Lista de obras - Richard Wooster - Dominio Público Uruguay

A census of human cancer genes

artículo científico publicado en 2004

A genome wide linkage search for breast cancer susceptibility genes

artículo científico publicado en 2006

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome

artículo científico publicado en 1992

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

artículo científico publicado en 2006

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

artículo científico publicado en 2005

A survey of RNA editing in human brain

artículo científico publicado en 2004

A survey of homozygous deletions in human cancer genomes

artículo científico publicado en 2005

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

artículo científico publicado en 2009

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer

artículo científico publicado en 1993

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers ⬇️

artículo científico publicado el 1 de enero de 1997

Amplification and overexpression of E2F3 in human bladder cancer

artículo científico publicado en 2004

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

artículo científico publicado en 2007

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

artículo científico publicado en 2007

BRCA2 mutations in primary breast and ovarian cancers

artículo científico publicado en 1996

Breast and ovarian cancer

artículo científico publicado en 2003

COSMIC 2005

artículo científico publicado en 2006

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13 ⬇️

artículo científico publicado el 1 de julio de 1997

Cancer and genomics

artículo científico publicado en 2001

Catalogue, cause, complexity and cure; the many uses of cancer genome sequence

scientific article published on 09 April 2010

Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene

artículo científico publicado en 1997

Combined Phosphatase and Tensin Homolog (PTEN) Loss and Fatty Acid Synthase (FAS) Overexpression Worsens the Prognosis of Chinese Patients with Hepatocellular Carcinoma ⬇️

artículo científico publicado el 10 de agosto de 2012

Comprehensive Predictive Biomarker Analysis for MEK Inhibitor GSK1120212 ⬇️

artículo científico publicado el 14 de diciembre de 2011

Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.

artículo científico publicado en 1995

Erratum to: Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer

artículo científico publicado en 2017

Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

scholarly article published in Nature Genetics

Erratum: Identification of the breast cancer susceptibility gene BRCA2

artículo científico publicado en 1996

Erratum: The DNA sequence and biological annotation of human chromosome

scientific article published in Nature

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene

artículo científico publicado en 1995

Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.

artículo científico publicado en 1994

Gene expression profiling after radiation-induced DNA damage is strongly predictive of BRCA1 mutation carrier status

artículo científico publicado en 2004

Genome-wide DNA copy number predictors of lapatinib sensitivity in tumor-derived cell lines

artículo científico publicado en 2008

Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays

artículo científico publicado en 2003

Hereditary predisposition to breast cancer

artículo científico publicado en 1996

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients ⬇️

artículo científico publicado el 1 de octubre de 1998

High chromosome number in hematological cancer cell lines is a negative predictor of response to the inhibition of Aurora B and C by GSK1070916.

artículo científico publicado en 2011

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison

artículo científico publicado en 2006

High-content analysis of cancer genome DNA alterations

scientific article published on February 2008

High-resolution analysis of DNA copy number using oligonucleotide microarrays

artículo científico publicado en 2004

Identification of amplified and expressed genes in breast cancer by comparative hybridization onto microarrays of randomly selected cDNA clones

artículo científico publicado en 2002

Identification of the breast cancer susceptibility gene BRCA2

artículo científico publicado en 1995

Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases

artículo científico publicado en 2009

Instability of short tandem repeats (microsatellites) in human cancers.

artículo científico publicado en 1994

Kaposi's sarcoma-associated herpesvirus-infected primary effusion lymphoma has a plasma cell gene expression profile

artículo científico publicado en 2003

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

artículo científico publicado en 1994

Lung cancer: intragenic ERBB2 kinase mutations in tumours

artículo científico publicado en 2004

Mitogen-activated protein kinase (MEK/ERK) inhibition sensitizes cancer cells to centromere-associated protein E inhibition

artículo científico publicado en 2012

Molecular target class is predictive of in vitro response profile

artículo científico publicado en 2010

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

artículo científico publicado en 2006

Mutation and copy number detection in human cancers using a custom genotyping assay ⬇️

artículo científico publicado el 7 de mayo de 2011

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

artículo científico publicado en 2007

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

artículo científico publicado en 2006

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

artículo científico publicado en 2007

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

artículo científico publicado en 2007

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

artículo científico publicado en 2007

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

artículo científico publicado en 2004

Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation

artículo científico publicado en 2006

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

artículo científico publicado en 2006

Mutations of the BRAF gene in human cancer

artículo científico publicado en 2002

Patterns of somatic mutation in human cancer genomes

artículo científico publicado en 2007

Pooled shRNA screen for sensitizers to inhibition of the mitotic regulator polo-like kinase (PLK1) ⬇️

artículo científico publicado el 1 de diciembre de 2011

RNA editing of human microRNAs

artículo científico publicado en 2006

Rapid detection of DNA sequence variants by conformation-sensitive capillary electrophoresis

artículo científico publicado en 2000

Screening for ESR mutations in breast and ovarian cancer patients

artículo científico publicado en 1997

Sensitivity of cancer cells to Plk1 inhibitor GSK461364A is associated with loss of p53 function and chromosome instability

artículo científico publicado en 2010

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

artículo científico publicado en 2006

Sequence variants of the axin gene in breast, colon, and other cancers: an analysis of mutations that interfere with GSK3 binding

artículo científico publicado en 2000

Sequence-based cancer genomics: progress, lessons and opportunities

artículo científico publicado en 2003

Serial transcriptome analysis and cross-species integration identifies centromere-associated protein E as a novel neuroblastoma target

artículo científico publicado en 2010

Somatic mutations of the protein kinase gene family in human lung cancer

artículo científico publicado en 2005

Statistical analysis of pathogenicity of somatic mutations in cancer

artículo científico publicado en 2006

Systematic analysis of genotype-specific drug responses in cancer

artículo científico publicado en 2012

The BRC repeats are conserved in mammalian BRCA2 proteins

artículo científico publicado en 1997

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

artículo científico publicado en 2004

The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders

artículo científico publicado en 2005

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

artículo científico publicado en 2001

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

artículo científico publicado en 2004

Lista de obras de Richard Wooster

A census of human cancer genes

A genome wide linkage search for breast cancer susceptibility genes

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

A survey of RNA editing in human brain

A survey of homozygous deletions in human cancer genomes

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers ⬇️

Amplification and overexpression of E2F3 in human bladder cancer

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

BRCA2 mutations in primary breast and ovarian cancers

Breast and ovarian cancer

COSMIC 2005

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13 ⬇️

Cancer and genomics

Catalogue, cause, complexity and cure; the many uses of cancer genome sequence

Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene

Combined Phosphatase and Tensin Homolog (PTEN) Loss and Fatty Acid Synthase (FAS) Overexpression Worsens the Prognosis of Chinese Patients with Hepatocellular Carcinoma ⬇️

Comprehensive Predictive Biomarker Analysis for MEK Inhibitor GSK1120212 ⬇️

Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.

Erratum to: Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer

Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Erratum: Identification of the breast cancer susceptibility gene BRCA2

Erratum: The DNA sequence and biological annotation of human chromosome

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene

Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.

Gene expression profiling after radiation-induced DNA damage is strongly predictive of BRCA1 mutation carrier status

Genome-wide DNA copy number predictors of lapatinib sensitivity in tumor-derived cell lines

Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays

Hereditary predisposition to breast cancer

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients ⬇️

High chromosome number in hematological cancer cell lines is a negative predictor of response to the inhibition of Aurora B and C by GSK1070916.

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison

High-content analysis of cancer genome DNA alterations

High-resolution analysis of DNA copy number using oligonucleotide microarrays

Identification of amplified and expressed genes in breast cancer by comparative hybridization onto microarrays of randomly selected cDNA clones

Identification of the breast cancer susceptibility gene BRCA2

Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases

Instability of short tandem repeats (microsatellites) in human cancers.

Kaposi's sarcoma-associated herpesvirus-infected primary effusion lymphoma has a plasma cell gene expression profile

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

Lung cancer: intragenic ERBB2 kinase mutations in tumours

Mitogen-activated protein kinase (MEK/ERK) inhibition sensitizes cancer cells to centromere-associated protein E inhibition

Molecular target class is predictive of in vitro response profile

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

Mutation and copy number detection in human cancers using a custom genotyping assay ⬇️

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

Mutations of the BRAF gene in human cancer

Patterns of somatic mutation in human cancer genomes

Pooled shRNA screen for sensitizers to inhibition of the mitotic regulator polo-like kinase (PLK1) ⬇️

RNA editing of human microRNAs

Rapid detection of DNA sequence variants by conformation-sensitive capillary electrophoresis

Screening for ESR mutations in breast and ovarian cancer patients

Sensitivity of cancer cells to Plk1 inhibitor GSK461364A is associated with loss of p53 function and chromosome instability

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

Sequence variants of the axin gene in breast, colon, and other cancers: an analysis of mutations that interfere with GSK3 binding

Sequence-based cancer genomics: progress, lessons and opportunities

Serial transcriptome analysis and cross-species integration identifies centromere-associated protein E as a novel neuroblastoma target

Somatic mutations of the protein kinase gene family in human lung cancer

Statistical analysis of pathogenicity of somatic mutations in cancer

Systematic analysis of genotype-specific drug responses in cancer

The BRC repeats are conserved in mammalian BRCA2 proteins

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

Whole genome DNA copy number changes identified by high density oligonucleotide arrays