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Neurogenetics

Showing results (421-430 of 1,081) with videos related to

Pageof 109
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Neurogenetics|November 1, 2025
Differential genetic background control state-dependent courtship ultrasonic vocalizations in miceSaeyeon Na, Jia Ryoo, Chang Bum Ko, et al.
Neurogenetics|September 24, 2025
A novel hybrid deep learning model for segmentation and uzzy Res-LeNet based classification for Alzheimer's diseaseSoujanya R, Syamala Maganti, Sai Hanuman Akundi
Neurogenetics|August 11, 2025
First clinical diagnosis of FAME3 via commercial Long-Read sequencing reveals mosaic repeat expansion in MARCHF6 geneB Lakshitha A Perera, Russell Stewart, Yutaka Furuta, et al.
Neurogenetics|September 19, 2025
Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource settingAndika Priamas Nugrahanto, Agung Triono, Neti Nurani, et al.
Neurogenetics|July 29, 2025
Pro-inflammatory cytokine genetic variants show variable susceptibility to mild cognitive impairment, alzheimer's disease and frontotemporal dementia in South IndiaAswathy Peethambaran Mallika, Jairani Pushparajan Sulajamani, Mathuranath Pavagada Sivasankara, et al.
Neurogenetics|March 26, 2025
Mitochondrial DNA variants revealed by whole exome sequencing: from screening to diagnosis and follow-upSebastian Skoczylas, Tomasz Płoszaj, Karolina Gadzalska, et al.
Neurogenetics|January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosisDennis Lal, Kerstin Becker, Susanne Motameny, et al.
Neurogenetics|March 5, 2013
Dysregulation of FHL1 spliceforms due to an indel mutation produces an Emery-Dreifuss muscular dystrophy plus phenotypeHeather R Tiffin, Zandra A Jenkins, Mary J Gray, et al.
Neurogenetics|December 11, 2012
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutationsCathryn Poulton, Renske Oegema, Daphne Heijsman, et al.
Neurogenetics|January 1, 2013
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotypeCarlo C Quattrocchi, Ginevra Zanni, Antonio Napolitano, et al.
Pageof 109

Showing results (421-430 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|November 1, 2025
Differential genetic background control state-dependent courtship ultrasonic vocalizations in miceSaeyeon Na, Jia Ryoo, Chang Bum Ko, et al.
Neurogenetics|September 24, 2025
A novel hybrid deep learning model for segmentation and uzzy Res-LeNet based classification for Alzheimer's diseaseSoujanya R, Syamala Maganti, Sai Hanuman Akundi
Neurogenetics|August 11, 2025
First clinical diagnosis of FAME3 via commercial Long-Read sequencing reveals mosaic repeat expansion in MARCHF6 geneB Lakshitha A Perera, Russell Stewart, Yutaka Furuta, et al.
Neurogenetics|September 19, 2025
Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource settingAndika Priamas Nugrahanto, Agung Triono, Neti Nurani, et al.
Neurogenetics|July 29, 2025
Pro-inflammatory cytokine genetic variants show variable susceptibility to mild cognitive impairment, alzheimer's disease and frontotemporal dementia in South IndiaAswathy Peethambaran Mallika, Jairani Pushparajan Sulajamani, Mathuranath Pavagada Sivasankara, et al.
Neurogenetics|March 26, 2025
Mitochondrial DNA variants revealed by whole exome sequencing: from screening to diagnosis and follow-upSebastian Skoczylas, Tomasz Płoszaj, Karolina Gadzalska, et al.
Neurogenetics|January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosisDennis Lal, Kerstin Becker, Susanne Motameny, et al.
Neurogenetics|March 5, 2013
Dysregulation of FHL1 spliceforms due to an indel mutation produces an Emery-Dreifuss muscular dystrophy plus phenotypeHeather R Tiffin, Zandra A Jenkins, Mary J Gray, et al.
Neurogenetics|December 11, 2012
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutationsCathryn Poulton, Renske Oegema, Daphne Heijsman, et al.
Neurogenetics|January 1, 2013
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotypeCarlo C Quattrocchi, Ginevra Zanni, Antonio Napolitano, et al.
Pageof 109