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Yanick J Crow

Showing results (151-160 of 234) with videos related to

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Immunity|June 15, 2024
The brain microvasculature is a primary mediator of interferon-α neurotoxicity in human cerebral interferonopathiesBarney Viengkhou, Emina Hayashida, Sarah McGlasson, et al.
Nature|July 27, 2018
Mitochondrial double-stranded RNA triggers antiviral signalling in humansAshish Dhir, Somdutta Dhir, Lukasz S Borowski, et al.
Pediatric Rheumatology Online Journal|October 4, 2014
Mutations in CECR1 associated with a neutrophil signature in peripheral bloodAlexandre Belot, Evangeline Wassmer, Marinka Twilt, et al.
Journal of Medical Genetics|November 23, 2013
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1John H Livingston, Jean-Pierre Lin, Russell C Dale, et al.
Acta Neuropathologica|February 27, 2020
Biallelic mutations in NRROS cause an early onset lethal microgliopathyColin Smith, Barry W McColl, Anirudh Patir, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Nature|November 8, 2011
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolaseDavid C Goldstone, Valerie Ennis-Adeniran, Joseph J Hedden, et al.
American Journal of Human Genetics|August 24, 2010
Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyriaMary C O'Driscoll, Sarah B Daly, Jill E Urquhart, et al.
Human Mutation|May 22, 2018
Autosomal-dominant early-onset spastic paraparesis with brain calcification due to IFIH1 gain-of-functionLyse Ruaud, Gillian I Rice, Christelle Cabrol, et al.
Human Mutation|January 30, 2009
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosisChiara Aiello, Alessandra Terracciano, Alessandro Simonati, et al.
Pageof 24

Showing results (151-160 of 234) with videos related to

Sort By:
Pageof 24
Immunity|June 15, 2024
The brain microvasculature is a primary mediator of interferon-α neurotoxicity in human cerebral interferonopathiesBarney Viengkhou, Emina Hayashida, Sarah McGlasson, et al.
Nature|July 27, 2018
Mitochondrial double-stranded RNA triggers antiviral signalling in humansAshish Dhir, Somdutta Dhir, Lukasz S Borowski, et al.
Pediatric Rheumatology Online Journal|October 4, 2014
Mutations in CECR1 associated with a neutrophil signature in peripheral bloodAlexandre Belot, Evangeline Wassmer, Marinka Twilt, et al.
Journal of Medical Genetics|November 23, 2013
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1John H Livingston, Jean-Pierre Lin, Russell C Dale, et al.
Acta Neuropathologica|February 27, 2020
Biallelic mutations in NRROS cause an early onset lethal microgliopathyColin Smith, Barry W McColl, Anirudh Patir, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Nature|November 8, 2011
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolaseDavid C Goldstone, Valerie Ennis-Adeniran, Joseph J Hedden, et al.
American Journal of Human Genetics|August 24, 2010
Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyriaMary C O'Driscoll, Sarah B Daly, Jill E Urquhart, et al.
Human Mutation|May 22, 2018
Autosomal-dominant early-onset spastic paraparesis with brain calcification due to IFIH1 gain-of-functionLyse Ruaud, Gillian I Rice, Christelle Cabrol, et al.
Human Mutation|January 30, 2009
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosisChiara Aiello, Alessandra Terracciano, Alessandro Simonati, et al.
Pageof 24