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 (11-20 of 79) with videos related to

Pageof 8
Sort By:
STAR Protocols|July 2, 2023
Measuring the transcriptome-wide effects of aging on murine adipocytes using RNAseqAurore De Cauwer, Angélique Pichot, Anne Molitor, et al.
Chemical Communications (Cambridge, England)|July 21, 2011
α-L-Arabinofuranosylated pyrrolidines as arabinanase inhibitorsEthan D Goddard-Borger, Raphael Carapito, Jean-Marc Jeltsch, et al.
RMD Open|March 16, 2016
Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)Laurent Messer, Ghada Alsaleh, Philippe Georgel, et al.
Frontiers in Immunology|January 11, 2020
Update on Fc-Mediated Antibody Functions Against HIV-1 Beyond NeutralizationBin Su, Stefania Dispinseri, Valeria Iannone, et al.
RMD Open|November 2, 2021
Contrasting role of <i>NLRP12</i> in autoinflammation: evidence from a case report and mouse modelsDan Lévy, Alexandre Mariotte, Aurore DeCauwer, et al.
Cold Spring Harbor Molecular Case Studies|May 9, 2023
Genomic profiling of a metastatic anaplastic melanocytic neuroectodermal tumor arising from a mature thymic teratoma as part of a mediastinal germ cell tumorSylvain Mayeur, Benoit Lhermitte, Justine Gantzer, et al.
Journal of Human Genetics|May 10, 2019
Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitisAnne Molitor, Tony Prud'homme, Zhichao Miao, et al.
Structure (London, England : 1993)|October 14, 2020
Structural and Functional Impact of SRP54 Mutations Causing Severe Congenital NeutropeniaKeven D Juaire, Karine Lapouge, Matthias M M Becker, et al.
Iscience|October 3, 2022
<i>Dicer1</i> deficient mice exhibit premature aging and metabolic perturbations in adipocytesAurore De Cauwer, Thomas Loustau, William Erne, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
STAR Protocols|July 2, 2023
Measuring the transcriptome-wide effects of aging on murine adipocytes using RNAseqAurore De Cauwer, Angélique Pichot, Anne Molitor, et al.
Chemical Communications (Cambridge, England)|July 21, 2011
α-L-Arabinofuranosylated pyrrolidines as arabinanase inhibitorsEthan D Goddard-Borger, Raphael Carapito, Jean-Marc Jeltsch, et al.
RMD Open|March 16, 2016
Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)Laurent Messer, Ghada Alsaleh, Philippe Georgel, et al.
Frontiers in Immunology|January 11, 2020
Update on Fc-Mediated Antibody Functions Against HIV-1 Beyond NeutralizationBin Su, Stefania Dispinseri, Valeria Iannone, et al.
RMD Open|November 2, 2021
Contrasting role of <i>NLRP12</i> in autoinflammation: evidence from a case report and mouse modelsDan Lévy, Alexandre Mariotte, Aurore DeCauwer, et al.
Cold Spring Harbor Molecular Case Studies|May 9, 2023
Genomic profiling of a metastatic anaplastic melanocytic neuroectodermal tumor arising from a mature thymic teratoma as part of a mediastinal germ cell tumorSylvain Mayeur, Benoit Lhermitte, Justine Gantzer, et al.
Journal of Human Genetics|May 10, 2019
Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitisAnne Molitor, Tony Prud'homme, Zhichao Miao, et al.
Structure (London, England : 1993)|October 14, 2020
Structural and Functional Impact of SRP54 Mutations Causing Severe Congenital NeutropeniaKeven D Juaire, Karine Lapouge, Matthias M M Becker, et al.
Iscience|October 3, 2022
<i>Dicer1</i> deficient mice exhibit premature aging and metabolic perturbations in adipocytesAurore De Cauwer, Thomas Loustau, William Erne, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Pageof 8