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Human cutaneous melanoma; a review of NRAS and BRAF mutation frequencies in relation to histogenetic subclass and body site

Molecular oncology, 2008-04, Vol.1 (4), p.395-405

2008

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NRAS and BRAF Mutations Arise Early during Melanoma Pathogenesis and Are Preserved throughout Tumor Progression

Clinical cancer research, 2003-12, Vol.9 (17), p.6483-6488

2003

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N-ras Mutations are Common in Melanomas from Sun-Exposed Skin of Humans but Rare in Mucosal Membranes or Unexposed Skin

Journal of investigative dermatology, 1998-11, Vol.111 (5), p.757-761

1998

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Biallelic Deletions in INK4 in Cutaneous Melanoma Are Common and Associated with Decreased Survival

Clinical cancer research, 2005-04, Vol.11 (8), p.2991-2997

2005

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NRAS and BRAF mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing

Melanoma research, 2006-12, Vol.16 (6), p.471-478

2006

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Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma

JNCI : Journal of the National Cancer Institute, 2002-06, Vol.94 (12), p.894-903

2002

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Cytoplasmic and nuclear accumulation of ?-catenin is rarely caused byCTNNB1 exon 3 mutations in cutaneous malignant melanoma

International journal of cancer, 2001-06, Vol.92 (6), p.839-842

2001

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Screening of N-ras codon 61 Mutations in paired primary and metastatic cutaneous melanomas: Mutations occur early and persist throughout tumor progression

Clinical cancer research, 2002-11, Vol.8 (11), p.3468-3474

2002

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Cytoplasmic and nuclear accumulation of β‐catenin is rarely caused by CTNNB1 exon 3 mutations in cutaneous malignant melanoma

International journal of cancer, 2001-06, Vol.92 (6), p.839-842

2001

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Frequency of UV-Inducible NRAS Mutations in Melanomas of Patients With Germline CDKN2A Mutations

JNCI : Journal of the National Cancer Institute, 2003-06, Vol.95 (11), p.790-798

2003

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CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas

Cancer research (Chicago, Ill.), 2000-12, Vol.60 (24), p.6864-6867

2000

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Pyrosequencing as an Alternative to Single-Strand Conformation Polymorphism Analysis for Detection of N-ras Mutations in Human Melanoma Metastases

Clinical chemistry (Baltimore, Md.), 2002-12, Vol.48 (12), p.2164-2170

2002

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Hereditary cutaneous melanoma

Seminars in cancer biology, 2000-08, Vol.10 (4), p.319-326

2000

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Screening of Germline Mutations in the CDKN2A and CDKN2B Genes in Swedish Families With Hereditary Cutaneous Melanoma

JNCI : Journal of the National Cancer Institute, 1997-05, Vol.89 (10), p.697-702

1997

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Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patients

Human pathology, 2004, Vol.35 (1), p.25-33

2004

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Germline CDKN2A mutations are rare in child and adolescent cutaneous melanoma

Melanoma research, 2004-08, Vol.14 (4), p.251-255

2004

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p53 protein expression and TP53 mutations in malignant melanomas of sun-sheltered mucosal membranes versus chronically sun-exposed skin

Melanoma research, 2004-10, Vol.14 (5), p.395-401

2004

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P-03 CCND1 A870G polymorphism and age of onset of melanoma

Melanoma research, 2007-02, Vol.17 (1), p.A18

2007

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Transthyretin messenger ribonucleic acid expression in the pancreas and in endocrine tumors of the pancreas and gut

The journal of clinical endocrinology and metabolism, 1990-10, Vol.71 (4), p.875-880

1990

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P-02 NRAS and BRAF mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing

Melanoma research, 2007-02, Vol.17 (1), p.A17-A18

2007

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Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma

International journal of cancer, 2000-08, Vol.87 (4), p.463-467

2000

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Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

Genes chromosomes & cancer, 2001-06, Vol.31 (2), p.107-116

2001

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Screening of N-ras Codon 61 Mutations in Paired Primary and Metastatic Cutaneous Melanomas

Clinical cancer research, 2002-11, Vol.8 (11), p.3468

2002

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Cytoplasmic and nuclear accumulation of β-catenin is rarely caused by CTNNBI exon 3 mutations in cutaneous malignant melanoma

International journal of cancer, 2001, Vol.92 (6), p.839-842

2001

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Re: Biologic and Biochemical Analyses of p16INK4a Mutations From Primary Tumors

JNCI : Journal of the National Cancer Institute, 2000-05, Vol.92 (9), p.758a-759

2000

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Human cutaneous melanoma; a review of NRAS and BRAF mutation frequencies in relation to histogenetic subclass and body site

NRAS and BRAF Mutations Arise Early during Melanoma Pathogenesis and Are Preserved throughout Tumor Progression

N-ras Mutations are Common in Melanomas from Sun-Exposed Skin of Humans but Rare in Mucosal Membranes or Unexposed Skin

Biallelic Deletions in INK4 in Cutaneous Melanoma Are Common and Associated with Decreased Survival

NRAS and BRAF mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing

Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma

Cytoplasmic and nuclear accumulation of ?-catenin is rarely caused byCTNNB1 exon 3 mutations in cutaneous malignant melanoma

Screening of N-ras codon 61 Mutations in paired primary and metastatic cutaneous melanomas: Mutations occur early and persist throughout tumor progression

Cytoplasmic and nuclear accumulation of β‐catenin is rarely caused by CTNNB1 exon 3 mutations in cutaneous malignant melanoma

Frequency of UV-Inducible NRAS Mutations in Melanomas of Patients With Germline CDKN2A Mutations

CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas

Pyrosequencing as an Alternative to Single-Strand Conformation Polymorphism Analysis for Detection of N-ras Mutations in Human Melanoma Metastases

Hereditary cutaneous melanoma

Screening of Germline Mutations in the CDKN2A and CDKN2B Genes in Swedish Families With Hereditary Cutaneous Melanoma

Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patients

Germline CDKN2A mutations are rare in child and adolescent cutaneous melanoma

p53 protein expression and TP53 mutations in malignant melanomas of sun-sheltered mucosal membranes versus chronically sun-exposed skin

P-03 CCND1 A870G polymorphism and age of onset of melanoma

Transthyretin messenger ribonucleic acid expression in the pancreas and in endocrine tumors of the pancreas and gut

P-02 NRAS and BRAF mutations in melanoma tumours in relation to clinical characteristics: a study based on mutation screening by pyrosequencing

Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma

Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

Screening of N-ras Codon 61 Mutations in Paired Primary and Metastatic Cutaneous Melanomas

Cytoplasmic and nuclear accumulation of β-catenin is rarely caused by CTNNBI exon 3 mutations in cutaneous malignant melanoma

Re: Biologic and Biochemical Analyses of p16INK4a Mutations From Primary Tumors

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