نتایج جستجو برای: deletion 6q

تعداد نتایج: 79891  

Journal: :American journal of medical genetics 1999
M Martinez L R Goldin Q Cao J Zhang A R Sanders D J Nancarrow J M Taylor D F Levinson A Kirby R R Crowe N C Andreasen D W Black J M Silverman D P Lennon D A Nertney D M Brown B J Mowry E S Gershon P V Gejman

Evidence for suggestive linkage to schizophrenia with chromosome 6q markers was previously reported from a two-stage approach. Using nonparametric affected sib pairs (ASP) methods, nominal p-values of 0.00018 and 0.00095 were obtained in the screening (81 ASPs; 63 independent) and the replication (109 ASPs; 87 independent) data sets, respectively. Here, we report a follow-up study of this 50cM ...

2005
Paul B. Sinclair Christine J. Harrison Marie Jarosová Letizia Foroni

Recurrent chromosomal translocations are important diagnostic and prognostic markers contributing to the management of patients with a variety of hematologic malignancies. Moreover, the molecular characterization of breakpoints from such rearrangements has led to the identification of oncogenes and to the design of novel therapeutic approaches and sensitive polymerase chain reaction (PCR)based ...

Journal: :Cancer Genetics and Cytogenetics 1983

2017
Anikó Kovács Fredrik Persson Marta Persson Mattias K. Andersson Göran Stenman

The incidence of synchronous bilateral breast carcinomas (BBCs) has increased with a more frequent use of magnetic resonance imaging screening of the contralateral breast in women with newly diagnosed breast cancer. A total of 30% of all BBCs occur synchronously. In the present study, we describe a unique case of synchronous BBC in a 59-year-old previously healthy woman with no known family his...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2001
M G Tibiletti B Bernasconi D Furlan P Bressan R Cerutti C Facco M Franchi C Riva R Cinquetti C Capella R Taramelli

PURPOSE We used conventional cytogenetics, molecular cytogenetics, and molecular genetic analyses to study the pattern of allelic loss on chromosome 6q in a cohort of borderline epithelial ovarian tumors. EXPERIMENTAL DESIGN Fifteen tumor samples were collected from patients undergoing surgery for ovarian tumors. The tumors of borderline malignancy, classified according to the standard criter...

Journal: :American journal of hematology 2013
Laura Mosca Pellegrino Musto Katia Todoerti Marzia Barbieri Luca Agnelli Sonia Fabris Giacomo Tuana Marta Lionetti Eleonora Bonaparte Silvia Maria Sirchia Vitina Grieco Gabriella Bianchino Fiorella D'Auria Teodora Statuto Carmela Mazzoccoli Luciana De Luca Maria Teresa Petrucci Fortunato Morabito Massimo Offidani Francesco Di Raimondo Antonietta Falcone Tommaso Caravita Paola Omedè Mario Boccadoro Antonio Palumbo Antonino Neri

Primary plasma cell leukemia (pPCL) is a rare, yet aggressive form of de novo plasma cell tumor, distinct from secondary PCL (sPCL) which represents a leukemic transformation of pre-existing multiple myeloma (MM). Herein, we performed a comprehensive molecular analysis of a prospective series of pPCLs by means of FISH, single nucleotide polymorphism (SNP) array and gene expression profiling (GE...

Journal: :Cancer research 1997
V Boige P Laurent-Puig P Fouchet J F Fléjou G Monges P Bedossa P Bioulac-Sage F Capron A Schmitz S Olschwang G Thomas

Although the occurrence of loss of genetic material in hepatocellular carcinoma (HCC) has been documented both by cytogenetic analysis and by monitoring of allelic losses, a global overview of the extent and frequency of deletion occurring throughout the genome is not yet available. To contribute to this information, DNAs extracted from flow-sorted aneuploid nuclei from HCC and matched normal D...

Journal: :Blood 2010
Marta Salido Cristina Baró David Oscier Kostas Stamatopoulos Judith Dierlamm Estela Matutes Alexandra Traverse-Glehen Francoise Berger Pascale Felman Catherine Thieblemont Stefan Gesk Anastasia Athanasiadou Zadie Davis Anne Gardiner Fuensanta Milla Ana Ferrer Manuela Mollejo Maria José Calasanz Lourdes Florensa Blanca Espinet Elisa Luño Iwona Wlodarska Gregor Verhoef Marta García-Granero Antonio Salar Theodora Papadaki Sergio Serrano Miguel A Piris Francesc Solé

We conducted a retrospective collaborative study to cytogenetically characterize splenic marginal zone lymphoma (SMZL) and ascertain the prognostic value of chromosomal aberrations. Of 330 cases, 72% displayed an aberrant karyotype, 53% were complex, and 29% had a single aberration. The predominant aberrations were gains of 3/3q and 12q, deletions of 7q and 6q and translocations involving 8q/1q...

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