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P J Hagerman

Showing results (61-70 of 84) with videos related to

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Journal of Molecular Biology|June 9, 2001
Structural studies of the tRNA domain of tmRNAS M Stagg, A A Frazer-Abel, P J Hagerman, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Biochemistry|December 19, 1995
A noncanonical tertiary conformation of a human mitochondrial transfer RNAM A Leehey, C A Squassoni, M W Friederich, et al.
American Journal of Medical Genetics|September 20, 2000
Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNAF Tassone, R J Hagerman, D Z Loesch, et al.
Journal of Medical Genetics|April 3, 2004
Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndromeF Tassone, R J Hagerman, D Garcia-Arocena, et al.
American Journal of Human Genetics|January 13, 2000
Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndromeF Tassone, R J Hagerman, A K Taylor, et al.
Nucleic Acids Research|September 11, 1995
A nomenclature of junctions and branchpoints in nucleic acidsD M Lilley, R M Clegg, S Diekmann, et al.
Neurology|July 11, 2001
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile XR J Hagerman, M Leehey, W Heinrichs, et al.
American Journal of Medical Genetics|April 5, 2000
Clinical involvement and protein expression in individuals with the FMR1 premutationF Tassone, R J Hagerman, A K Taylor, et al.
Genes, Brain, and Behavior|December 5, 2013
Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndromeJ-C Yang, C Simon, A Schneider, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Journal of Molecular Biology|June 9, 2001
Structural studies of the tRNA domain of tmRNAS M Stagg, A A Frazer-Abel, P J Hagerman, et al.
Neuroepidemiology|February 24, 2006
Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.
Biochemistry|December 19, 1995
A noncanonical tertiary conformation of a human mitochondrial transfer RNAM A Leehey, C A Squassoni, M W Friederich, et al.
American Journal of Medical Genetics|September 20, 2000
Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNAF Tassone, R J Hagerman, D Z Loesch, et al.
Journal of Medical Genetics|April 3, 2004
Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndromeF Tassone, R J Hagerman, D Garcia-Arocena, et al.
American Journal of Human Genetics|January 13, 2000
Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndromeF Tassone, R J Hagerman, A K Taylor, et al.
Nucleic Acids Research|September 11, 1995
A nomenclature of junctions and branchpoints in nucleic acidsD M Lilley, R M Clegg, S Diekmann, et al.
Neurology|July 11, 2001
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile XR J Hagerman, M Leehey, W Heinrichs, et al.
American Journal of Medical Genetics|April 5, 2000
Clinical involvement and protein expression in individuals with the FMR1 premutationF Tassone, R J Hagerman, A K Taylor, et al.
Genes, Brain, and Behavior|December 5, 2013
Abnormal semantic processing in females with fragile X-associated tremor/ataxia syndromeJ-C Yang, C Simon, A Schneider, et al.
Pageof 9