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The Journal of Heredity|May 23, 2006
Noncanonical RNAs from transcripts of the Drosophila muscleblind geneJonathan M Houseley, Zaida Garcia-Casado, Maya Pascual, et al.Genomics|July 6, 2004
Estimating mutant microsatellite allele frequencies in somatic cells by small-pool PCRMary Coolbaugh-Murphy, Atousa Maleki, Lou Ramagli, et al.Annals of Neurology|September 27, 2002
Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1Claudia Abbruzzese, Sandro Costanzi Porrini, Bruno Mariani, et al.European Journal of Human Genetics : EJHG|July 24, 2014
Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1Fernando Morales, Melissa Vásquez, Patricia Cuenca, et al.Neuromuscular Disorders : NMD|February 6, 2021
A DM1 patient with CCG variant repeats: Reaching the diagnosisSarah A Cumming, Agata Oliwa, Gillian Stevens, et al.European Journal of Human Genetics : EJHG|November 24, 2016
Identification and characterization of 5' CCG interruptions in complex DMPK expanded allelesAnnalisa Botta, Giulia Rossi, Marzia Marcaurelio, et al.Differentiation; Research in Biological Diversity|February 21, 2007
Muscleblind isoforms are functionally distinct and regulate alpha-actinin splicingMarta Vicente, Lidón Monferrer, Michael G Poulos, et al.Human Molecular Genetics|February 11, 2005
Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to DrosophilaJonathan M Houseley, Zongsheng Wang, Graham J R Brock, et al.Neuromuscular Disorders : NMD|October 7, 2022
Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1Agata Oliwa, Clarissa Hocking, Mark J Hamilton, et al.Scientific Reports|March 2, 2021
White matter microstructure relates to motor outcomes in myotonic dystrophy type 1 independently of disease duration and genetic burdenTimothy R Koscik, Ellen van der Plas, Laurie Gutmann, et al.Pageof 10