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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Clinical cancer research, 2006-02, Vol.12 (4), p.1157-1167

2006

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Relative frequency and morphology of cancers in carriers of germline TP53 mutations

Oncogene, 2001-08, Vol.20 (34), p.4621-4628

2001

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Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Science (American Association for the Advancement of Science), 1999-12, Vol.286 (5449), p.2528-2531

1999

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Randomized, controlled trial of an intervention for toddlers with autism: the Early Start Denver Model

Pediatrics (Evanston), 2010-01, Vol.125 (1), p.e17-e23

2010

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Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Cancer research (Chicago, Ill.), 1997-08, Vol.57 (15), p.3245-3252

1997

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Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome

Oncogene, 1998-09, Vol.17 (9), p.1061-1068

1998

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Structural Rearrangement of the Retinoblastoma Gene in Human Breast Carcinoma

Science (American Association for the Advancement of Science), 1988-10, Vol.242 (4876), p.263-266

1988

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RNA polymerase III transcription can be derepressed by oncogenes or mutations that compromise p53 function in tumours and Li-Fraumeni syndrome

Oncogene, 2002-05, Vol.21 (19), p.2961-2970

2002

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Germ Line BAX Alterations Are Infrequent in Li-Fraumeni Syndrome

Cancer epidemiology, biomarkers & prevention, 2004-08, Vol.13 (8), p.1403-1406

2004

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BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

European journal of cancer (1990), 2006-05, Vol.42 (8), p.1143-1150

2006

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Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

The Lancet (British edition), 2003-03, Vol.361 (9363), p.1101-1102

2003

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Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

American journal of human genetics, 1999-10, Vol.65 (4), p.995-1006

1999

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Loss of chromosome 17p13 sequences and mutation of p53 in human breast carcinomas

Oncogene, 1991-03, Vol.6 (3), p.413-421

1991

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Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast

Oncogene, 1995-04, Vol.10 (8), p.1653-1657

1995

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Satellite DNA is transcribed on lampbrush chromosomes

Nature (London), 1980-02, Vol.283 (5748), p.686-688

1980

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Preparation, labelling and detection of DNA from archival tissue sections suitable for comparative genomic hybridization

Chromosome research, 1996-02, Vol.4 (2), p.163-164

1996

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Identification of a rare polymorphism in the human TP53 promoter

Cancer genetics and cytogenetics, 2002-06, Vol.135 (2), p.165-172

2002

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Identification and Cloning in Yeast Artificial Chromosomes of a Region of Elevated Loss of Heterozygosity on Chromosome 1p31.1 in Human Breast Cancer

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.233-243

1995

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Differential expression of the mitochondrial gene cytochrome oxidase ii in benign and malignant breast tissue

The Journal of pathology, 1992-10, Vol.168 (2), p.163-168

1992

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Transposon donor plasmids, based on ColIb-P9, for use in Pseudomonas putida and a variety of other gram negative bacteria

Molecular & general genetics, 1985-01, Vol.200 (1), p.65-67

1985

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Loss of heterozygosity on the X chromosome in human breast cancer

Genes chromosomes & cancer, 1995-08, Vol.13 (4), p.229-238

1995

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Differential expression of cellular oncogenes in benign and malignant human breast tissue

International journal of cancer, 1986-11, Vol.38 (5), p.651-655

1986

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Patterns of silver staining of human chromosomes

Chromosoma, 1977-05, Vol.61 (3), p.207-214

Varley, J M

1977

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Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qter in relation to the centromere on human chromosome 1

Chromosome research, 1995-03, Vol.3 (2), p.137-138

1995

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Confirmation of the copy number of chromosome 1 in interphase nuclei from paraffin sections of breast tumours by fluorescence in situ hybridization

Chromosome research, 1995-11, Vol.3 (7), p.410-416

1995

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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Relative frequency and morphology of cancers in carriers of germline TP53 mutations

Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Randomized, controlled trial of an intervention for toddlers with autism: the Early Start Denver Model

Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome

Structural Rearrangement of the Retinoblastoma Gene in Human Breast Carcinoma

RNA polymerase III transcription can be derepressed by oncogenes or mutations that compromise p53 function in tumours and Li-Fraumeni syndrome

Germ Line BAX Alterations Are Infrequent in Li-Fraumeni Syndrome

BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors

Loss of chromosome 17p13 sequences and mutation of p53 in human breast carcinomas

Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast

Satellite DNA is transcribed on lampbrush chromosomes

Preparation, labelling and detection of DNA from archival tissue sections suitable for comparative genomic hybridization

Identification of a rare polymorphism in the human TP53 promoter

Identification and Cloning in Yeast Artificial Chromosomes of a Region of Elevated Loss of Heterozygosity on Chromosome 1p31.1 in Human Breast Cancer

Differential expression of the mitochondrial gene cytochrome oxidase ii in benign and malignant breast tissue

Transposon donor plasmids, based on ColIb-P9, for use in Pseudomonas putida and a variety of other gram negative bacteria

Loss of heterozygosity on the X chromosome in human breast cancer

Differential expression of cellular oncogenes in benign and malignant human breast tissue

Patterns of silver staining of human chromosomes

Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qter in relation to the centromere on human chromosome 1

Confirmation of the copy number of chromosome 1 in interphase nuclei from paraffin sections of breast tumours by fluorescence in situ hybridization

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