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Use of chromogenic in situ hybridization to identify MYCN gene copy number in neuroblastoma using routine tissue sections

The American journal of surgical pathology, 2006-05, Vol.30 (5), p.635-642

2006

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Establishment of a Cytokine-Producing Anaplastic Large-Cell Lymphoma Cell Line Containing the t(2;5) Translocation: Potential Role of Cytokines in Clinical Manifestations

Leukemia & lymphoma, 2001-02, Vol.40 (5-6), p.599-611

2001

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Imatinib mesylate: An attractive alternative in young children with large, surgically challenging dermatofibrosarcoma protuberans

Pediatric blood & cancer, 2005-05, Vol.44 (5), p.511-515

2005

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Mutational specificity of alkylating agents and the influence of DNA repair

Environmental and molecular mutagenesis, 1990, Vol.15 (2), p.107-122

1990

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Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas

Genes chromosomes & cancer, 2003-01, Vol.36 (1), p.7-16

2003

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Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant

The Journal of pediatrics, 1996-04, Vol.128 (4), p.579-586

1996

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Primitive neuroectodermal tumors of the cerebrum and cerebellum: absence of t(11;22) translocation by RT-PCR analysis

Modern pathology, 1995-06, Vol.8 (5), p.488

1995

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Association of the t(12;22)(q13;q12) EWS/ATF1 rearrangement with polyphenotypic round cell sarcoma of bone: a case report

The American journal of surgical pathology, 2005-12, Vol.29 (12), p.1673-1679

2005

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Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies

Journal of clinical oncology, 2009-05, Vol.27 (15_suppl), p.11107-11107

2009

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Stem cell enrichment approaches

Seminars in cancer biology, 2007-06, Vol.17 (3), p.257-264

2007

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An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma

Genes chromosomes & cancer, 2005-04, Vol.42 (4), p.392-403

2005

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Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Oncogene, 2002-05, Vol.21 (19), p.3029-3037

2002

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Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Oncogene, 2002-05, Vol.21 (19), p.3029-3037

2002

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HER2 amplification and overexpression is not present in pediatric osteosarcoma: a tissue microarray study

Pediatric and developmental pathology, 2005-09, Vol.8 (5), p.525-532

2005

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Defining a 0.5-Mb Region of Genomic Gain on Chromosome 6p22 in Bladder Cancer by Quantitative-Multiplex Polymerase Chain Reaction

The American journal of pathology, 2004, Vol.164 (1), p.285-293

2004

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Primary subcutaneous primitive neuroectodermal tumor with aggressive behavior and an unusual karyotype: case report

Pediatric and developmental pathology, 2004-09, Vol.7 (5), p.538-545

2004

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Application of Comparative Genomic Hybridization, Spectral Karyotyping, and Microarray Analysis in the Identification of Subtype-Specific Patterns of Genomic Changes in Rhabdomyosarcoma

Neoplasia (New York, N.Y.), 1999-08, Vol.1 (3), p.262-275

1999

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Morphological and phenotypic features in pediatric large cell lymphoma and their correlation with ALK expression and the t(2;5)(p23;q35) translocation

Pediatric and developmental pathology, 2001-03, Vol.4 (2), p.129-137

2001

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Increased detection of metastatic melanoma in pediatric sentinel lymph node biopsies using RT-PCR on paraffin-embedded tissue

Applied immunohistochemistry & molecular morphology, 2010-07, Vol.18 (4), p.365-370

2010

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C-kit expression and mutational analysis in medulloblastoma

Pediatric and developmental pathology, 2004-09, Vol.7 (5), p.493-498

2004

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Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome

Cancer, 2001-06, Vol.91 (11), p.2156-2164

2001

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Oncogene amplification in medulloblastoma: analysis of a case by comparative genomic hybridization and fluorescence in situ hybridization

Pathology, 1999-11, Vol.31 (4), p.337-344

1999

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Comparative genomic hybridization analysis of pediatric adamantinomatous craniopharyngiomas and a review of the literature

Journal of neurosurgery, 2004-08, Vol.101 (1 Suppl), p.85-90

2004

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Detection of novel variant TMPRSS2 /ERG fusion transcripts suggests independent genomic alterations may underlie origin of multi-centric prostate cancer

Journal of clinical oncology, 2006-06, Vol.24 (18_suppl), p.10029-10029

2006

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Molecular Detection of the (2;5) Translocation of Non-Hodgkin's Lymphoma by Reverse Transcriptase-Polymerase Chain Reaction

Blood, 1995-06, Vol.85 (12), p.3416-3422

1995

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Use of chromogenic in situ hybridization to identify MYCN gene copy number in neuroblastoma using routine tissue sections

Establishment of a Cytokine-Producing Anaplastic Large-Cell Lymphoma Cell Line Containing the t(2;5) Translocation: Potential Role of Cytokines in Clinical Manifestations

Imatinib mesylate: An attractive alternative in young children with large, surgically challenging dermatofibrosarcoma protuberans

Mutational specificity of alkylating agents and the influence of DNA repair

Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas

Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant

Primitive neuroectodermal tumors of the cerebrum and cerebellum: absence of t(11;22) translocation by RT-PCR analysis

Association of the t(12;22)(q13;q12) EWS/ATF1 rearrangement with polyphenotypic round cell sarcoma of bone: a case report

Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies

Stem cell enrichment approaches

An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma

Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

HER2 amplification and overexpression is not present in pediatric osteosarcoma: a tissue microarray study

Defining a 0.5-Mb Region of Genomic Gain on Chromosome 6p22 in Bladder Cancer by Quantitative-Multiplex Polymerase Chain Reaction

Primary subcutaneous primitive neuroectodermal tumor with aggressive behavior and an unusual karyotype: case report

Application of Comparative Genomic Hybridization, Spectral Karyotyping, and Microarray Analysis in the Identification of Subtype-Specific Patterns of Genomic Changes in Rhabdomyosarcoma

Morphological and phenotypic features in pediatric large cell lymphoma and their correlation with ALK expression and the t(2;5)(p23;q35) translocation

Increased detection of metastatic melanoma in pediatric sentinel lymph node biopsies using RT-PCR on paraffin-embedded tissue

C-kit expression and mutational analysis in medulloblastoma

Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome

Oncogene amplification in medulloblastoma: analysis of a case by comparative genomic hybridization and fluorescence in situ hybridization

Comparative genomic hybridization analysis of pediatric adamantinomatous craniopharyngiomas and a review of the literature

Detection of novel variant TMPRSS2 /ERG fusion transcripts suggests independent genomic alterations may underlie origin of multi-centric prostate cancer

Molecular Detection of the (2;5) Translocation of Non-Hodgkin's Lymphoma by Reverse Transcriptase-Polymerase Chain Reaction

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