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Paul Gray

Showing results (51-60 of 67) with videos related to

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BMJ Open|June 22, 2026
Oral oxycodone versus sublingual buprenorphine for postoperative pain control after pelvic exenteration (PROSPER): a pilot, registry-embedded, multi-centre, double-blind, placebo-controlled, randomised controlled trialCharlotte Johnstone, Cherry Koh, Stephanie Mathieson, et al.
Nature Communications|November 3, 2015
Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicingDaniele Merico, Maian Roifman, Ulrich Braunschweig, 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.
Blood|March 10, 2012
Functional STAT3 deficiency compromises the generation of human T follicular helper cellsCindy S Ma, Danielle T Avery, Anna Chan, et al.
The Journal of Experimental Medicine|January 28, 2026
DOCK8 and STAT3 cooperate to restrain IgE-inducing T follicular helper cellsEmily R Siniscalco, Courtney Fisher, Meng-Ping Lu, et al.
The Journal of Experimental Medicine|May 6, 2015
STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and functionRobert P Wilson, Megan L Ives, Geetha Rao, et al.
The Australian Journal of Social Issues|August 1, 2022
Supporting Aboriginal and Torres Strait Islander Families to Stay Together from the Start (SAFeST Start): Urgent call to action to address crisis in infant removalsCatherine Chamberlain, Paul Gray, Debra Bennet, et al.
Science Immunology|June 19, 2021
Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiencyThomas Magg, Tsubasa Okano, Lars M Koenig, et al.
The Journal of Experimental Medicine|July 19, 2018
Germline-activating mutations in <i>PIK3CD</i> compromise B cell development and functionDanielle T Avery, Alisa Kane, Tina Nguyen, et al.
Blood Advances|June 20, 2025
Allogeneic hematopoietic stem cell transplantation for STAT3 hyper-IgE syndrome: a worldwide studyChristo Tsilifis, Johannes Raedler, Joanna Renke, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

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Pageof 7
BMJ Open|June 22, 2026
Oral oxycodone versus sublingual buprenorphine for postoperative pain control after pelvic exenteration (PROSPER): a pilot, registry-embedded, multi-centre, double-blind, placebo-controlled, randomised controlled trialCharlotte Johnstone, Cherry Koh, Stephanie Mathieson, et al.
Nature Communications|November 3, 2015
Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicingDaniele Merico, Maian Roifman, Ulrich Braunschweig, 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.
Blood|March 10, 2012
Functional STAT3 deficiency compromises the generation of human T follicular helper cellsCindy S Ma, Danielle T Avery, Anna Chan, et al.
The Journal of Experimental Medicine|January 28, 2026
DOCK8 and STAT3 cooperate to restrain IgE-inducing T follicular helper cellsEmily R Siniscalco, Courtney Fisher, Meng-Ping Lu, et al.
The Journal of Experimental Medicine|May 6, 2015
STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and functionRobert P Wilson, Megan L Ives, Geetha Rao, et al.
The Australian Journal of Social Issues|August 1, 2022
Supporting Aboriginal and Torres Strait Islander Families to Stay Together from the Start (SAFeST Start): Urgent call to action to address crisis in infant removalsCatherine Chamberlain, Paul Gray, Debra Bennet, et al.
Science Immunology|June 19, 2021
Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiencyThomas Magg, Tsubasa Okano, Lars M Koenig, et al.
The Journal of Experimental Medicine|July 19, 2018
Germline-activating mutations in <i>PIK3CD</i> compromise B cell development and functionDanielle T Avery, Alisa Kane, Tina Nguyen, et al.
Blood Advances|June 20, 2025
Allogeneic hematopoietic stem cell transplantation for STAT3 hyper-IgE syndrome: a worldwide studyChristo Tsilifis, Johannes Raedler, Joanna Renke, et al.
Pageof 7