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Alan Pittman

Showing results (41-50 of 55) with videos related to

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Brain : a Journal of Neurology|March 24, 2017
Clinical and genetic characterization of leukoencephalopathies in adultsDavid S Lynch, Anderson Rodrigues Brandão de Paiva, Wei Jia Zhang, et al.
Brain : a Journal of Neurology|September 8, 2022
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 lociMarc P M Soutar, Daniela Melandri, Benjamin O'Callaghan, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Frontiers in Global Women'S Health|July 9, 2026
The lipedema common case report form as a research tool: standardizing lipedema data collectionStephanie Galia, Rachelle Crescenzi, Philipp Kruppa, et al.
The Journal of Clinical Investigation|February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystoniaNiccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.
Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.
American Journal of Human Genetics|March 7, 2020
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain CalcificationLucia V Schottlaender, Rosella Abeti, Zane Jaunmuktane, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
The Journal of Clinical Investigation|February 21, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapyLara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
Gut|April 12, 2012
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individualsMalcolm G Dunlop, Albert Tenesa, Susan M Farrington, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Brain : a Journal of Neurology|March 24, 2017
Clinical and genetic characterization of leukoencephalopathies in adultsDavid S Lynch, Anderson Rodrigues Brandão de Paiva, Wei Jia Zhang, et al.
Brain : a Journal of Neurology|September 8, 2022
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 lociMarc P M Soutar, Daniela Melandri, Benjamin O'Callaghan, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Frontiers in Global Women'S Health|July 9, 2026
The lipedema common case report form as a research tool: standardizing lipedema data collectionStephanie Galia, Rachelle Crescenzi, Philipp Kruppa, et al.
The Journal of Clinical Investigation|February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystoniaNiccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.
Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.
American Journal of Human Genetics|March 7, 2020
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain CalcificationLucia V Schottlaender, Rosella Abeti, Zane Jaunmuktane, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
The Journal of Clinical Investigation|February 21, 2018
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapyLara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
Gut|April 12, 2012
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individualsMalcolm G Dunlop, Albert Tenesa, Susan M Farrington, et al.
Pageof 6