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The Journal of Allergy and Clinical Immunology
|
July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation
Tangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
Blood
|
January 10, 2022
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects
Laëtitia Kermasson, Dmitri Churikov, Aya Awad, et al.
The Journal of Infectious Diseases
|
April 6, 2013
Genotoxic signature in cord blood cells of newborns exposed in utero to a Zidovudine-based antiretroviral combination
Isabelle André-Schmutz, Liliane Dal-Cortivo, Emmanuelle Six, et al.
The Journal of Experimental Medicine
|
February 8, 2012
Cernunnos influences human immunoglobulin class switch recombination and may be associated with B cell lymphomagenesis
Likun Du, Roujun Peng, Andrea Björkman, et al.
Blood
|
June 2, 2019
EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency
Marta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Clinical Investigation
|
January 23, 2025
Human oncostatin M deficiency underlies an inherited severe bone marrow failure syndrome
Alexandrine Garrigue, Laëtitia Kermasson, Sandrine Susini, et al.
Genes & Development
|
September 4, 2024
Heterozygous <i>RPA2</i> variant as a novel genetic cause of telomere biology disorders
Rima Kochman, Ibrahima Ba, Maïlyn Yates, et al.
Blood Cancer Journal
|
November 5, 2025
Telomere occupancy by TRF2 is altered by KIT mutations and correlates with mastocytosis regression
Julie Bruneau, Sophie Georgin-Lavialle, Sophia Ladraa, et al.
Human Molecular Genetics
|
January 28, 2020
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome
Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, et al.
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of 10
Search research articles
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Showing results (71-80 of 94) with videos related to
Sort By:
Page
of 10
The Journal of Allergy and Clinical Immunology
|
July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation
Tangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
Blood
|
January 10, 2022
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects
Laëtitia Kermasson, Dmitri Churikov, Aya Awad, et al.
The Journal of Infectious Diseases
|
April 6, 2013
Genotoxic signature in cord blood cells of newborns exposed in utero to a Zidovudine-based antiretroviral combination
Isabelle André-Schmutz, Liliane Dal-Cortivo, Emmanuelle Six, et al.
The Journal of Experimental Medicine
|
February 8, 2012
Cernunnos influences human immunoglobulin class switch recombination and may be associated with B cell lymphomagenesis
Likun Du, Roujun Peng, Andrea Björkman, et al.
Blood
|
June 2, 2019
EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, et al.
The Journal of Clinical Investigation
|
September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency
Marta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Clinical Investigation
|
January 23, 2025
Human oncostatin M deficiency underlies an inherited severe bone marrow failure syndrome
Alexandrine Garrigue, Laëtitia Kermasson, Sandrine Susini, et al.
Genes & Development
|
September 4, 2024
Heterozygous <i>RPA2</i> variant as a novel genetic cause of telomere biology disorders
Rima Kochman, Ibrahima Ba, Maïlyn Yates, et al.
Blood Cancer Journal
|
November 5, 2025
Telomere occupancy by TRF2 is altered by KIT mutations and correlates with mastocytosis regression
Julie Bruneau, Sophie Georgin-Lavialle, Sophia Ladraa, et al.
Human Molecular Genetics
|
January 28, 2020
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome
Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, et al.
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of 10