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D Wöhrle

Showing results (1-10 of 32) with videos related to

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Human Genetics|August 1, 1991
Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardationD Wöhrle, P Steinbach
American Journal of Medical Genetics|August 9, 1996
DNA methylation and triplet repeat stability: new proposals addressing actual questions on the CGG repeat of fragile X syndromeD Wöhrle, S Schwemmle, P Steinbach
Chembiochem : a European Journal of Chemical Biology|February 6, 2002
Dendrimer-activated solid supports for nucleic acid and protein microarraysR Benters, C M Niemeyer, D Wöhrle
Human Genetics|October 1, 1990
Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologueD Wöhrle, J P Fryns, P Steinbach
Human Genetics|December 1, 1990
Heterozygous expression of X-linked chondrodysplasia punctata. Complex chromosome aberration including deletion of MIC2 and STSD Wöhrle, G Barbi, W Schulz, et al.
Journal of Medical Genetics|November 10, 2000
Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?U Salat, B Bardoni, D Wöhrle, et al.
Nature Genetics|June 1, 1993
Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansionD Wöhrle, I Hennig, W Vogel, et al.
Nature Genetics|January 1, 1993
A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivationK Schiebel, B Weiss, D Wöhrle, et al.
Frontiers in Neuroscience|April 23, 2024
Neuromagnetic representation of musical roundness in chord progressionsSophie D Wöhrle, Christoph Reuter, André Rupp, et al.
American Journal of Human Genetics|July 20, 2001
Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cellsD Wöhrle, U Salat, H Hameister, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Human Genetics|August 1, 1991
Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardationD Wöhrle, P Steinbach
American Journal of Medical Genetics|August 9, 1996
DNA methylation and triplet repeat stability: new proposals addressing actual questions on the CGG repeat of fragile X syndromeD Wöhrle, S Schwemmle, P Steinbach
Chembiochem : a European Journal of Chemical Biology|February 6, 2002
Dendrimer-activated solid supports for nucleic acid and protein microarraysR Benters, C M Niemeyer, D Wöhrle
Human Genetics|October 1, 1990
Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologueD Wöhrle, J P Fryns, P Steinbach
Human Genetics|December 1, 1990
Heterozygous expression of X-linked chondrodysplasia punctata. Complex chromosome aberration including deletion of MIC2 and STSD Wöhrle, G Barbi, W Schulz, et al.
Journal of Medical Genetics|November 10, 2000
Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?U Salat, B Bardoni, D Wöhrle, et al.
Nature Genetics|June 1, 1993
Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansionD Wöhrle, I Hennig, W Vogel, et al.
Nature Genetics|January 1, 1993
A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivationK Schiebel, B Weiss, D Wöhrle, et al.
Frontiers in Neuroscience|April 23, 2024
Neuromagnetic representation of musical roundness in chord progressionsSophie D Wöhrle, Christoph Reuter, André Rupp, et al.
American Journal of Human Genetics|July 20, 2001
Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cellsD Wöhrle, U Salat, H Hameister, et al.
Pageof 4