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Germline TP53 mutations and Li-Fraumeni syndrome

Human mutation, 2003-03, Vol.21 (3), p.313-320

Varley, J.M.

2003

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Li-Fraumeni syndrome - a molecular and clinical review

British journal of cancer, 1997-07, Vol.76 (1), p.1-14

1997

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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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Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation

Journal of medical genetics, 2003-11, Vol.40 (11), p.802-806

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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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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Characterization of germline TP53 splicing mutations and their genetic and functional analysis

Oncogene, 2001-05, Vol.20 (21), p.2647-2654

2001

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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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Low rate of TP53 germline mutations in breast cancer/sarcoma families not fulfilling classical criteria for Li-Fraumeni syndrome

Journal of medical genetics, 2002-12, Vol.39 (12), p.941-944

2002

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A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene

Oncogene, 1997-02, Vol.14 (7), p.865-871

1997

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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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Comparative genomic hybridisation of ductal carcinoma in situ of the breast : identification of regions of DNA amplification and deletion in common with invasive breast carcinoma

Oncogene, 1997-03, Vol.14 (9), p.1059-1065

1997

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Two functional assays employed to detect an unusual mutation in the oligomerisation domain of p53 in a Li-Fraumeni like family

Oncogene, 1997-04, Vol.14 (15), p.1869-1874

1997

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Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy

British journal of cancer, 1997, Vol.76 (12), p.1546-1549

1997

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Frequent alterations of cell cycle regulators in early-stage breast lesions as detected by immunohistochemistry

British journal of cancer, 1998-05, Vol.77 (9), p.1460-1468

1998

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Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization

British Journal of Cancer, 1999-09, Vol.81 (2), p.300-304

1999

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Genetic and functional studies of a germline TP53 splicing mutation in a Li - Fraumeni-like family

Oncogene, 1998-06, Vol.16 (25), p.3291-3298

1998

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Delayed Chromosome Changes in Gamma-Irradiated Normal and Li-Fraumeni Fibroblasts

Radiation research, 2002-02, Vol.157 (2), p.158-165

2002

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Somatic glypican 3 ( ) mutations in Wilms' tumour

British journal of cancer, 2002-06, Vol.86 (12), p.1920-1922

2002

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Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni families

British journal of cancer, 1998-06, Vol.77 (12), p.2181-2192

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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Immunohistochemical analysis of expression and allelotype of mismatch repair genes ( and ) in bladder cancer

British journal of cancer, 2001-02, Vol.84 (3), p.321-328

2001

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An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53

Journal of medical genetics, 1995-12, Vol.32 (12), p.942-945

1995

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The relationship between radiation-induced G1 arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations

British journal of cancer, 2001-07, Vol.85 (2), p.293-296

2001

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Genomic alterations associated with loss of heterozygosity for TP53 in Li-Fraumeni syndrome fibroblasts

British journal of cancer, 2000-08, Vol.83 (4), p.467-472

2000

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Germline TP53 mutations and Li-Fraumeni syndrome

Li-Fraumeni syndrome - a molecular and clinical review

Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation

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

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

Characterization of germline TP53 splicing mutations and their genetic and functional analysis

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

Low rate of TP53 germline mutations in breast cancer/sarcoma families not fulfilling classical criteria for Li-Fraumeni syndrome

A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene

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

Comparative genomic hybridisation of ductal carcinoma in situ of the breast : identification of regions of DNA amplification and deletion in common with invasive breast carcinoma

Two functional assays employed to detect an unusual mutation in the oligomerisation domain of p53 in a Li-Fraumeni like family

Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy

Frequent alterations of cell cycle regulators in early-stage breast lesions as detected by immunohistochemistry

Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization

Genetic and functional studies of a germline TP53 splicing mutation in a Li - Fraumeni-like family

Delayed Chromosome Changes in Gamma-Irradiated Normal and Li-Fraumeni Fibroblasts

Somatic glypican 3 ( ) mutations in Wilms' tumour

Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni families

Structural Rearrangement of the Retinoblastoma Gene in Human Breast Carcinoma

Immunohistochemical analysis of expression and allelotype of mismatch repair genes ( and ) in bladder cancer

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53

The relationship between radiation-induced G1 arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations

Genomic alterations associated with loss of heterozygosity for TP53 in Li-Fraumeni syndrome fibroblasts

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