David E Housman


Ontology type: schema:Person     


Person Info

NAME

David E

SURNAME

Housman

Publications in SciGraph latest 50 shown

  • 2017-12 HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse models in SCIENTIFIC REPORTS
  • 2017-05 Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice in NATURE NEUROSCIENCE
  • 2012-06 Acquired MET expression confers resistance to EGFR inhibition in a mouse model of glioblastoma multiforme in ONCOGENE
  • 2010-10 Rapid haplotype inference for nuclear families in GENOME BIOLOGY
  • 2009-10 Association between arterial stiffness and variations in oestrogen-related genes in JOURNAL OF HUMAN HYPERTENSION
  • 2008-07 The protective effect of KCNMB1 E65K against hypertension is restricted to blood pressure treatment with β-blockade in JOURNAL OF HUMAN HYPERTENSION
  • 2006-06 Huntington's Disease: A transcriptional report card from the peripheral blood: Can it measure disease progression in Huntington's disease? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2005-08 Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor in NATURE GENETICS
  • 2004-10 Erratum: CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation in NATURE MEDICINE
  • 2004-09 CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation in NATURE MEDICINE
  • 2004-02 Identification of an angiogenic factor that when mutated causes susceptibility to Klippel–Trenaunay syndrome in NATURE
  • 2003-05 Killing cancer by targeting genes that cancer cells have lost: Allele-specific inhibition, a novel approach to the treatment of genetic disorders in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2002-04 A bivalent Huntingtin binding peptide suppresses polyglutamine aggregation and pathogenesis in Drosophila in NATURE GENETICS
  • 2001-10 Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila in NATURE
  • 2000-11 Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes in MOLECULAR PSYCHIATRY
  • 2000-07 Direct haplotyping of kilobase-size DNA using carbon nanotube probes in NATURE BIOTECHNOLOGY
  • 1998-12 Isolation of 48 genetic markers appropriate for high throughput genotyping of inbred rat strains by B1 repetitive sequence-representational difference analysis in MAMMALIAN GENOME
  • 1998-03 Cloning and chromosomal mapping of an orphan chemokine receptor: mouse RDC1 in IMMUNOGENETICS
  • 1998-01 Characterization of an abundant short interspersed nuclear element (SINE) present in Canis familiaris in MAMMALIAN GENOME
  • 1996-09 The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein in NATURE GENETICS
  • 1996-07 Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy in NATURE GENETICS
  • 1996-05 Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning in MAMMALIAN GENOME
  • 1996-04 Genetic mapping of a pulmonary adenoma resistance locus (Par1) in mouse in NATURE GENETICS
  • 1996-02 The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9 in NATURE GENETICS
  • 1996-01 Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours in NATURE
  • 1996 The Molecular Genetics of Wilms Tumor in CANCER GENES
  • 1995-11 Schizophrenia susceptibility and chromosome 6p24–22 in NATURE GENETICS
  • 1994-10 Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): Generation of a 5-cM, >5 megabase contig on mouse Chromosome 1 in MAMMALIAN GENOME
  • 1994-01 Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat in SOMATIC CELL AND MOLECULAR GENETICS
  • 1993-11 Corrigendum: Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome in NATURE GENETICS
  • 1993-08 The Wilms tumour gene WT1 is expressed in murine mesoderm–derived tissues and mutated in a human mesothelioma in NATURE GENETICS
  • 1993-06 Direct detection of novel expanded trinucleotide repeats in the human genome in NATURE GENETICS
  • 1993-02 Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines in NATURE GENETICS
  • 1993-01 Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome in NATURE GENETICS
  • 1992-11 Cloning of the α–adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification in NATURE GENETICS
  • 1992-09 Mapping and characterization of 129 cosmids on human chromosome 11p in SOMATIC CELL AND MOLECULAR GENETICS
  • 1992-06 The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A in NATURE GENETICS
  • 1992-05 Generation and characterization of a human chromosome 9 cosmid library in SOMATIC CELL AND MOLECULAR GENETICS
  • 1992-05 Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome in SOMATIC CELL AND MOLECULAR GENETICS
  • 1992-05 Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development in NATURE GENETICS
  • 1992-02 Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy in NATURE
  • 1992-01 The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice in IMMUNOGENETICS
  • 1991-10 WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour in NATURE
  • 1991-09 Generation and characterization of irradiation hybrids of human chromosome 4 in SOMATIC CELL AND MOLECULAR GENETICS
  • 1991-03 Isolation and characterization of irradiation fusion hybrids from mouse Chromosome 1 for mapping Rmc-1, a gene encoding a cellular receptor for MCF class murine retroviruses in SOMATIC CELL AND MOLECULAR GENETICS
  • 1991-03 Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qter in SOMATIC CELL AND MOLECULAR GENETICS
  • 1991 Cloning and Characterization of Mouse mdr Genes in MOLECULAR AND CELLULAR BIOLOGY OF MULTIDRUG RESISTANCE IN TUMOR CELLS
  • 1990-07 The candidate Wilms' tumour gene is involved in genitourinary development in NATURE
  • 1989-11 A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids in SOMATIC CELL AND MOLECULAR GENETICS
  • 1989-11 Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish in NATURE
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