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Distinct Sets of Genetic Alterations in Melanoma

The New England journal of medicine, 2005-11, Vol.353 (20), p.2135-2147

2005

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Genomic Profiling of Isolated Circulating Tumor Cells from Metastatic Breast Cancer Patients

Cancer research (Chicago, Ill.), 2013-01, Vol.73 (1), p.30-40

2013

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Isolation and genomic analysis of circulating tumor cells from castration resistant metastatic prostate cancer

BMC cancer, 2012-02, Vol.12 (1), p.78-78, Article 78

2012

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High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization

American journal of human genetics, 2005-02, Vol.76 (2), p.312-326

2005

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The Stromal Proteinase MMP3/Stromelysin-1 Promotes Mammary Carcinogenesis

Cell, 1999-07, Vol.98 (2), p.137-146

1999

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Molecular Cytogenetic Analysis of Spitz Nevi Shows Clear Differences to Melanoma

Journal of investigative dermatology, 1999-12, Vol.113 (6), p.1065-1069

1999

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Dual Inactivation of RB and p53 Pathways in RAS-Induced Melanomas

Molecular and Cellular Biology, 2001-03, Vol.21 (6), p.2144-2153

2001

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Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors

Science (American Association for the Advancement of Science), 1992-10, Vol.258 (5083), p.818-821

1992

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Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

Genes chromosomes & cancer, 1994-08, Vol.10 (4), p.231-243

1994

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pRb inactivation in mammary cells reveals common mechanisms for tumor initiation and progression in divergent epithelia

PLoS biology, 2004-02, Vol.2 (2), p.E22-E22

2004

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Positional Cloning of ZNF217 and NABC1: Genes Amplified at 20q13.2 and Overexpressed in Breast Carcinoma

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (15), p.8703-8708

1998

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Congenital Melanocytic Nevi Frequently Harbor NRAS Mutations but no BRAF Mutations

Journal of investigative dermatology, 2007-01, Vol.127 (1), p.179-182

2007

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Determinants of BRAF mutations in primary melanomas

JNCI : Journal of the National Cancer Institute, 2003-12, Vol.95 (24), p.1878-1880

2003

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Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy

American journal of human genetics, 2007-11, Vol.81 (5), p.1057-1069

2007

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Hidden Markov models approach to the analysis of array CGH data

Journal of multivariate analysis, 2004-07, Vol.90 (1), p.132-153

2004

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Cyclin d1 is a candidate oncogene in cutaneous melanoma

Cancer research (Chicago, Ill.), 2002-06, Vol.62 (11), p.3200-3206

2002

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Genetic Changes in Neoplasms Arising in Congenital Melanocytic Nevi : Differences Between Nodular Proliferations and Melanomas

The American journal of pathology, 2002-10, Vol.161 (4), p.1163-1169

2002

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Chromosomal gains and losses in primary cutaneous melanomas detected by comparative genomic hybridization

Cancer research (Chicago, Ill.), 1998-05, Vol.58 (10), p.2170-2175

1998

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Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation

The EMBO journal, 1998-08, Vol.17 (16), p.4657-4667

1998

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Gene amplifications characterize acral melanoma and permit the detection of occult tumor cells in the surrounding skin

Cancer research (Chicago, Ill.), 2000-04, Vol.60 (7), p.1968-1973

2000

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Quantum dots-based reverse phase protein microarray

Talanta (Oxford), 2005-09, Vol.67 (3), p.472-478

2005

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E2A Deficiency Leads to Abnormalities in αβ T-Cell Development and to Rapid Development of T-Cell Lymphomas

Molecular and cellular biology, 1997-08, Vol.17 (8), p.4782-4791

1997

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Abstract 3426: A novel approach to copy number assessment by whole genome sequencing reveals extensive spatial heterogeneity in diffuse low-grade glioma

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.3426-3426

2014

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Detection and Mapping of Amplified DNA Sequences in Breast Cancer by Comparative Genomic Hybridization

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (6), p.2156-2160

1994

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Analytical biotechnology

Current opinion in biotechnology, 2003-02, Vol.14 (1), p.3-4

2003

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Distinct Sets of Genetic Alterations in Melanoma

Genomic Profiling of Isolated Circulating Tumor Cells from Metastatic Breast Cancer Patients

Isolation and genomic analysis of circulating tumor cells from castration resistant metastatic prostate cancer

High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization

The Stromal Proteinase MMP3/Stromelysin-1 Promotes Mammary Carcinogenesis

Molecular Cytogenetic Analysis of Spitz Nevi Shows Clear Differences to Melanoma

Dual Inactivation of RB and p53 Pathways in RAS-Induced Melanomas

Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

pRb inactivation in mammary cells reveals common mechanisms for tumor initiation and progression in divergent epithelia

Positional Cloning of ZNF217 and NABC1: Genes Amplified at 20q13.2 and Overexpressed in Breast Carcinoma

Congenital Melanocytic Nevi Frequently Harbor NRAS Mutations but no BRAF Mutations

Determinants of BRAF mutations in primary melanomas

Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy

Hidden Markov models approach to the analysis of array CGH data

Cyclin d1 is a candidate oncogene in cutaneous melanoma

Genetic Changes in Neoplasms Arising in Congenital Melanocytic Nevi : Differences Between Nodular Proliferations and Melanomas

Chromosomal gains and losses in primary cutaneous melanomas detected by comparative genomic hybridization

Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation

Gene amplifications characterize acral melanoma and permit the detection of occult tumor cells in the surrounding skin

Quantum dots-based reverse phase protein microarray

E2A Deficiency Leads to Abnormalities in αβ T-Cell Development and to Rapid Development of T-Cell Lymphomas

Abstract 3426: A novel approach to copy number assessment by whole genome sequencing reveals extensive spatial heterogeneity in diffuse low-grade glioma

Detection and Mapping of Amplified DNA Sequences in Breast Cancer by Comparative Genomic Hybridization

Analytical biotechnology

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