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Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Human molecular genetics, 2000-07, Vol.9 (11), p.1651-1663

2000

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Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications

The Lancet (British edition), 1994-06, Vol.343 (8912), p.1531-1534

1994

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Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis

Science (American Association for the Advancement of Science), 1994-06, Vol.264 (5167), p.1938-1941

1994

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Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus

Human molecular genetics, 1995-03, Vol.4 (3), p.367-372

1995

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High-resolution cytogenetic-based physical map of human chromosome 16

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1178-1185

1992

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Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.169-175

1994

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Evaluation of a cosmid contig physical map of human chromosome 16

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1031-1039

1992

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A refined physical map of the long arm of human chromosome 16

Genomics (San Diego, Calif.), 1991-06, Vol.10 (2), p.308-312

1991

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Implications of FRA 16A structure for the mechanism of chromosomal fragile site genesis

Science (American Association for the Advancement of Science), 1994-06, Vol.264 (5167), p.1938-1941

1994

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Characterization of the Melanoma miRNAome by Deep Sequencing

PloS one, 2010-03, Vol.5 (3), p.e9685-e9685

2010

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Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma

PloS one, 2011-10, Vol.6 (10), p.e26121-e26121

2011

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Whole genome expression array profiling highlights differences in mucosal defense genes in Barrett's esophagus and esophageal adenocarcinoma

PloS one, 2011-07, Vol.6 (7), p.e22513-e22513

2011

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Similarity of aberrant DNA methylation in Barrett's esophagus and esophageal adenocarcinoma

Molecular cancer, 2008-10, Vol.7 (1), p.75-75, Article 75

2008

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Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis

Nature communications, 2014-10, Vol.5 (1), p.5224-5224, Article 5224

2014

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Identification of the CIMP-like subtype and aberrant methylation of members of the chromosomal segregation and spindle assembly pathways in esophageal adenocarcinoma

Carcinogenesis (New York), 2016-04, Vol.37 (4), p.356-365

2016

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Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

Nature genetics, 1997-10, Vol.17 (2), p.198-200

1997

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Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays

Cancer research (Chicago, Ill.), 2008-06, Vol.68 (11), p.4163-4172

2008

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High-Risk Human Papillomavirus in Esophageal Squamous Cell Carcinoma

Cancer epidemiology, biomarkers & prevention, 2010-08, Vol.19 (8), p.2080-2087

2010

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Genome Scan of Schizophrenia

The American journal of psychiatry, 1998-06, Vol.155 (6), p.741-750

1998

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Endometriosis and the Fallopian Tubes: Theories of Origin and Clinical Implications

Journal of clinical medicine, 2020-06, Vol.9 (6), p.1905

2020

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Positron Emission Tomography 18F-Fluorodeoxyglucose Uptake Correlates with KRAS and EMT Gene Signatures in Operable Esophageal Adenocarcinoma

The Journal of surgical research, 2018-12, Vol.232, p.621-628

2018

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Implantation in the lower half of the uterine cavity and decreased trophoblastic thickness can predict subsequent miscarriage: a prospective cohort study

Reproduction & fertility, 2023-10, Vol.4 (4), p.1-7

2023

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National Survey Highlights the Urgent Need for Standardisation of Embryo Transfer Techniques in the UK

Journal of clinical medicine, 2021-06, Vol.10 (13), p.2839

2021

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SiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip data

PloS one, 2007-10, Vol.2 (10), p.e1093

2007

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UBCH5 Family Members Differentially Impact Stabilization of Mutant p53 via RNF128 Iso1 During Barrett’s Progression to Esophageal Adenocarcinoma

Cellular and molecular gastroenterology and hepatology, 2022-01, Vol.13 (1), p.129-149

2022

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Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications

Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis

Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus

High-resolution cytogenetic-based physical map of human chromosome 16

Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

Evaluation of a cosmid contig physical map of human chromosome 16

A refined physical map of the long arm of human chromosome 16

Implications of FRA 16A structure for the mechanism of chromosomal fragile site genesis

Characterization of the Melanoma miRNAome by Deep Sequencing

Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma

Whole genome expression array profiling highlights differences in mucosal defense genes in Barrett's esophagus and esophageal adenocarcinoma

Similarity of aberrant DNA methylation in Barrett's esophagus and esophageal adenocarcinoma

Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis

Identification of the CIMP-like subtype and aberrant methylation of members of the chromosomal segregation and spindle assembly pathways in esophageal adenocarcinoma

Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays

High-Risk Human Papillomavirus in Esophageal Squamous Cell Carcinoma

Genome Scan of Schizophrenia

Endometriosis and the Fallopian Tubes: Theories of Origin and Clinical Implications

Positron Emission Tomography 18F-Fluorodeoxyglucose Uptake Correlates with KRAS and EMT Gene Signatures in Operable Esophageal Adenocarcinoma

Implantation in the lower half of the uterine cavity and decreased trophoblastic thickness can predict subsequent miscarriage: a prospective cohort study

National Survey Highlights the Urgent Need for Standardisation of Embryo Transfer Techniques in the UK

SiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip data

UBCH5 Family Members Differentially Impact Stabilization of Mutant p53 via RNF128 Iso1 During Barrett’s Progression to Esophageal Adenocarcinoma

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