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Pedro Gonzalez

Showing results (241-250 of 248) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
American Journal of Human Genetics|November 4, 2008
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndromeAlexander G Bassuk, Robyn H Wallace, Aimee Buhr, et al.
Blood|February 3, 2023
Arginine metabolism regulates human erythroid differentiation through hypusination of eIF5APedro Gonzalez-Menendez, Ira Phadke, Meagan E Olive, et al.
Investigative Ophthalmology & Visual Science|August 19, 2016
A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD ConsortiumYutao Liu, Jessica Cooke Bailey, Inas Helwa, et al.
Experimental Eye Research|March 13, 2018
Consensus recommendations for trabecular meshwork cell isolation, characterization and cultureKate E Keller, Sanjoy K Bhattacharya, Theresa Borrás, et al.
Epilepsia|July 2, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variantsClaudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga, et al.
The Lancet. Neurology|October 25, 2020
Monogenic variants in dystonia: an exome-wide sequencing studyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Translational Lung Cancer Research|May 22, 2026
International Consensus on Severe Lung Cancer-The Second EditionXinqing Lin, Qian Chu, Yuchao Dong, et al.
Pageof 25

Showing results (241-250 of 248) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 248 results.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
American Journal of Human Genetics|November 4, 2008
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndromeAlexander G Bassuk, Robyn H Wallace, Aimee Buhr, et al.
Blood|February 3, 2023
Arginine metabolism regulates human erythroid differentiation through hypusination of eIF5APedro Gonzalez-Menendez, Ira Phadke, Meagan E Olive, et al.
Investigative Ophthalmology & Visual Science|August 19, 2016
A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD ConsortiumYutao Liu, Jessica Cooke Bailey, Inas Helwa, et al.
Experimental Eye Research|March 13, 2018
Consensus recommendations for trabecular meshwork cell isolation, characterization and cultureKate E Keller, Sanjoy K Bhattacharya, Theresa Borrás, et al.
Epilepsia|July 2, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variantsClaudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga, et al.
The Lancet. Neurology|October 25, 2020
Monogenic variants in dystonia: an exome-wide sequencing studyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Translational Lung Cancer Research|May 22, 2026
International Consensus on Severe Lung Cancer-The Second EditionXinqing Lin, Qian Chu, Yuchao Dong, et al.
Pageof 25