Topic: Male

Journal: Cancer Genetics and Cytogenetics

Documents

A list of abstracts that contain a topic of "Male" and a journal name of "Cancer Genetics and Cytogenetics".

• Lymphoplasmacytic Lymphoma/Waldenström Macroglobulinemia with Inv(16)(P13q22) As a Sole Genetic Abnormality.

  PMID: 17452259

• A (9;11)(Q34;q13) Translocation in a Hibernoma.

  PMID: 17011989

• A Diminutive Chromosome 21 Centromere in Acute Lymphoblastic Leukemia.

  PMID: 16682292

• Myelodysplastic Syndrome Associated with Monosomy 7 in Childhood: a Retrospective Study.

  PMID: 17074595

• Lack of Association Between Dna Repair Gene Ercc1 Polymorphism and Risk of Lung Cancer in a Chinese Population.

  PMID: 16364765

• Cytogenetics of Agnogenic Myeloid Metaplasia: a Study of 61 Patients.

  PMID: 17284371

• A Case of Chronic Myeloproliferative Syndrome Followed by Precursor T-cell Acute Lymphoblastic Leukemia.

  PMID: 17498558

• Numerical Aberrations of Chromosome 8 Detected by Conventional Cytogenetics and Fluorescence in Situ Hybridization in Individuals from Northern Brazil with Gastric Adenocarcinoma.

  PMID: 16875936

• Chromosome Analysis and Molecular Cytogenetic Investigations of an Epithelioid Hemangioendothelioma.

  PMID: 16938576

• Hmga2 Expression in a Canine Model of Prostate Cancer.

  PMID: 17854662

• Transformed Follicular Lymphoma with Concurrent T(2;3), T(8;14) and T(14;18).

  PMID: 17284373

• Additional Cytogenetic Changes and Previous Genotoxic Exposure Predict Unfavorable Prognosis in Myelodysplastic Syndromes and Acute Myeloid Leukemia with Der(1;7)(Q10;p10).

  PMID: 16527611

• Translocation (3;8)(Q26;q24): a Recurrent Chromosomal Abnormality in Myelodysplastic Syndrome and Acute Myeloid Leukemia.

  PMID: 16616115

• Overexpression of Bubr1 is Associated with Chromosomal Instability in Bladder Cancer.

  PMID: 17350465

• Bone Morphogenetic Protein Antagonist Gene Nog is Involved in Myeloproliferative Disease Associated with Myelofibrosis.

  PMID: 17889703

• Two Neurofibromatosis Type 1 Cases Associated with Rhabdomyosarcoma of Bladder, One with a Large Deletion in the Nf1 Gene.

  PMID: 16434322

• 6q Deletion Discriminates Waldenström Macroglobulinemia from Igm Monoclonal Gammopathy of Undetermined Significance.

  PMID: 16938573

• Two Novel Translocations Disrupt the Runx1 Gene in Acute Myeloid Leukemia.

  PMID: 17854666

• Apc and Ctnnb1 Mutations Are Rare in Sporadic Ependymomas.

  PMID: 16843107

• Effects of Cyclin D1 (Ccnd1) Polymorphism on Susceptibility to Lung Cancer in a North Indian Population.

  PMID: 17011980

• Serial Cytogenetic Alterations Resulting in Transformation of a Low-grade Follicular Lymphoma to Burkitt Lymphoma.

  PMID: 17011985

• Multitarget Fluorescence in Situ Hybridization and Melanoma Antigen Genes Analysis in Primary Bladder Carcinoma.

  PMID: 16364760

• Interphase Fish Analysis of Pten in Histologic Sections Shows Genomic Deletions in 68% of Primary Prostate Cancer and 23% of High-grade Prostatic Intra-epithelial Neoplasias.

  PMID: 16938570

• Characterizing Genetically Stable and Unstable Gastric Cancers by Microsatellites and Array Comparative Genomic Hybridization.

  PMID: 17011984

• Cytogenetic Anomalies in Hyaline Vascular Castleman Disease: Report of Two Cases with Reappraisal of Histogenesis.

  PMID: 16434312

• Complex Secondary Chromosome Abnormalities in Advanced Stage Anaplastic Large Cell Lymphoma of Children and Adolescents: a Report from Ccg-e08.

  PMID: 17116485

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