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pro vyhledávání: '"Genetics of cancer"'
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Autor:
zur Nieden, Andrea1 andrea.zur.nieden@soziologie.uni-freiburg
Publikováno v:
BioSocieties. Dec2016, Vol. 11 Issue 4, p535-539. 5p.
Autor:
Matthew L. Hedberg, Corbett T. Berry, Ata S. Moshiri, Yan Xiang, Christopher J. Yeh, Cem Attilasoy, Brian C. Capell, John T. Seykora
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3478 (2022)
Non-melanoma skin cancers are cutaneous malignancies representing the most common form of cancer in the United States. They are comprised predominantly of basal cell carcinomas and squamous cell carcinomas (cSCC). The incidence of cSCC is increasing,
Externí odkaz:
https://doaj.org/article/d49a89e0847c408c8dc15f3e734081a8
Autor:
Melissa Solarte, Carolina Cortes-Urrea, Nelson Rivera Franco, Guillermo Barreto, Pedro A. Moreno
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 4 (2020)
Abstract Breast cancer is the leading cause of death by cancer among women in less developed regions. In Colombia, few published studies have applied next-generation sequencing technologies to evaluate the genetic factors related to breast cancer. Th
Externí odkaz:
https://doaj.org/article/5d5d23d20e5341ed9d11dd919a7c1e3f
Autor:
Giulia Ceglie, Giada Del Baldo, Emanuele Agolini, Martina Rinelli, Antonella Cacchione, Francesca Del Bufalo, Maria Vinci, Roberto Carta, Luigi Boccuto, Evelina Miele, Angela Mastronuzzi, Franco Locatelli, Andrea Carai
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Pediatric High-Grade Gliomas (pHGG) are among the deadliest childhood brain tumors and can be associated with an underlying cancer predisposing syndrome. The thorough understanding of these syndromes can aid the clinician in their prompt recognition,
Externí odkaz:
https://doaj.org/article/d07abd43c62743318c21bb4489f59dbe
Autor:
Patrick M Lynch, JD, MD
Publikováno v:
Revista Médica Clínica Las Condes, Vol 28, Iss 4, Pp 500-511 (2017)
Hereditary Nonpolyposis Colorectal Cancer (HNPCC or “Lynch syndrome”), involving pathogenic variants in the Mismatch Repair (MMR) genes, is the most common inherited condition that predisposed to colorectal adenomas and colorectal cancer. In this
Externí odkaz:
https://doaj.org/article/b13240dcb0424078a14946eabf647d5f
Применение внутрибрюшинно дигидробромида 2-(3,4-дигидроксифенил)-9-диэтиламиноэтилимидазо[1,2-a]бензимидазола в качестве антипролифератив
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fabe041028e2da95985709b1efe0c35f
Autor:
BURNS, ANGUS CHARLES
Modern electric lighting environments can disrupt the human circadian system by blurring the distinction between day and night. Many psychiatric disorders are characterised by disrupted circadian rhythms. In this thesis, we examined the association o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ebb3729e6827cc21bfb0f53b905d06f
Autor:
TILLER, JANE MAREE
Genetic testing has the potential to save lives through prevention or early treatment of disease. However, numerous ethical, legal and social issues affect the implementation and effectiveness of genomic medicine. The primary issues covered in this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c336cf34ff4c3245ce2a88e11e1d2af
Autor:
MCKAIGE, EMILY ANNE
Inherited skeletal myopathies are muscle diseases characterised by muscle wasting and movement difficulties. Currently, many myopathy patients do not have a genetic diagnosis and for those that do have a diagnosis, we do not understand why these gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25cd7d684accc55a926dd280ddfeeabd