Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient

[1]  K. Kinzler,et al.  Cancer Genome Landscapes , 2013, Science.

[2]  Christopher A. Miller,et al.  Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma , 2013, Genome research.

[3]  C. Swanton,et al.  The centriolar satellite protein Cep131 is important for genome stability , 2013, Development.

[4]  Helga Thorvaldsdóttir,et al.  Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration , 2012, Briefings Bioinform..

[5]  C. Swanton,et al.  The centriolar satellite protein Cep131 is important for genome stability , 2012, Journal of Cell Science.

[6]  R. Friedrich,et al.  Vascular wall cells contribute to tumourigenesis in cutaneous neurofibromas of patients with neurofibromatosis type 1. A comparative histological, ultrastructural and immunohistochemical study. , 2012, Anticancer research.

[7]  D. Cooper,et al.  Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas , 2011, European Journal of Human Genetics.

[8]  D. Cooper,et al.  Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis , 2011, Human Genomics.

[9]  Helga Thorvaldsdóttir,et al.  Integrative Genomics Viewer , 2011, Nature Biotechnology.

[10]  Jana Marie Schwarz,et al.  MutationTaster evaluates disease-causing potential of sequence alterations , 2010, Nature Methods.

[11]  D. Horn,et al.  Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family , 2010, BMC Medical Genetics.

[12]  H. Hakonarson,et al.  ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.

[13]  Richard Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[14]  D. Burns,et al.  Cell of origin and microenvironment contribution for NF1-associated dermal neurofibromas. , 2009, Cell stem cell.

[15]  R. Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[16]  N. Ratner,et al.  How does the Schwann cell lineage form tumors in NF1? , 2008, Glia.

[17]  M. Wallace,et al.  Influence of hormones and hormone metabolites on the growth of schwann cells derived from embryonic stem cells and on tumor cell lines expressing variable levels of neurofibromin , 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

[18]  F. Speleman,et al.  Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1. , 2007, American journal of human genetics.

[19]  D. Gutmann,et al.  Optic nerve glioma in mice requires astrocyte Nf1 gene inactivation and Nf1 brain heterozygosity. , 2003, Cancer research.

[20]  D. Gutmann,et al.  Astrocyte-Specific Inactivation of the Neurofibromatosis 1 Gene (NF1) Is Insufficient for Astrocytoma Formation , 2002, Molecular and Cellular Biology.

[21]  D. Gutmann,et al.  International consensus statement on malignant peripheral nerve sheath tumors in neurofibromatosis. , 2002, Cancer research.