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Ismail Reisli

Showing results (101-110 of 139) with videos related to

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Immunologic Research|October 20, 2021
Correction to: Primary antibody deficiencies in Turkey: molecular and clinical aspectsSinem Firtina, Yuk Yin Ng, Ozden H Ng, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Multicentric analysis of childhood tuberculosis in TurkeySevgi Pekcan, Ayşe Tana Aslan, Nural Kiper, et al.
International Journal of Immunogenetics|May 24, 2020
Mutational landscape of severe combined immunodeficiency patients from TurkeySinem Firtina, Yuk Yin Ng, Ozden Hatirnaz Ng, et al.
Blood|April 15, 2018
Patients with <i>CD3G</i> mutations reveal a role for human CD3γ in T<sub>reg</sub> diversity and suppressive functionJared H Rowe, Ottavia M Delmonte, Sevgi Keles, et al.
The Journal of Allergy and Clinical Immunology|November 21, 2017
Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiencyErsin Gul, Esra Hazar Sayar, Bilgi Gungor, et al.
The Journal of Allergy and Clinical Immunology|July 7, 2009
Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndromeShadi Al Khatib, Sevgi Keles, Maria Garcia-Lloret, et al.
Journal of Clinical Immunology|July 28, 2023
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic DermatitisNurhan Kasap, Altan Kara, Velat Celik, et al.
Human Molecular Genetics|October 18, 2015
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiencyTimo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Clinical Immunology (Orlando, Fla.)|July 11, 2023
Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1Serife Erdem, Sule Haskologlu, Yesim Haliloglu, et al.
Nature Immunology|March 25, 2022
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Pageof 14

Showing results (101-110 of 139) with videos related to

Sort By:
Pageof 14
Immunologic Research|October 20, 2021
Correction to: Primary antibody deficiencies in Turkey: molecular and clinical aspectsSinem Firtina, Yuk Yin Ng, Ozden H Ng, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Multicentric analysis of childhood tuberculosis in TurkeySevgi Pekcan, Ayşe Tana Aslan, Nural Kiper, et al.
International Journal of Immunogenetics|May 24, 2020
Mutational landscape of severe combined immunodeficiency patients from TurkeySinem Firtina, Yuk Yin Ng, Ozden Hatirnaz Ng, et al.
Blood|April 15, 2018
Patients with <i>CD3G</i> mutations reveal a role for human CD3γ in T<sub>reg</sub> diversity and suppressive functionJared H Rowe, Ottavia M Delmonte, Sevgi Keles, et al.
The Journal of Allergy and Clinical Immunology|November 21, 2017
Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiencyErsin Gul, Esra Hazar Sayar, Bilgi Gungor, et al.
The Journal of Allergy and Clinical Immunology|July 7, 2009
Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndromeShadi Al Khatib, Sevgi Keles, Maria Garcia-Lloret, et al.
Journal of Clinical Immunology|July 28, 2023
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic DermatitisNurhan Kasap, Altan Kara, Velat Celik, et al.
Human Molecular Genetics|October 18, 2015
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiencyTimo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Clinical Immunology (Orlando, Fla.)|July 11, 2023
Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1Serife Erdem, Sule Haskologlu, Yesim Haliloglu, et al.
Nature Immunology|March 25, 2022
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Pageof 14