Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Stephen R. Moore"'
Autor:
Joshua L. Deignan, Vimla Aggarwal, Allen E. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao, Kristy R. Crooks, Kristen L. Deak, Daniela Del Gaudio, Birgit Funke, Nicole L. Hoppman, Vanessa Horner, Robert B. Hufnagel, Colleen Jackson-Cook, Prasad Koduru, Marco L. Leung, Shibo Li, Pengfei Liu, Minjie Luo, Rong Mao, Heather Mason-Suares, Fady M. Mikhail, Stephen R. Moore, Rizwan C. Naeem, Laura M. Pollard, Elena A. Repnikova, Lina Shao, Brandon M. Shaw, Shashirekha Shetty, Teresa A. Smolarek, Elizabeth Spiteri, Jessica Van Ziffle, Gail H. Vance, Cindy L. Vnencak-Jones, Eli S. Williams
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101820- (2024)
Purpose: The specialty of Laboratory Genetics and Genomics (LGG) was created in 2017 in an effort to reflect the increasing convergence in technologies and approaches between clinical molecular genetics and clinical cytogenetics. However, there has n
Externí odkaz:
https://doaj.org/article/06de2e3b5f9244b89cae6954ab35c034
Publikováno v:
Diagnostic Pathology, Vol 14, Iss 1, Pp 1-16 (2019)
Abstract Insights into the molecular underpinnings of primary central nervous system tumors have radically changed the approach to tumor diagnosis and classification. Diagnostic emphasis has shifted from the morphology of a tumor under the microscope
Externí odkaz:
https://doaj.org/article/7a64f7ed2ca14eb0a36d5c3f2a106778
Autor:
Tadayuki Akagi, Lee-Yung Shih, Seishi Ogawa, Joachim Gerss, Stephen R. Moore, Rhona Schreck, Norihiko Kawamata, Der-Cherng Liang, Masashi Sanada, Yasuhito Nannya, Stefan Deneberg, Vasilios Zachariadis, Ann Nordgren, Jee Hoon Song, Martin Dugas, Sören Lehmann, H. Phillip Koeffler
Publikováno v:
Haematologica, Vol 94, Iss 9 (2009)
Translocation of chromosomes 8 and 21, t(8;21), resulting in the AML1-ETO fusion gene, is associated with acute myeloid leukemia. We searched for additional genomic abnormalities in this acute myeloid leukemia subtype by performing single nucleotide
Externí odkaz:
https://doaj.org/article/69368bc8eb154402be51df8a86302fa6
Autor:
Wei Xie, Philipp W. Raess, Jennifer Dunlap, Cristina Magallanes Hoyos, Hongmei Li, Peng Li, Ronan Swords, Susan B. Olson, Fei Yang, Tauangtham Anekpuritanang, Shimin Hu, Joanna Wiszniewska, Guang Fan, Richard D. Press, Stephen R. Moore
Publikováno v:
Leukemia & Lymphoma. 63:1907-1916
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8747a11ec5869c87a5071674ccf47708
https://doi.org/10.1080/10428194.2022.2047672
https://doi.org/10.1080/10428194.2022.2047672
Autor:
Stephen R. Moore
Publikováno v:
Renewable Agriculture and Food Systems. 25:181-188
Modern agriculture relies heavily on fossil energy for food production. Reducing fossil energy and replacing that energy with renewable energy is critical in attaining a sustainable food system. Hand-scale intensive food production offers a reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8bba1ecaf2c4d36918e3056375e0099
https://doi.org/10.1017/s1742170510000098
https://doi.org/10.1017/s1742170510000098
Autor:
John M. Graham, Stephen R. Moore, David L. Rimoin, Joseph N. Peeden, Ralph S. Lachman, Areeg El-Gharbawy
Publikováno v:
American Journal of Medical Genetics Part A. :169-174
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal dysplasia due to mutations causing haploinsufficiency of RUNX2, an osteoblast transcription factor specific for bone and cartilage. The classic form of CCD is characterized by delaye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::947638c9f90870181947adc76500f231
https://doi.org/10.1002/ajmg.a.33146
https://doi.org/10.1002/ajmg.a.33146
Autor:
Joachim Gerss, Lee Yung Shih, Tadayuki Akagi, Vasilios Zachariadis, Yasuhito Nannya, Rhona Schreck, Stephen R. Moore, Seishi Ogawa, H. Phillip Koeffler, Stefan Deneberg, Martin Dugas, Ann Nordgren, Soren Lehmann, Jee Hoon Song, Norihiko Kawamata, Der Cherng Liang, Masashi Sanada
Publikováno v:
Haematologica. 94(9):1301-1309
金沢大学医薬保健研究域医学系
Translocation of chromosomes 8 and 21, t(8;21), resulting in the AML1-ETO fusion gene, is associated with acute myeloid leukemia. We searched for additional genomic abnormalities in this acute myeloid l
Translocation of chromosomes 8 and 21, t(8;21), resulting in the AML1-ETO fusion gene, is associated with acute myeloid leukemia. We searched for additional genomic abnormalities in this acute myeloid l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ee3df80775e4ea1f479ab4cd52ac738
http://hdl.handle.net/2297/19612
http://hdl.handle.net/2297/19612
Autor:
Dolores Bobadilla, Ralph J. Tuthill, David D. Smith, Stephen R. Moore, Vernon K. Sondak, Marilyn L. Slovak, Jeffrey A. Sosman, Diane L. Persons, Jim Moon, Victoria Bedell, Sandra R. Wolman
Publikováno v:
Clinical Cancer Research. 14:2927-2935
Purpose: Gene copy number alteration (CNA) is common in malignant melanoma and is associated with tumor development and progression. The concordance between molecular cytogenetic techniques used to determine CNA has not been evaluated on a large set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfca0b84791a95b3496547787ed43fc5
https://doi.org/10.1158/1078-0432.ccr-07-4068
https://doi.org/10.1158/1078-0432.ccr-07-4068
Autor:
Thomas H, Long, Helen, Lawce, Connie, Durum, Stephen R, Moore, Susan B, Olson, Ken, Gatter, Megan L, Troxell
Publikováno v:
American journal of clinical pathology. 144(2)
Human epidermal growth factor receptor 2 (HER2, ERBB2) testing is an important prognostic/predictive marker in breast cancer management, especially in selecting HER2-targeted treatment. American Society of Clinical Oncology (ASCO)/College of American
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e846bd1fd034a4c85fd461170ca3ac9a
https://pubmed.ncbi.nlm.nih.gov/26185310
https://pubmed.ncbi.nlm.nih.gov/26185310
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 600:113-124
Genomic instability is observed in tumors and in a large fraction of the progeny surviving irradiation. One of the best-characterized phenotypic manifestations of genomic instability is delayed chromosome aberrations. Our working hypothesis for the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c5035aeb9c3fb498836355886f2f966
https://doi.org/10.1016/j.mrfmmm.2006.03.006
https://doi.org/10.1016/j.mrfmmm.2006.03.006