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Raphael Carapito

Showing results (61-70 of 79) with videos related to

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Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|July 26, 2023
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patientsMohammad Reza Fazlollahi, Amir Ali Hamidieh, Leila Moradi, et al.
Cancer Immunology Research|July 16, 2020
Tenascin-C Orchestrates an Immune-Suppressive Tumor Microenvironment in Oral Squamous Cell CarcinomaCaroline Spenlé, Thomas Loustau, Devadarssen Murdamoothoo, et al.
Nature Medicine|March 15, 2022
The MHC class I MICA gene is a histocompatibility antigen in kidney transplantationRaphael Carapito, Ismail Aouadi, Martin Verniquet, et al.
European Journal of Human Genetics : EJHG|December 31, 2024
RICTOR variants are associated with neurodevelopmental disordersRaphael Carapito, Anne Molitor, Lisa Pavinato, et al.
Journal of Human Immunity|November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiencyTristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
Bone Marrow Transplantation|April 15, 2020
Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV statusRaphael Carapito, Ismail Aouadi, Angélique Pichot, et al.
American Journal of Human Genetics|December 17, 2022
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
American Journal of Human Genetics|March 3, 2023
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, et al.
Blood|August 24, 2016
Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHDRaphael Carapito, Nicolas Jung, Marius Kwemou, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|July 26, 2023
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patientsMohammad Reza Fazlollahi, Amir Ali Hamidieh, Leila Moradi, et al.
Cancer Immunology Research|July 16, 2020
Tenascin-C Orchestrates an Immune-Suppressive Tumor Microenvironment in Oral Squamous Cell CarcinomaCaroline Spenlé, Thomas Loustau, Devadarssen Murdamoothoo, et al.
Nature Medicine|March 15, 2022
The MHC class I MICA gene is a histocompatibility antigen in kidney transplantationRaphael Carapito, Ismail Aouadi, Martin Verniquet, et al.
European Journal of Human Genetics : EJHG|December 31, 2024
RICTOR variants are associated with neurodevelopmental disordersRaphael Carapito, Anne Molitor, Lisa Pavinato, et al.
Journal of Human Immunity|November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiencyTristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
Bone Marrow Transplantation|April 15, 2020
Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV statusRaphael Carapito, Ismail Aouadi, Angélique Pichot, et al.
American Journal of Human Genetics|December 17, 2022
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
American Journal of Human Genetics|March 3, 2023
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, et al.
Blood|August 24, 2016
Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHDRaphael Carapito, Nicolas Jung, Marius Kwemou, et al.
Pageof 8