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

Peter D Arkwright

Showing results (121-130 of 170) with videos related to

Pageof 17
Sort By:
Frontiers in Immunology|September 26, 2018
Increased Risk for Malignancies in 131 Affected <i>CTLA4</i> Mutation CarriersDavid Egg, Charlotte Schwab, Annemarie Gabrysch, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Science (New York, N.Y.)|July 21, 2018
Biallelic <i>RIPK1</i> mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammationDelphine Cuchet-Lourenço, Davide Eletto, Changxin Wu, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2016
Dedicator of cytokinesis 8-deficient CD4<sup>+</sup> T cells are biased to a T<sub>H</sub>2 effector fate at the expense of T<sub>H</sub>1 and T<sub>H</sub>17 cellsStuart G Tangye, Bethany Pillay, Katrina L Randall, et al.
Gastro Hep Advances|November 14, 2025
Whole Exome Sequencing in Children With Autoimmune Hepatitis Identified Mutations in Genes Involved in the mTORC1 Signaling PathwayLéa-Philippine Gaigne, Caroline Besnard, Orianne Debeaupuis, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2008
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type IAntonella Meloni, Maria Furcas, Filomena Cetani, et al.
Plos Genetics|August 29, 2006
Novel STAT1 alleles in otherwise healthy patients with mycobacterial diseaseAriane Chapgier, Stéphanie Boisson-Dupuis, Emmanuelle Jouanguy, et al.
Blood|September 25, 2012
IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patientsSandra Weller, Mélanie Bonnet, Héloïse Delagreverie, et al.
Blood|April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndromeSimon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Nature Genetics|April 4, 2017
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytesMaximilian Witzel, Daniel Petersheim, Yanxin Fan, et al.
Pageof 17

Showing results (121-130 of 170) with videos related to

Sort By:
Pageof 17
Frontiers in Immunology|September 26, 2018
Increased Risk for Malignancies in 131 Affected <i>CTLA4</i> Mutation CarriersDavid Egg, Charlotte Schwab, Annemarie Gabrysch, et al.
JCI Insight|March 13, 2020
Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutationEmmanuel Martin, Norbert Minet, Anne-Claire Boschat, et al.
Science (New York, N.Y.)|July 21, 2018
Biallelic <i>RIPK1</i> mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammationDelphine Cuchet-Lourenço, Davide Eletto, Changxin Wu, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2016
Dedicator of cytokinesis 8-deficient CD4<sup>+</sup> T cells are biased to a T<sub>H</sub>2 effector fate at the expense of T<sub>H</sub>1 and T<sub>H</sub>17 cellsStuart G Tangye, Bethany Pillay, Katrina L Randall, et al.
Gastro Hep Advances|November 14, 2025
Whole Exome Sequencing in Children With Autoimmune Hepatitis Identified Mutations in Genes Involved in the mTORC1 Signaling PathwayLéa-Philippine Gaigne, Caroline Besnard, Orianne Debeaupuis, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2008
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type IAntonella Meloni, Maria Furcas, Filomena Cetani, et al.
Plos Genetics|August 29, 2006
Novel STAT1 alleles in otherwise healthy patients with mycobacterial diseaseAriane Chapgier, Stéphanie Boisson-Dupuis, Emmanuelle Jouanguy, et al.
Blood|September 25, 2012
IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patientsSandra Weller, Mélanie Bonnet, Héloïse Delagreverie, et al.
Blood|April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndromeSimon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Nature Genetics|April 4, 2017
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytesMaximilian Witzel, Daniel Petersheim, Yanxin Fan, et al.
Pageof 17