Fla.)
|
August 20, 2020
Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon
Rana Mansour, Youmna El-Orfali, Antoine Saber, et al.
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of 8