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Blood
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July 4, 2007
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
Françoise Bernaudin, Gérard Socie, Mathieu Kuentz, et al.
The Journal of Allergy and Clinical Immunology
|
June 30, 2023
Actin dynamics regulation by TTC7A/PI4KIIIα limits DNA damage and cell death under confinement
Tania Gajardo, Mathilde Bernard, Marie Lô, et al.
Blood
|
October 4, 2003
Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002
Andrew R Gennery, Khulood Khawaja, Paul Veys, et al.
Blood
|
September 3, 2011
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation
Bénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, et al.
Nature Communications
|
March 3, 2026
Pharmacological stabilization of hypoxia-inducible factor 1-α dampens the interferon response and promotes glycolysis in Aicardi-Goutières syndrome
Maxime Batignes, Marine Luka, Surabhi Jagtap, et al.
Science Immunology
|
March 25, 2022
Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation
Akihiro Hoshino, David Boutboul, Yuan Zhang, et al.
Science Advances
|
October 17, 2025
Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migration
Pierre Duquesne, Céline Aoun, Mathieu Kurowska, et al.
The Journal of Allergy and Clinical Immunology
|
September 2, 2014
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
Roxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, et al.
Frontiers in Immunology
|
May 9, 2012
Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency
Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, et al.
The Journal of Clinical Investigation
|
November 4, 2009
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
Marjorie Côte, Mickaël M Ménager, Agathe Burgess, et al.
Page
of 50
Search research articles
Search
Showing results (381-390 of 493) with videos related to
Sort By:
Page
of 50
Blood
|
July 4, 2007
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
Françoise Bernaudin, Gérard Socie, Mathieu Kuentz, et al.
The Journal of Allergy and Clinical Immunology
|
June 30, 2023
Actin dynamics regulation by TTC7A/PI4KIIIα limits DNA damage and cell death under confinement
Tania Gajardo, Mathilde Bernard, Marie Lô, et al.
Blood
|
October 4, 2003
Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002
Andrew R Gennery, Khulood Khawaja, Paul Veys, et al.
Blood
|
September 3, 2011
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation
Bénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, et al.
Nature Communications
|
March 3, 2026
Pharmacological stabilization of hypoxia-inducible factor 1-α dampens the interferon response and promotes glycolysis in Aicardi-Goutières syndrome
Maxime Batignes, Marine Luka, Surabhi Jagtap, et al.
Science Immunology
|
March 25, 2022
Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation
Akihiro Hoshino, David Boutboul, Yuan Zhang, et al.
Science Advances
|
October 17, 2025
Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migration
Pierre Duquesne, Céline Aoun, Mathieu Kurowska, et al.
The Journal of Allergy and Clinical Immunology
|
September 2, 2014
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
Roxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, et al.
Frontiers in Immunology
|
May 9, 2012
Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency
Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, et al.
The Journal of Clinical Investigation
|
November 4, 2009
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
Marjorie Côte, Mickaël M Ménager, Agathe Burgess, et al.
Page
of 50