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Neurogenetics

Showing results (671-680 of 949) with videos related to

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Neurogenetics|November 13, 2012
Splice variants of the Alzheimer's disease beta-secretase, BACE1R M Damian Holsinger, Nelleke Goense, John Bohorquez, et al.
Neurogenetics|June 15, 2014
Novel recessive myotilin mutation causes severe myofibrillar myopathyJoachim Schessl, Elisa Bach, Simone Rost, et al.
Neurogenetics|June 8, 2014
Novel compound heterozygous PIGT mutations caused multiple congenital anomalies-hypotonia-seizures syndrome 3Mitsuko Nakashima, Hirofumi Kashii, Yoshiko Murakami, et al.
Neurogenetics|June 22, 2014
A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathyAlireza Kashani, Isabelle Thiffault, Marie-Emmanuelle Dilenge, et al.
Neurogenetics|February 10, 2015
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalitiesFabian Baertling, Tobias B Haack, Richard J Rodenburg, et al.
Neurogenetics|February 28, 2015
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rateM Fittschen, I Lastres-Becker, M V Halbach, et al.
Neurogenetics|March 17, 2015
A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32Irene Sargiannidou, Gun-Ha Kim, Styliana Kyriakoudi, et al.
Neurogenetics|July 24, 2012
C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle agingOihane Jaka, Irina Kramerova, Margarita Azpitarte, et al.
Neurogenetics|August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive functionSandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Neurogenetics|August 1, 2012
Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutationShoko Tokunaga, Akihiro Hashiguchi, Akiko Yoshimura, et al.
Pageof 95

Showing results (671-680 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|November 13, 2012
Splice variants of the Alzheimer's disease beta-secretase, BACE1R M Damian Holsinger, Nelleke Goense, John Bohorquez, et al.
Neurogenetics|June 15, 2014
Novel recessive myotilin mutation causes severe myofibrillar myopathyJoachim Schessl, Elisa Bach, Simone Rost, et al.
Neurogenetics|June 8, 2014
Novel compound heterozygous PIGT mutations caused multiple congenital anomalies-hypotonia-seizures syndrome 3Mitsuko Nakashima, Hirofumi Kashii, Yoshiko Murakami, et al.
Neurogenetics|June 22, 2014
A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathyAlireza Kashani, Isabelle Thiffault, Marie-Emmanuelle Dilenge, et al.
Neurogenetics|February 10, 2015
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalitiesFabian Baertling, Tobias B Haack, Richard J Rodenburg, et al.
Neurogenetics|February 28, 2015
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rateM Fittschen, I Lastres-Becker, M V Halbach, et al.
Neurogenetics|March 17, 2015
A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32Irene Sargiannidou, Gun-Ha Kim, Styliana Kyriakoudi, et al.
Neurogenetics|July 24, 2012
C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle agingOihane Jaka, Irina Kramerova, Margarita Azpitarte, et al.
Neurogenetics|August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive functionSandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Neurogenetics|August 1, 2012
Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutationShoko Tokunaga, Akihiro Hashiguchi, Akiko Yoshimura, et al.
Pageof 95