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R Krahe

Showing results (11-20 of 45) with videos related to

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Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
Gene|October 23, 1997
Expression, genomic structure and high resolution mapping to 19p13.2 of the human smooth muscle cell calponin geneJ M Miano, R Krahe, E Garcia, et al.
Human Mutation|February 5, 2000
The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. OnlineK Virtaneva, L Paulin, R Krahe, et al.
Genomics|October 10, 1995
Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23G M Hobson, R Krahe, E Garcia, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 20, 2001
Representation of acoustic communication signals by insect auditory receptor neuronsC K Machens, M B Stemmler, P Prinz, et al.
Journal of Neurology|October 1, 1996
Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?C Abbruzzese, R Krahe, M Liguori, et al.
Molecular and Cellular Probes|February 1, 1997
Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathiesL L Bachinski, A Abchee, J B Durand, et al.
American Journal of Human Genetics|May 1, 1995
De novo myotonic dystrophy mutation in a Nigerian kindredR Krahe, M Eckhart, A O Ogunniyi, et al.
Neuropathology and Applied Neurobiology|July 5, 2012
Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2A Vihola, M Sirito, L L Bachinski, et al.
Neurology|November 23, 2005
Similar brain tau pathology in DM2/PROMM and DM1/Steinert diseaseC A Maurage, B Udd, M M Ruchoux, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.
Gene|October 23, 1997
Expression, genomic structure and high resolution mapping to 19p13.2 of the human smooth muscle cell calponin geneJ M Miano, R Krahe, E Garcia, et al.
Human Mutation|February 5, 2000
The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. OnlineK Virtaneva, L Paulin, R Krahe, et al.
Genomics|October 10, 1995
Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23G M Hobson, R Krahe, E Garcia, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 20, 2001
Representation of acoustic communication signals by insect auditory receptor neuronsC K Machens, M B Stemmler, P Prinz, et al.
Journal of Neurology|October 1, 1996
Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?C Abbruzzese, R Krahe, M Liguori, et al.
Molecular and Cellular Probes|February 1, 1997
Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathiesL L Bachinski, A Abchee, J B Durand, et al.
American Journal of Human Genetics|May 1, 1995
De novo myotonic dystrophy mutation in a Nigerian kindredR Krahe, M Eckhart, A O Ogunniyi, et al.
Neuropathology and Applied Neurobiology|July 5, 2012
Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2A Vihola, M Sirito, L L Bachinski, et al.
Neurology|November 23, 2005
Similar brain tau pathology in DM2/PROMM and DM1/Steinert diseaseC A Maurage, B Udd, M M Ruchoux, et al.
Pageof 5