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Neurogenetics

Showing results (811-820 of 949) with videos related to

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Neurogenetics|February 10, 2025
Identification of critical genes and drug repurposing targets in entorhinal cortex of Alzheimer's diseaseArghavan Hosseinpouri, Khadijeh Sadegh, Zeinab Zarei-Behjani, et al.
Neurogenetics|August 7, 2024
Genotypic and phenotypic analysis of Korean patients with tuberous sclerosis complexHui Jin Shin, Sangbo Lee, Se Hee Kim, et al.
Neurogenetics|August 5, 2024
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from IndiaTanushree Chawla, Saraswati Nashi, Dipti Baskar, et al.
Neurogenetics|April 8, 2006
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum proteinAshraf U Mannan, Johann Boehm, Simone M Sauter, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Neurogenetics|June 14, 2006
Investigation of autism and GABA receptor subunit genes in multiple ethnic groupsAnn L Collins, Deqiong Ma, Patrice L Whitehead, et al.
Neurogenetics|August 10, 2006
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen familiesJill Murrell, Bernardino Ghetti, Elizabeth Cochran, et al.
Neurogenetics|July 26, 2006
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplificationOronzo Scarciolla, Liborio Stuppia, Maria Vittoria De Angelis, et al.
Neurogenetics|November 11, 2006
In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndromeA G Bassuk, Y Z Chen, S D Batish, et al.
Neurogenetics|March 28, 2007
Association study of cholesterol-related genes in Alzheimer's diseaseM Axel Wollmer, Kristel Sleegers, Martin Ingelsson, et al.
Pageof 95

Showing results (811-820 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|February 10, 2025
Identification of critical genes and drug repurposing targets in entorhinal cortex of Alzheimer's diseaseArghavan Hosseinpouri, Khadijeh Sadegh, Zeinab Zarei-Behjani, et al.
Neurogenetics|August 7, 2024
Genotypic and phenotypic analysis of Korean patients with tuberous sclerosis complexHui Jin Shin, Sangbo Lee, Se Hee Kim, et al.
Neurogenetics|August 5, 2024
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from IndiaTanushree Chawla, Saraswati Nashi, Dipti Baskar, et al.
Neurogenetics|April 8, 2006
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum proteinAshraf U Mannan, Johann Boehm, Simone M Sauter, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Neurogenetics|June 14, 2006
Investigation of autism and GABA receptor subunit genes in multiple ethnic groupsAnn L Collins, Deqiong Ma, Patrice L Whitehead, et al.
Neurogenetics|August 10, 2006
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen familiesJill Murrell, Bernardino Ghetti, Elizabeth Cochran, et al.
Neurogenetics|July 26, 2006
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplificationOronzo Scarciolla, Liborio Stuppia, Maria Vittoria De Angelis, et al.
Neurogenetics|November 11, 2006
In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndromeA G Bassuk, Y Z Chen, S D Batish, et al.
Neurogenetics|March 28, 2007
Association study of cholesterol-related genes in Alzheimer's diseaseM Axel Wollmer, Kristel Sleegers, Martin Ingelsson, et al.
Pageof 95