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American Journal of Human Genetics
|
May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
Gabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
IL-16 production is a mechanism of resistance to BTK inhibitors and R-CHOP in lymphomas
Alberto J Arribas, Francesca Guidetti, Eleonora Cannas, et al.
Annals of Neurology
|
October 12, 2012
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
Peter K Gregersen, Roman Kosoy, Annette T Lee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 10, 2015
Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas
Ryan D Morin, Sarit Assouline, Miguel Alcaide, et al.
The Journal of Experimental Medicine
|
December 25, 2016
Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency
Hassan Abolhassani, Emily S J Edwards, Aydan Ikinciogullari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases
, John D Rioux, Philippe Goyette, et al.
The Journal of Experimental Medicine
|
September 1, 2020
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
Angela Helfricht, Peter E Thijssen, Magdalena B Rother, et al.
Blood
|
May 29, 2026
IL-16 production is a mechanism of resistance to BTK inhibitors and R-CHOP in lymphomas
Alberto J Arribas, Eleonora Cannas, Giulio Sartori, et al.
Blood
|
November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 11, 2024
Germline <i>BARD1</i> variants predispose to mesothelioma by impairing DNA repair and calcium signaling
Flavia Novelli, Yoshie Yoshikawa, Veronica Angela Maria Vitto, et al.
Page
of 53
Search research articles
Search
Showing results (491-500 of 528) with videos related to
Sort By:
Page
of 53
American Journal of Human Genetics
|
May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
Gabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
IL-16 production is a mechanism of resistance to BTK inhibitors and R-CHOP in lymphomas
Alberto J Arribas, Francesca Guidetti, Eleonora Cannas, et al.
Annals of Neurology
|
October 12, 2012
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
Peter K Gregersen, Roman Kosoy, Annette T Lee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 10, 2015
Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas
Ryan D Morin, Sarit Assouline, Miguel Alcaide, et al.
The Journal of Experimental Medicine
|
December 25, 2016
Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency
Hassan Abolhassani, Emily S J Edwards, Aydan Ikinciogullari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases
, John D Rioux, Philippe Goyette, et al.
The Journal of Experimental Medicine
|
September 1, 2020
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
Angela Helfricht, Peter E Thijssen, Magdalena B Rother, et al.
Blood
|
May 29, 2026
IL-16 production is a mechanism of resistance to BTK inhibitors and R-CHOP in lymphomas
Alberto J Arribas, Eleonora Cannas, Giulio Sartori, et al.
Blood
|
November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 11, 2024
Germline <i>BARD1</i> variants predispose to mesothelioma by impairing DNA repair and calcium signaling
Flavia Novelli, Yoshie Yoshikawa, Veronica Angela Maria Vitto, et al.
Page
of 53