Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Aurelia M Meloni"'
Autor:
Aurelia M Meloni-Ehrig
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b68578d170bada791084f313ea00547e
https://doi.org/10.4267/2042/66950
https://doi.org/10.4267/2042/66950
Autor:
Aurelia M. Meloni-Ehrig, Carlos A. Tirado, Kuoping Chen, Jennifer Jahn, Stephany Suchan, Jay Scheerle, Maria Gabriela Crosby, Holly Meany, Nita Seibel, David Leitenberg, Deborah W. Heritage, Philip N. Mowrey
Publikováno v:
Cancer Genetics and Cytogenetics. 161:82-85
We present a case of del(14)(q21) as a sole abnormality in a 4-year-old boy diagnosed with precursor B-cell acute lymphoblastic leukemia (pre-B ALL). To our knowledge, this is the first case of isolated del(14)(q21) in pre-B ALL. Two pretreatment bon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37013e1f2ada16c6373476f1a09592d
https://doi.org/10.1016/j.cancergencyto.2004.12.022
https://doi.org/10.1016/j.cancergencyto.2004.12.022
Autor:
Carlos A. Tirado, Jennifer A. Jahn, Jay Scheerle, Maya Eid, Robert J. Meister, Robert J. Christie, Calvin D. Croft, Steven Wallingford, Deborah W. Heritage, Philip N. Mowrey, Aurelia M. Meloni-Ehrig
Publikováno v:
Cancer Genetics and Cytogenetics. 161:70-73
Fluorescence in situ hybridization (FISH) analysis of the bone marrow of a 24-year-old man diagnosed with acute promyelocytic leukemia (APL) revealed a variant pattern with one fusion signal instead of the typical two fusions expected with the probe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a86093baf54e4c6b9ee9aabd788f2b29
https://doi.org/10.1016/j.cancergencyto.2005.01.005
https://doi.org/10.1016/j.cancergencyto.2005.01.005
Autor:
James C. Lynch, Joanne Degenhardt, Mari Nelson, Sarah J. Swarts, Gerhard Maale, Cary J. Buresh, Suzanne S. Spanier, James R. Neff, Julia A. Bridge, Aurelia M Meloni
Publikováno v:
The American Journal of Pathology. 154:729-733
Trisomy 8 and trisomy 20 are nonrandom aberrations in desmoid tumors. The presence of these trisomies in related benign fibrous lesions of bone has not been previously addressed. In this study, 22 specimens from 19 patients diagnosed with desmoid tum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc450c0acf3e4d608e6f75b5f0b8e4dc
https://doi.org/10.1016/s0002-9440(10)65319-9
https://doi.org/10.1016/s0002-9440(10)65319-9
Autor:
Michael D. Hughson, Steven A. Bigler, Avery A. Sandberg, Kathleen G. Dickman, Aurelia M. Meloni
Publikováno v:
Cancer Genetics and Cytogenetics. 106:93-104
Clear-cell and papillary renal cell carcinomas (RCCs) have specific genetic changes that allow them to be classified on the basis of histopathology and on the basis of cytogenetic and molecular genetic findings. Clear-cell carcinomas are characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e17bbb207a5e6cc52bdb785573b171c9
https://doi.org/10.1016/s0165-4608(98)00068-5
https://doi.org/10.1016/s0165-4608(98)00068-5
Autor:
Aurelia M. Meloni, Yavuz Ozisik, Avery A. Sandberg, Kristine L. Kingsley, Charles H. Bush, Suzanne S. Spanier
Publikováno v:
Cancer Genetics and Cytogenetics. 105:128-133
Ollier disease is an uncommon, nonhereditary developmental disorder affecting enchondral ossification. Cytogenetic analysis of low-grade chondrosarcoma in a patient with Ollier disease (multiple enchondromatosis) revealed an interstitial deletion, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef79d940cb0dfcd80422216529597b15
https://doi.org/10.1016/s0165-4608(98)00027-2
https://doi.org/10.1016/s0165-4608(98)00027-2
Autor:
John F. Stone, Joseph S Bennett, Jesse D. Cohen, Aurelia M. Meloni-Ehrig, Avery A. Sandberg, Mathilda Notohamiprodjo, Rodman Morgan, Robert T Schuster, Zhong Chen
Publikováno v:
Cancer Genetics and Cytogenetics. 101:148-151
Three cases of acute nonlymphocytic leukemia with a Philadelphia chromosome (Ph) as a secondary abnormality are reported. The Ph was late-appearing in one patient and appeared as an additional anomaly in the other two patients. Fluorescence in situ h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d121c266197cb98ccf8c31ea4936d5
https://doi.org/10.1016/s0165-4608(97)00262-8
https://doi.org/10.1016/s0165-4608(97)00262-8
Autor:
Marcus A. Erling, Ronald S. Oseas, Stephen G. Jolley, Troy M Reyna, Aurelia M. Meloni, Ronald M. Kline, Avery A. Sandberg
Publikováno v:
Cancer Genetics and Cytogenetics. 98:97-101
Cytogenetic analysis performed on a 14-month-old boy with a primary retroperitoneal/paraspinal alveolar rhabdomyosarcoma showed the presence of a der(13)t(1;13)(q23;q32) resulting in partial trisomy of the 1q23→qter region and loss of the 13q32→q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54278126ffde9a6d1fc5d040156b1fbd
https://doi.org/10.1016/s0165-4608(96)00414-1
https://doi.org/10.1016/s0165-4608(96)00414-1
Publikováno v:
Cancer Genetics and Cytogenetics. 87:133-139
Nonpapillary renal cell carcinomas (RCCs) are characterized by deletions of the short arm of chromosome 3 (3p) and papillary RCCs by increased numbers of selected chromosomes. Although recent molecular genetic studies have reported some papillary RCC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a287772abc15961ac9212b3f868877c
https://doi.org/10.1016/0165-4608(95)00274-x
https://doi.org/10.1016/0165-4608(95)00274-x
Autor:
Gregory Y. Lauwers, Aurelia M. Meloni, Avery A. Sandberg, Jaime L. Betz, Stephen Vogel, John F. Stone, Larry D. Grant
Publikováno v:
The American Journal of Surgical Pathology. 20:339-345
We report on a solid and cystic papillary epithelial neoplasm of the pancreas containing the unbalanced chromosome translocation der(17)t(13;17)(q14;p11), resulting in loss of 13q14-->qter and 17p11-->pter. Although the clinical and pathologic charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c9bff6252cafd61bcc6d2723c31971
https://doi.org/10.1097/00000478-199603000-00011
https://doi.org/10.1097/00000478-199603000-00011