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Neurogenetics

Showing results (701-710 of 949) with videos related to

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Neurogenetics|November 21, 2001
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesisM A Pook, S Al-Mahdawi, C J Carroll, et al.
Neurogenetics|November 21, 2001
Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysisM Boon, I M Nolte, M Bruinenberg, et al.
Neurogenetics|May 17, 2001
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathyA Bolino, L J Lonie, M Zimmer, et al.
Neurogenetics|August 5, 2003
Dementia with Lewy bodies: disease concept and geneticsManuel B Graeber, Ulrich Müller
Neurogenetics|February 20, 2019
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypesEwelina Elert-Dobkowska, Iwona Stepniak, Wioletta Krysa, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Neurogenetics|January 4, 2022
Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular centerKun Huang, Qiu-Xiang Li, Hui-Qian Duan, et al.
Neurogenetics|May 7, 2008
Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb regionMegan Brewer, Febriani Changi, Anthony Antonellis, et al.
Neurogenetics|March 19, 2008
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutationAna B Rodríguez-Martínez, Miguel A Alfonso-Sánchez, José A Peña, et al.
Neurogenetics|January 19, 2012
Distinct DNA binding and transcriptional repression characteristics related to different ARX mutationsGinam Cho, MacLean P Nasrallah, Youngshin Lim, et al.
Pageof 95

Showing results (701-710 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|November 21, 2001
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesisM A Pook, S Al-Mahdawi, C J Carroll, et al.
Neurogenetics|November 21, 2001
Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysisM Boon, I M Nolte, M Bruinenberg, et al.
Neurogenetics|May 17, 2001
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathyA Bolino, L J Lonie, M Zimmer, et al.
Neurogenetics|August 5, 2003
Dementia with Lewy bodies: disease concept and geneticsManuel B Graeber, Ulrich Müller
Neurogenetics|February 20, 2019
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypesEwelina Elert-Dobkowska, Iwona Stepniak, Wioletta Krysa, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Neurogenetics|January 4, 2022
Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular centerKun Huang, Qiu-Xiang Li, Hui-Qian Duan, et al.
Neurogenetics|May 7, 2008
Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb regionMegan Brewer, Febriani Changi, Anthony Antonellis, et al.
Neurogenetics|March 19, 2008
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutationAna B Rodríguez-Martínez, Miguel A Alfonso-Sánchez, José A Peña, et al.
Neurogenetics|January 19, 2012
Distinct DNA binding and transcriptional repression characteristics related to different ARX mutationsGinam Cho, MacLean P Nasrallah, Youngshin Lim, et al.
Pageof 95