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Yanick J Crow

Showing results (131-140 of 234) with videos related to

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The EMBO Journal|July 23, 2013
SAMHD1-dependent retroviral control and escape in miceJan Rehwinkel, Jonathan Maelfait, Anne Bridgeman, et al.
The Journal of Experimental Medicine|April 3, 2019
Bloom syndrome protein restrains innate immune sensing of micronuclei by cGASMatthieu Gratia, Mathieu P Rodero, Cécile Conrad, et al.
Brain : a Journal of Neurology|October 19, 2018
A child with severe juvenile dermatomyositis treated with ruxolitinibFlorence A Aeschlimann, Marie-Louise Frémond, Darragh Duffy, et al.
Rheumatology (Oxford, England)|January 24, 2020
Inhibition of IFNα secretion in cells from patients with juvenile dermatomyositis under TBK1 inhibitor treatment revealed by single-molecular assay technologyCyril Gitiaux, Vincent Bondet, Nassima Bekaddour, et al.
EMBO Reports|March 25, 2025
Distinct pathogenic mutations in ARF1 allow dissection of its dual role in cGAS-STING signallingJohannes Lang, Tim Bergner, Julia Zinngrebe, et al.
Journal of Child Neurology|December 24, 2014
Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern RecognitionAdeline Vanderver, Morgan Prust, Nadja Kadom, et al.
American Journal of Human Genetics|January 27, 2015
A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndromeFrank Rutsch, Mary MacDougall, Changming Lu, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Congenital glaucoma and brain stem atrophy as features of Aicardi-Goutières syndromeYanick J Crow, R F Massey, J R Innes, et al.
Neuropediatrics|November 29, 2019
Biallelic Mutations in MTPAP Associated with a Lethal EncephalopathyLien Van Eyck, Francesco Bruni, Anne Ronan, et al.
American Journal of Human Genetics|March 16, 2007
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndromeGillian Rice, William G Newman, John Dean, et al.
Pageof 24

Showing results (131-140 of 234) with videos related to

Sort By:
Pageof 24
The EMBO Journal|July 23, 2013
SAMHD1-dependent retroviral control and escape in miceJan Rehwinkel, Jonathan Maelfait, Anne Bridgeman, et al.
The Journal of Experimental Medicine|April 3, 2019
Bloom syndrome protein restrains innate immune sensing of micronuclei by cGASMatthieu Gratia, Mathieu P Rodero, Cécile Conrad, et al.
Brain : a Journal of Neurology|October 19, 2018
A child with severe juvenile dermatomyositis treated with ruxolitinibFlorence A Aeschlimann, Marie-Louise Frémond, Darragh Duffy, et al.
Rheumatology (Oxford, England)|January 24, 2020
Inhibition of IFNα secretion in cells from patients with juvenile dermatomyositis under TBK1 inhibitor treatment revealed by single-molecular assay technologyCyril Gitiaux, Vincent Bondet, Nassima Bekaddour, et al.
EMBO Reports|March 25, 2025
Distinct pathogenic mutations in ARF1 allow dissection of its dual role in cGAS-STING signallingJohannes Lang, Tim Bergner, Julia Zinngrebe, et al.
Journal of Child Neurology|December 24, 2014
Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern RecognitionAdeline Vanderver, Morgan Prust, Nadja Kadom, et al.
American Journal of Human Genetics|January 27, 2015
A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndromeFrank Rutsch, Mary MacDougall, Changming Lu, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Congenital glaucoma and brain stem atrophy as features of Aicardi-Goutières syndromeYanick J Crow, R F Massey, J R Innes, et al.
Neuropediatrics|November 29, 2019
Biallelic Mutations in MTPAP Associated with a Lethal EncephalopathyLien Van Eyck, Francesco Bruni, Anne Ronan, et al.
American Journal of Human Genetics|March 16, 2007
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndromeGillian Rice, William G Newman, John Dean, et al.
Pageof 24