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The FEBS Journal|March 19, 2009
Low U1 snRNP dependence at the NF1 exon 29 donor splice siteMichela Raponi, Emanuele Buratti, Elisa Dassie, et al.Human Genetics|October 11, 2011
Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?Mark Richards, Frédérique Coppée, Nick Thomas, et al.American Journal of Medical Genetics. Part A|November 4, 2004
Functional analysis of polymorphic variation within the promoter and 5' untranslated region of the neurofibromatosis type 1 (NF1) geneMartin P Horan, Michael Osborn, David N Cooper, et al.Neurogenetics|April 2, 2010
Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burdenLaura Thomas, Lan Kluwe, Nadia Chuzhanova, et al.Human Genomics|December 19, 2012
Molecular heterogeneity in malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1Laura Thomas, Victor-Felix Mautner, David N Cooper, et al.Human Genomics|December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.Human Genomics|August 17, 2013
Screening in silico predicted remotely acting NF1 gene regulatory elements for mutations in patients with neurofibromatosis type 1Stephen E Hamby, Pablo Reviriego, David N Cooper, et al.Oncotarget|April 29, 2017
Telomere erosion in NF1 tumorigenesisRhiannon E Jones, Julia W Grimstead, Ashni Sedani, et al.Pediatric Blood & Cancer|May 22, 2007
A novel mutation in the NF1 gene in two siblings with neurofibromatosis type 1 and bilateral optic pathway gliomaRejin Kebudi, Samuray Tuncer, Meena Upadhyaya, et al.Pageof 8