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

Raphael Carapito

Showing results (31-40 of 79) with videos related to

Pageof 8
Sort By:
Matrix Biology : Journal of the International Society for Matrix Biology|January 20, 2023
Infiltrating CD8+ T cells and M2 macrophages are retained in tumor matrix tracks enriched in low tension fibronectin fibersCharlotte M Fonta, Thomas Loustau, Chengbei Li, et al.
Bioinformatics (Oxford, England)|April 4, 2019
HLA*LA-HLA typing from linearly projected graph alignmentsAlexander T Dilthey, Alexander J Mentzer, Raphael Carapito, et al.
Frontiers in Immunology|March 11, 2020
High-Throughput <i>MICA/B</i> Genotyping of Over Two Million Samples: Workflow and Allele FrequenciesAnja Klussmeier, Carolin Massalski, Kathrin Putke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystoniaRaphael Carapito, Nicodème Paul, Meiggie Untrau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex DystoniaAmjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Plos Pathogens|October 19, 2018
An unusually high substitution rate in transplant-associated BK polyomavirus in vivo is further concentrated in HLA-C-bound viral peptidesPilar Domingo-Calap, Benjamin Schubert, Mélanie Joly, et al.
Blood|November 23, 2020
SRP54 mutations induce congenital neutropenia via dominant-negative effects on XBP1 splicingChristoph Schürch, Thorsten Schaefer, Joëlle S Müller, et al.
Scandinavian Journal of Immunology|June 27, 2023
Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patientShaghayegh Tajik, Mohsen Badalzadeh, Massoud Houshmand, et al.
BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Blood Cancer Journal|August 9, 2023
Multiomics of three hematological malignancies in a patient reveal their origin from clonal hematopoietic stem cellsSylvain Mayeur, Anne Molitor, Laurent Miguet, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Matrix Biology : Journal of the International Society for Matrix Biology|January 20, 2023
Infiltrating CD8+ T cells and M2 macrophages are retained in tumor matrix tracks enriched in low tension fibronectin fibersCharlotte M Fonta, Thomas Loustau, Chengbei Li, et al.
Bioinformatics (Oxford, England)|April 4, 2019
HLA*LA-HLA typing from linearly projected graph alignmentsAlexander T Dilthey, Alexander J Mentzer, Raphael Carapito, et al.
Frontiers in Immunology|March 11, 2020
High-Throughput <i>MICA/B</i> Genotyping of Over Two Million Samples: Workflow and Allele FrequenciesAnja Klussmeier, Carolin Massalski, Kathrin Putke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystoniaRaphael Carapito, Nicodème Paul, Meiggie Untrau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex DystoniaAmjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Plos Pathogens|October 19, 2018
An unusually high substitution rate in transplant-associated BK polyomavirus in vivo is further concentrated in HLA-C-bound viral peptidesPilar Domingo-Calap, Benjamin Schubert, Mélanie Joly, et al.
Blood|November 23, 2020
SRP54 mutations induce congenital neutropenia via dominant-negative effects on XBP1 splicingChristoph Schürch, Thorsten Schaefer, Joëlle S Müller, et al.
Scandinavian Journal of Immunology|June 27, 2023
Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patientShaghayegh Tajik, Mohsen Badalzadeh, Massoud Houshmand, et al.
BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Blood Cancer Journal|August 9, 2023
Multiomics of three hematological malignancies in a patient reveal their origin from clonal hematopoietic stem cellsSylvain Mayeur, Anne Molitor, Laurent Miguet, et al.
Pageof 8