Angela Grainger - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Angela Grainger

Showing results (21-30 of 23) with videos related to

Pageof 3

Sort By:

You have reached the last page of results.This site can display upto 23 results.

Annals of the Rheumatic Diseases|June 30, 2017

Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)Christopher J A Duncan, Emma Dinnigan, Rachel Theobald, et al.

Journal of Clinical Immunology|November 4, 2016

Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome SequencingKarin R Engelhardt, Yaobo Xu, Angela Grainger, et al.

Science Immunology|December 15, 2019

Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.

Pageof 3

Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 23 results.

Annals of the Rheumatic Diseases|June 30, 2017

Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)Christopher J A Duncan, Emma Dinnigan, Rachel Theobald, et al.

Journal of Clinical Immunology|November 4, 2016

Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome SequencingKarin R Engelhardt, Yaobo Xu, Angela Grainger, et al.

Science Immunology|December 15, 2019

Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.

Pageof 3