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J C Jen

Showing results (1-10 of 21) with videos related to

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Proceedings of the National Science Council, Republic of China. Part B, Life Sciences|January 1, 1993
Complete nucleotide sequence and identification of a putative promoter region for the expression in Escherichia coli of the cryIA(b) gene from Bacillus thuringiensis var. aizawai HD133K F Chak, J C Jen
Annals of the New York Academy of Sciences|November 17, 2001
Similar oculomotor phenotypes in episodic ataxia type 2 and spinocerebellar atrophy type 6S H Ying, J C Jen, R W Baloh
American Journal of Human Genetics|November 5, 1997
Progressive ataxia due to a missense mutation in a calcium-channel geneQ Yue, J C Jen, S F Nelson, et al.
Annals of Neurology|June 21, 2001
Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7A K Oh, K M Jacobson, J C Jen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 1998
Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxiaJ C Jen, Q Yue, J Karrim, et al.
Neuroscience|July 17, 1999
Differential subcellular immunolocalization of voltage-gated calcium channel alpha1 subunits in the chinchilla cristae ampullarisI López, G Ishiyama, A Ishiyama, et al.
American Journal of Medical Genetics|May 26, 1998
De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxiaQ Yue, J C Jen, M M Thwe, et al.
Neurology|November 15, 2006
Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxiaJ C Jen, H Lee, Y H Cha, et al.
American Journal of Medical Genetics|September 19, 1998
Familial migraine with vertigo: no mutations found in CACNA1AJ S Kim, Q Yue, J C Jen, et al.
Neurology|August 24, 2005
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizuresJ C Jen, J Wan, T P Palos, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Proceedings of the National Science Council, Republic of China. Part B, Life Sciences|January 1, 1993
Complete nucleotide sequence and identification of a putative promoter region for the expression in Escherichia coli of the cryIA(b) gene from Bacillus thuringiensis var. aizawai HD133K F Chak, J C Jen
Annals of the New York Academy of Sciences|November 17, 2001
Similar oculomotor phenotypes in episodic ataxia type 2 and spinocerebellar atrophy type 6S H Ying, J C Jen, R W Baloh
American Journal of Human Genetics|November 5, 1997
Progressive ataxia due to a missense mutation in a calcium-channel geneQ Yue, J C Jen, S F Nelson, et al.
Annals of Neurology|June 21, 2001
Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7A K Oh, K M Jacobson, J C Jen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 1998
Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxiaJ C Jen, Q Yue, J Karrim, et al.
Neuroscience|July 17, 1999
Differential subcellular immunolocalization of voltage-gated calcium channel alpha1 subunits in the chinchilla cristae ampullarisI López, G Ishiyama, A Ishiyama, et al.
American Journal of Medical Genetics|May 26, 1998
De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxiaQ Yue, J C Jen, M M Thwe, et al.
Neurology|November 15, 2006
Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxiaJ C Jen, H Lee, Y H Cha, et al.
American Journal of Medical Genetics|September 19, 1998
Familial migraine with vertigo: no mutations found in CACNA1AJ S Kim, Q Yue, J C Jen, et al.
Neurology|August 24, 2005
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizuresJ C Jen, J Wan, T P Palos, et al.
Pageof 3