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Haifa H Jabara

Showing results (11-20 of 15) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|February 18, 2014
TRIF signaling is essential for TLR4-driven IgE class switchingErin Janssen, Esra Ozcan, Kyriaki Liadaki, et al.
The Journal of Allergy and Clinical Immunology|September 10, 2016
Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in miceHaifa H Jabara, John J Lee, Erin Janssen, et al.
The Journal of Allergy and Clinical Immunology|June 4, 2013
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiencyHaifa H Jabara, Toshiro Ohsumi, Janet Chou, et al.
Nature Immunology|May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Journal of Immunology (Baltimore, Md. : 1950)|February 18, 2014
TRIF signaling is essential for TLR4-driven IgE class switchingErin Janssen, Esra Ozcan, Kyriaki Liadaki, et al.
The Journal of Allergy and Clinical Immunology|September 10, 2016
Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in miceHaifa H Jabara, John J Lee, Erin Janssen, et al.
The Journal of Allergy and Clinical Immunology|June 4, 2013
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiencyHaifa H Jabara, Toshiro Ohsumi, Janet Chou, et al.
Nature Immunology|May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
Pageof 2