Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alain Fischer

Showing results (321-330 of 493) with videos related to

Pageof 50
Sort By:
Pediatrics|June 4, 2002
Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his motherSophie Dupuis-Girod, Nadège Corradini, Smail Hadj-Rabia, et al.
Nature Communications|March 7, 2015
Corrigendum: Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defectMarkus Bender, Simon Stritt, Paquita Nurden, et al.
Haematologica|October 15, 2020
Safety and efficacy of brentuximab vedotin as a treatment for lymphoproliferative disorders in primary immunodeficienciesThomas Pincez, Julie Bruneau, Laureline Berteloot, et al.
Journal of Clinical Immunology|January 11, 2021
Life-Saving, Dose-Adjusted, Targeted Therapy in a Patient with a STAT3 Gain-of-Function MutationEytan Sarfati, Jérome Hadjadj, Mathieu Fusaro, et al.
Cell Discovery|November 21, 2018
Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structureMarie-Therese El-Daher, Nicolas Cagnard, Marine Gil, et al.
Nature|May 30, 2014
CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferationEmmanuel Martin, Noé Palmic, Sylvia Sanquer, et al.
The New England Journal of Medicine|April 19, 2002
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapySalima Hacein-Bey-Abina, Françoise Le Deist, Frédérique Carlier, et al.
Blood|September 22, 2005
Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicityChantal Lagresle-Peyrou, Frank Yates, Michèle Malassis-Séris, et al.
Human Mutation|November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutationsHouda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
Journal of Clinical Immunology|June 25, 2020
Correction to: A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary ImmunodeficiencyHélène Coignard-Biehler, Nizar Mahlaoui, Benoit Pilmis, et al.
Pageof 50

Showing results (321-330 of 493) with videos related to

Sort By:
Pageof 50
Pediatrics|June 4, 2002
Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his motherSophie Dupuis-Girod, Nadège Corradini, Smail Hadj-Rabia, et al.
Nature Communications|March 7, 2015
Corrigendum: Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defectMarkus Bender, Simon Stritt, Paquita Nurden, et al.
Haematologica|October 15, 2020
Safety and efficacy of brentuximab vedotin as a treatment for lymphoproliferative disorders in primary immunodeficienciesThomas Pincez, Julie Bruneau, Laureline Berteloot, et al.
Journal of Clinical Immunology|January 11, 2021
Life-Saving, Dose-Adjusted, Targeted Therapy in a Patient with a STAT3 Gain-of-Function MutationEytan Sarfati, Jérome Hadjadj, Mathieu Fusaro, et al.
Cell Discovery|November 21, 2018
Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structureMarie-Therese El-Daher, Nicolas Cagnard, Marine Gil, et al.
Nature|May 30, 2014
CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferationEmmanuel Martin, Noé Palmic, Sylvia Sanquer, et al.
The New England Journal of Medicine|April 19, 2002
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapySalima Hacein-Bey-Abina, Françoise Le Deist, Frédérique Carlier, et al.
Blood|September 22, 2005
Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicityChantal Lagresle-Peyrou, Frank Yates, Michèle Malassis-Séris, et al.
Human Mutation|November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutationsHouda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
Journal of Clinical Immunology|June 25, 2020
Correction to: A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary ImmunodeficiencyHélène Coignard-Biehler, Nizar Mahlaoui, Benoit Pilmis, et al.
Pageof 50