Denise Sheer


Ontology type: schema:Person     


Person Info

NAME

Denise

SURNAME

Sheer

Publications in SciGraph latest 50 shown

  • 2016-12 DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2016-11 Genome-wide methylation analysis identifies genes silenced in non-seminoma cell lines in NPJ GENOMIC MEDICINE
  • 2015-12 Molecular analysis of pediatric brain tumors identifies microRNAs in pilocytic astrocytomas that target the MAPK and NF-κB pathways in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2013-12 BORIS/CTCFL is an RNA-binding protein that associates with polysomes in BMC CELL BIOLOGY
  • 2013-06 Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas in NATURE GENETICS
  • 2013-04 Three different brain tumours evolving from a common origin in ONCOGENESIS
  • 2010-12 MYB upregulation and genetic aberrations in a subset of pediatric low-grade gliomas in ACTA NEUROPATHOLOGICA
  • 2010-08 RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort in ACTA NEUROPATHOLOGICA
  • 2010-07 Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome in NATURE
  • 2010-06 Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome in NATURE
  • 2008-12 Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis in BMC MEDICAL GENOMICS
  • 2008-09 Anchoring the genome in GENOME BIOLOGY
  • 2007-07 A role for SC35 and hnRNPA1 in the determination of amyloid precursor protein isoforms in MOLECULAR PSYCHIATRY
  • 2006 Nuclear Compartments in ENCYCLOPEDIC REFERENCE OF GENOMICS AND PROTEOMICS IN MOLECULAR MEDICINE
  • 2002-04 HnRNP-A1 binds directly to double-stranded DNA in vitro within a 36 bp sequence in MOLECULAR AND CELLULAR BIOCHEMISTRY
  • 2001-08 Human Chromosomes (4th Edition) in CHROMOSOME RESEARCH
  • 2000-07 Fluorescence in situ hybridization techniques for the rapid detection of genetic prognostic factors in neuroblastoma in BRITISH JOURNAL OF CANCER
  • 1999-09 The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis in NATURE MEDICINE
  • 1999-02 Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line in BRITISH JOURNAL OF CANCER
  • 1998-02 cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases in MAMMALIAN GENOME
  • 1996-07 LIM–kinase deleted in Williams syndrome in NATURE GENETICS
  • 1996-03 H-RYK, an Unusual Receptor Kinase: Isolation and Analysis of Expression in Ovarian Cancer in MOLECULAR MEDICINE
  • 1994-08 Cloning and characterization of human phosphatase inhibitor-2 (IPP-2) sequences in MAMMALIAN GENOME
  • 1994-05 The CL100 gene, which encodes a dual specificity (Tyr/Thr) MAP kinase phosphatase, is highly conserved and maps to human chromosome 5q34 in HUMAN GENETICS
  • 1994-03 Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears in BRITISH JOURNAL OF CANCER
  • 1993-03 New vector for transfer of yeast artificial chromosomes to mammalian cells in SOMATIC CELL AND MOLECULAR GENETICS
  • 1993-01 Diagnosis of Ewing's sarcoma and peripheral neuroectodermal tumour based on the detection of t(11;22) using fluorescence in situ hybridisation in BRITISH JOURNAL OF CANCER
  • 1991-04-22 Chromosome-Mediated Gene Transfer in GENE TRANSFER AND EXPRESSION PROTOCOLS
  • 1989-12 Characterisation of human thyroid epithelial cells immortalised in vitro by simian virus 40 DNA transfection in BRITISH JOURNAL OF CANCER
  • 1989-06 The gene coding for the p68 calcium-binding protein is localised to bands q32–q34 of human chromosome 5, and to mouse chromosome 11 in HUMAN GENETICS
  • 1988-10 The human LFA-3 gene is located at the same chromosome band as the gene for its receptor CD2 in IMMUNOGENETICS
  • 1988-05 Biochemical and genetic analysis of the Oka blood group antigen in IMMUNOGENETICS
  • 1987-08 Localization of the gene for familial adenomatous polyposis on chromosome 5 in NATURE
  • 1987-07 Chromosomal locations of the gene coding for the CD3 (T3) γ subunit of the human and mouse CD3/T-cell antigen receptor complexes in IMMUNOGENETICS
  • 1987-06 The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p in HUMAN GENETICS
  • 1985-09 Transformation associated p53 protein is encoded by a gene on human chromosome 17 in SOMATIC CELL AND MOLECULAR GENETICS
  • 1985-07 Incidence of the 15q+;17q- chromosome translocation in acute promyelocytic leukaemia (APL) in BRITISH JOURNAL OF CANCER
  • 1983-03 Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome in NATURE
  • 1982-01 Carcinoembryonic antigen (CEA) expression in somatic cell hybrids in SOMATIC CELL GENETICS
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