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Lista de obras de David Vetrie

A Complete YAC Contig and Cosmid Interval Map Covering the Entirety of Human Xq21.33 to Xq22.3 from DXS3 to DXS287

scientific article published on 01 July 1997

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness

artículo científico publicado en 1996

Applications of genomic microarrays to explore human chromosome structure and function.

artículo científico publicado en 2004

Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16

artículo científico publicado en 2008

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays

artículo científico publicado en 2005

CML cells actively evade host immune surveillance through cytokine-mediated downregulation of MHC-II expression.

artículo científico publicado en 2016

Cancer: Repositioned to kill stem cells

artículo científico publicado en 2015

Characterization of DRP2, a novel human dystrophin homologue

scientific journal article

Chromatin looping defines expression of TAL1, its flanking genes, and regulation in T-ALL.

artículo científico publicado en 2013

Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution

artículo científico publicado en 2010

Construction of a yeast artificial chromosome contig encompassing the human alpha 5(IV) collagen gene (COL4A5).

artículo científico publicado en 1992

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

artículo científico publicado en 2003

DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis

article

Detection of mutations in COL4A5 in patients with Alport Syndrome

article

Dual targeting of p53 and c-MYC selectively eliminates leukaemic stem cells

artículo científico publicado en 2016

Epigenetic Reprogramming Sensitizes CML Stem Cells to Combined EZH2 and Tyrosine Kinase Inhibition

artículo científico publicado en 2016

Epigenetic dysregulation in chronic myeloid leukaemia: A myriad of mechanisms and therapeutic options.

artículo científico publicado en 2017

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome

artículo científico publicado en 2005

Expression profiling of the Leishmania life cycle: cDNA arrays identify developmentally regulated genes present but not annotated in the genome

artículo científico publicado en 2004

From genomes to vaccines: Leishmania as a model

artículo científico publicado en 2002

Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level

artículo científico publicado en 2009

Gene expression profiling in polycythemia vera using cDNA microarray technology.

artículo científico publicado en 2003

Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology

article

Genetic aspects of renal dysfunction: Alport's syndrome

artículo científico publicado en 1994

Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus

artículo científico publicado en 2010

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

artículo científico publicado en 2007

Identification of Btk mutations in 20 unrelated patients with X-Iinked agammaglobulinaemia (XLA)

article

Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia

artículo científico publicado en 1994

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.

artículo científico publicado en 2005

Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites

artículo científico publicado en 2006

Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.

artículo científico publicado en 1993

Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22

artículo científico publicado en 1994

Long-range mapping of the gene for the human alpha 5(IV) collagen chain at Xq22-q23.

artículo científico publicado en 1992

Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome

article

Molecular diagnosis of X-linked agammaglobulinaemia

artículo científico publicado en 1993

Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH.

artículo científico publicado en 1998

Physical mapping shows close linkage between the alpha-galactosidase A gene (GLA) and the DXS178 locus.

artículo científico publicado en 1993

Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms

artículo científico publicado en 2004

Requirement of bic/microRNA-155 for normal immune function

artículo científico publicado en 2007

Somatic mosaicism associated with a mild Alport syndrome phenotype

artículo científico publicado en 2000

Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease

artículo científico publicado en 1994

The chronic myeloid leukemia stem cell: stemming the tide of persistence

artículo científico publicado en 2017

The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993.

artículo científico publicado en 2012

The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins

artículo científico publicado en 1999

The implications of the cloning of the XLA gene.

artículo científico publicado en 1993

The landscape of histone modifications across 1% of the human genome in five human cell lines

artículo científico publicado en 2007

The leukaemia stem cell: similarities, differences and clinical prospects in CML and AML

scientific article published on 06 January 2020

Tyrosine kinase inhibitor independent gene expression signature in CML offers new targets for LSPC eradication therapy

Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data

artículo científico publicado en 2003

X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease

artículo científico publicado el 1 de septiembre de 1992

X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?

artículo científico publicado en 1992