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Hamid Hamzeiy

Showing results (11-20 of 17) with videos related to

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Bioimpacts : BI|July 11, 2023
Homozygous mutation in <i>CSF1R</i> causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS)Hossein Daghagh, Haniyeh Rahbar Kafshboran, Yousef Daneshmandpour, et al.
Neurobiology of Disease|September 7, 2016
Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levelsNesli Ece Sen, Jessica Drost, Suzana Gispert, et al.
Neuro-Degenerative Diseases|February 12, 2018
Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2Hamid Hamzeiy, Doruk Savaş, Ceren Tunca, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 2, 2018
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS casesLucia Corrado, Cinzia Tiloca, Clarissa Locci, et al.
Nature Biotechnology|July 9, 2021
MaxDIA enables library-based and library-free data-independent acquisition proteomicsPavel Sinitcyn, Hamid Hamzeiy, Favio Salinas Soto, et al.
Human Mutation|June 25, 2020
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant databaseCeren Tunca, Tuncay Şeker, Fulya Akçimen, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Bioimpacts : BI|July 11, 2023
Homozygous mutation in <i>CSF1R</i> causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS)Hossein Daghagh, Haniyeh Rahbar Kafshboran, Yousef Daneshmandpour, et al.
Neurobiology of Disease|September 7, 2016
Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levelsNesli Ece Sen, Jessica Drost, Suzana Gispert, et al.
Neuro-Degenerative Diseases|February 12, 2018
Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2Hamid Hamzeiy, Doruk Savaş, Ceren Tunca, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 2, 2018
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS casesLucia Corrado, Cinzia Tiloca, Clarissa Locci, et al.
Nature Biotechnology|July 9, 2021
MaxDIA enables library-based and library-free data-independent acquisition proteomicsPavel Sinitcyn, Hamid Hamzeiy, Favio Salinas Soto, et al.
Human Mutation|June 25, 2020
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant databaseCeren Tunca, Tuncay Şeker, Fulya Akçimen, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Pageof 2