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Showing results (381-390 of 396) with videos related to

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BMJ Open|June 18, 2026
Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profileAnjali K Henders, Laura Ziser, Fleur C Garton, et al.
Brain : a Journal of Neurology|March 19, 2020
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosisCarol Dobson-Stone, Marianne Hallupp, Hamideh Shahheydari, et al.
Ophthalmology|May 26, 2016
Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter StudyYoshihiro Yonekawa, Wei-Chi Wu, Shunji Kusaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2011
A yeast functional screen predicts new candidate ALS disease genesJulien Couthouis, Michael P Hart, James Shorter, et al.
Ophthalmology. Retina|November 29, 2024
Clinical Characteristics and Treatment Outcomes in Unilateral Coats Disease: A Global Collaborative StudyAndrew S H Tsai, Chung-Ting Wang, Thomas C Lee, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|September 22, 2017
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBeben Benyamin, Ji He, Qiongyi Zhao, et al.
Nature Communications|April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaKelly L Williams, Simon Topp, Shu Yang, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Genome Biology|March 27, 2021
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disordersMarta F Nabais, Simon M Laws, Tian Lin, et al.
Pageof 40

Showing results (381-390 of 396) with videos related to

Sort By:
Pageof 40
BMJ Open|June 18, 2026
Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profileAnjali K Henders, Laura Ziser, Fleur C Garton, et al.
Brain : a Journal of Neurology|March 19, 2020
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosisCarol Dobson-Stone, Marianne Hallupp, Hamideh Shahheydari, et al.
Ophthalmology|May 26, 2016
Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter StudyYoshihiro Yonekawa, Wei-Chi Wu, Shunji Kusaka, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2011
A yeast functional screen predicts new candidate ALS disease genesJulien Couthouis, Michael P Hart, James Shorter, et al.
Ophthalmology. Retina|November 29, 2024
Clinical Characteristics and Treatment Outcomes in Unilateral Coats Disease: A Global Collaborative StudyAndrew S H Tsai, Chung-Ting Wang, Thomas C Lee, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|September 22, 2017
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBeben Benyamin, Ji He, Qiongyi Zhao, et al.
Nature Communications|April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaKelly L Williams, Simon Topp, Shu Yang, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Genome Biology|March 27, 2021
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disordersMarta F Nabais, Simon M Laws, Tian Lin, et al.
Pageof 40