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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

Nature genetics, 1997-05, Vol.16 (1), p.64-67

1997

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PTEN and inherited hamartoma-cancer syndromes

Nature genetics, 1998-07, Vol.19 (3), p.223-223

1998

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Clinical and pathological features of breast disease in Cowden's syndrome: An underrecognized syndrome with an increased risk of breast cancer

Human pathology, 1998, Vol.29 (1), p.47-53

1998

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Identification of PTEN mutations in metastatic melanoma specimens

Journal of medical genetics, 2000-09, Vol.37 (9), p.653-657

2000

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Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus

Human molecular genetics, 1995-07, Vol.4 (7), p.1119-1126

1995

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Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

Journal of medical genetics, 1999-05, Vol.36 (5), p.360-364

1999

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A Biomarker that Identifies Senescent Human Cells in Culture and in Aging Skin in vivo

Proceedings of the National Academy of Sciences - PNAS, 1995-09, Vol.92 (20), p.9363-9367

1995

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Fibroblasts protect the Lyme disease spirochete, Borrelia burgdorferi, from ceftriaxone in vitro

The Journal of infectious diseases, 1992-08, Vol.166 (2), p.440-444

1992

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Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome

Human genetics, 2000-09, Vol.107 (3), p.234-238

2000

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The genetic basis of Cowden's syndrome : three novel mutations in PTEN/MMAC1/TEP1

Human genetics, 1998-04, Vol.102 (4), p.467-473

1998

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Bumps and pumps, SERCA 1999

Nature genetics, 1999-03, Vol.21 (3), p.252-253

1999

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Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5351), p.720-724

1998

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Expression of senescence-associated beta-galactosidase in enlarged prostates from men with benign prostatic hyperplasia

Urology (Ridgewood, N.J.), 2000-07, Vol.56 (1), p.160-166

2000

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Induction of Nerve Growth Factor Receptors on Cultured Human Melanocytes

Proceedings of the National Academy of Sciences - PNAS, 1988-07, Vol.85 (14), p.5282-5286

1988

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Linkage of the Wiskott--Aldrich Syndrome with Polymorphic DNA Sequences from the Human X Chromosome

Proceedings of the National Academy of Sciences - PNAS, 1987-05, Vol.84 (10), p.3430-3433

1987

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Identification of PTEN mutations in five families with Bannayan-Zonana syndrome

Experimental dermatology, 1999-04, Vol.8 (2), p.134-139

1999

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Patterns of X chromosome inactivation in sporadic basal cell carcinomas: Evidence for clonality

Journal of the American Academy of Dermatology, 1998, Vol.38 (1), p.49-55

1998

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Role of PTCH and p53 Genes in Early-Onset Basal Cell Carcinoma

The American journal of pathology, 2001-02, Vol.158 (2), p.381-385

2001

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Germline PTEN mutations in three families with Cowden syndrome

Experimental dermatology, 2000-04, Vol.9 (2), p.152-156

2000

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Antioxidant Vitamins, Cancer, and Cardiovascular Disease

The New England journal of medicine, 1996-10, Vol.335 (14), p.1065-1069

von Eggers Doering, W

1996

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PTEN/MMAC1 mutations in hepatocellular carcinomas

Oncogene, 1999-05, Vol.18 (20), p.3181-3185

1999

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Late Snow

Critical survey (Oxford, England), 1996-01, Vol.8 (3), p.323-324

PEACOCKE, M. R.

1996

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Nanny Besom

Critical survey (Oxford, England), 1996-01, Vol.8 (3), p.323-323

PEACOCKE, M. R.

1996

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Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome

Journal of the American Academy of Dermatology, 2001-02, Vol.44 (2), p.183-187

2001

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PTCH Mutations in Squamous Cell Carcinoma of the Skin

Journal of investigative dermatology, 2001-04, Vol.116 (4), p.614-616

2001

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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

PTEN and inherited hamartoma-cancer syndromes

Clinical and pathological features of breast disease in Cowden's syndrome: An underrecognized syndrome with an increased risk of breast cancer

Identification of PTEN mutations in metastatic melanoma specimens

Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus

Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

A Biomarker that Identifies Senescent Human Cells in Culture and in Aging Skin in vivo

Fibroblasts protect the Lyme disease spirochete, Borrelia burgdorferi, from ceftriaxone in vitro

Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome

The genetic basis of Cowden's syndrome : three novel mutations in PTEN/MMAC1/TEP1

Bumps and pumps, SERCA 1999

Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

Expression of senescence-associated beta-galactosidase in enlarged prostates from men with benign prostatic hyperplasia

Induction of Nerve Growth Factor Receptors on Cultured Human Melanocytes

Linkage of the Wiskott--Aldrich Syndrome with Polymorphic DNA Sequences from the Human X Chromosome

Identification of PTEN mutations in five families with Bannayan-Zonana syndrome

Patterns of X chromosome inactivation in sporadic basal cell carcinomas: Evidence for clonality

Role of PTCH and p53 Genes in Early-Onset Basal Cell Carcinoma

Germline PTEN mutations in three families with Cowden syndrome

Antioxidant Vitamins, Cancer, and Cardiovascular Disease

PTEN/MMAC1 mutations in hepatocellular carcinomas

Late Snow

Nanny Besom

Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome

PTCH Mutations in Squamous Cell Carcinoma of the Skin

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