Zobrazeno 1 - 10
of 354
pro vyhledávání: ''
Autor:
Annicotte, Jean-Sébastien1,2, Chavey, Carine1, Servant, Nadège1,2, Teyssier, Jacques1,2, Bardin, Aurélie1, Licznar, Anne1, Badia, Eric1, Pujol, Pascal1,3, Vignon, Françoise1, Maudelonde, Thierry1,3, Lazennec, Gwendal1, Cavailles, Vincent1, Fajas, Lluis1,2,3 fajas@montp.inserm.fr
Publikováno v:
Oncogene. 12/8/2005, Vol. 24 Issue 55, p8167-8175. 9p. 7 Diagrams.
Autor:
Min Hu1,2, Jun Yao1,2, Li Cai3, Bachman, Kurt E.4, van den Brûle, Frédéric5, Velculescu, Victor6, Polyak, Kornelia1,2 KorneliaPolyak@dfci.harvard.edu
Publikováno v:
Nature Genetics. Aug2005, Vol. 37 Issue 8, p899-905. 7p.
Autor:
Esashi, Fumiko1, Christ, Nicole2, Gannon, Julian1, Yilun Liu1, Hunt, Tim1, Jasin, Maria2, West, Stephen C.1 stephen.west@cancer.org.uk
Publikováno v:
Nature. 3/31/2005, Vol. 434 Issue 7033, p598-604. 7p.
Autor:
Susanna Koivuluoma, Sandra Vorimo, Tiina M. Mattila, Anna Tervasmäki, Timo Kumpula, Outi Kuismin, Robert Winqvist, Jukka Moilanen, Tuomo Mantere, Katri Pylkäs
TINF2 is a critical subunit of the shelterin complex, which protects and maintains the length of telomeres. Pathogenic missense and truncating TINF2 mutations are causative for dyskeratosis congenita (DC), a rare, dominantly inherited bone marrow fai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f82ca51eaee43bed77387d88cb2876ed
http://urn.fi/urn:nbn:fi-fe2023053150756
http://urn.fi/urn:nbn:fi-fe2023053150756
Autor:
Hege Edvarsen, Ana Lluch, Antonio Falcó, Laura J. van't Veer, Carlos Lozano-Asencio, Allan Balmain, Anne Lise Børresen-Dale, Joan Climent, Raimundo Cervera-Vidal, Vita Fedele, Rafa Tabares-Seisdedos, Irene Tadeo-Cervera, Sten Cornelissen, Jaume Forés-Martos, Julia Sierra-Roca, Marjanka Schmidt, Vessela N. Kristensen, Pilar Eroles, David A. Quigley
Publikováno v:
CEU Repositorio Institucional
Fundación Universitaria San Pablo CEU (FUSPCEU)
npj Breast Cancer, Vol 7, Iss 1, Pp 1-12 (2021)
NPJ breast cancer, vol 7, iss 1
Fundación Universitaria San Pablo CEU (FUSPCEU)
npj Breast Cancer, Vol 7, Iss 1, Pp 1-12 (2021)
NPJ breast cancer, vol 7, iss 1
Polymorphisms in the PER3 gene have been associated with several human disease phenotypes, including sleep disorders and cancer. In particular, the long allele of a variable number of tandem repeat (VNTR) polymorphism has been previously linked to an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe28842d1952d5013093a97ab6d336f5
https://doi.org/10.1038/s41523-021-00329-2
https://doi.org/10.1038/s41523-021-00329-2
Autor:
Walker, John M., Brooks, Susan A., Harris, Adrian, Jeffery, Rosemary, Hunt, Toby, Poulsom, Richard
Publikováno v:
Breast Cancer Research Protocols; 2006, p323-346, 24p
Publikováno v:
Breast Cancer Research Protocols; 2006, p347-362, 16p
Publikováno v:
Breast Cancer Research Protocols; 2006, p309-322, 14p
Autor:
Walker, John M., Brooks, Susan A., Harris, Adrian, Blancato, Jan K., Williams, Mary Steele, Dickson, Robert B.
Publikováno v:
Breast Cancer Research Protocols; 2006, p297-307, 11p
Publikováno v:
Breast Cancer Research Protocols; 2006, p269-295, 27p