Zobrazeno 1 - 10
of 63
pro vyhledávání: '"FH Thompson"'
Publikováno v:
Gene Amplification in Mammalian Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c9b055195d0a4f2c939a5058a573756
https://doi.org/10.1201/9781003066989-6
https://doi.org/10.1201/9781003066989-6
Autor:
FH Thompson, Stanley P. L. Leong, Mikel Aickin, Jerry L. Bangert, Mark A. Nelson, Michael D. Radmacher, Raymond Taetle, Lawrence Adair, Jeffrey M. Trent, Sydney E. Salmon, Lita Panda, Jin Ming Yang, Denise J. Roe, Richard Simon, Julia Emerson
Publikováno v:
Cancer Genetics and Cytogenetics. 122:101-109
We report the cytogenetic abnormalities from a series of 206 primary malignant melanoma specimens referred to a single institution. A total of 169 out of 206 unique cases had chromosome breakpoints. A previously described statistical method was used
Autor:
Denise J. Roe, Raymond Taetle, FH Thompson, John R. Davis, Jeffrey M. Trent, David S. Alberts, Lita Panda, Julia Emerson, Mikel Aickin
Publikováno v:
Genes, Chromosomes and Cancer. 25:46-52
In a large series of ovarian carcinomas from 244 patients, 134 cases had chromosome rearrangements. We showed before that the pattern of chromosome breakpoints involved 21 separate chromosome regions nonrandomly and, in 90% of cases with breaks, the
Autor:
Raymond Taetle, Marianne Broome-Powell, Jin Ming Yang, FH Thompson, Maria E. Ariza, Mark A. Nelson, Julie Wymer, Jeffrey M. Trent, Vincent J. Kidd, Kathy Massey-Brown, Jill M. Lahti, John Easton
Publikováno v:
Cancer Genetics and Cytogenetics. 108:91-99
The two genes encoding the PITSLRE protein kinase isoforms, CDC2L1 and CDC2L2, are localized to human chromosome band 1p36. The PITSLRE protein kinases are a part of the p34cdc2 supergene family. Several protein products of the CDC2L locus may be eff
Publikováno v:
Clinical Genetics. 50:545-547
Conotruncal anomaly face syndrome (CTAFS) was distinguished from velo-cardio-facial syndrome (VCFS) in a bind study, yet shared the finding of 22q11.2 deletions. This work has been extended to show that the 22q11.2 deletions in CTAFS greatly overlap
Publikováno v:
Insect Biochemistry and Molecular Biology. 28:733-738
The biosynthesis of lipophorin of the yellow fever mosquito, Aedes aegypti, was investigated. Fat bodies were incubated in vitro with radiolabeled methionine and cysteine, and radiolabeled proteins secreted into the medium were analyzed by density gr
Autor:
Jeffrey M. Trent, Mark A. Nelson, David S. Alberts, Raymond Taetle, Katherine M. Scott, Yun Liu, Julia Emerson, FH Thompson, Kathy Massey-Brown, Ronald S. Weinstein
Publikováno v:
Cancer Genetics and Cytogenetics. 96:106-110
In a series of 128 karyotyped ovarian carcinomas, 42% of cases with chromosome 1 clonal structural abnormalities had breaks at band 1p36 (usually involving translocations of unknown material). Fluorescent in situ hybridization (FISH) studies using co
Autor:
Robert T. Dorr, Evan M. Hersh, Cynthia S. Johnson, Rebecca A. Curtis, Charles W. Taylor, Carole Y. Funk, Gillian Paine-Murrieta, FH Thompson, Marialouisa H. A. Lopez
Publikováno v:
Cancer Chemotherapy and Pharmacology. 40:209-214
Purpose: To test a number of established human tumor cell lines and early passage breast cancer (UACC2150) and melanoma cells (UACC1273) for growth in the scid mouse and the tumors' response to conventional chemotherapeutic drugs. Methods: Establishe
Autor:
Julia Emerson, FH Thompson, Jeffrey M. Trent, Mikel Aickin, Raymond Taetle, Laurence Adair, Stanley P.L. Leong, Mark A. Nelson
Publikováno v:
Surgical Clinics of North America. 76:1257-1271
Unlike leukemia, in which specific reciprocal translocations are frequently observed, melanomas involve complex recurring chromosome anomalies. Analysis of the constituted genome of melanoma patients should identify cancer susceptibility genes and at
Autor:
Julie Wymer, Ronald S. Weinstein, Celia A. Balfour, David S. Alberts, Jin Ming Yang, Laurence Adair, Raymond Taetle, Jeffrey M. Trent, Mark A. Nelson, Yun Liu, Julia Emerson, FH Thompson, Xin Yuan Guan, Kathy Massey
Publikováno v:
Cancer Genetics and Cytogenetics. 87:55-62
In this study of ovarian carcinoma, we extended previous findings by performing FISH using chromosome 19 paint and microFISH probes and patient samples with and without abnormalities of chromosome 19 identified by G-banding. Karyotype interpretations