Issue 4/2014
Content (18 Articles)
Genetic 135G/C polymorphism of RAD51 gene and risk of cancer: a meta-analysis of 28,956 cases and 28,372 controls
Bei-bei Zhang, Dao-gang Wang, Chao Xuan, Gui-li Sun, Kai-feng Deng
Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice
Christina G. Selkirk, Kristen J. Vogel, Anna C. Newlin, Scott M. Weissman, Shelly M. Weiss, Chi-Hsiung Wang, Peter J. Hulick
Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome
Jenny-Maria Jönsson, Katarina Bartuma, Mev Dominguez-Valentin, Katja Harbst, Zohreh Ketabi, Susanne Malander, Mats Jönsson, Ana Carneiro, Anna Måsbäck, Göran Jönsson, Mef Nilbert
Cribriform-morular variant of papillary thyroid carcinoma: an indication to screen for occult FAP
Rachel A. Levy, Vanessa W. Hui, Rupa Sood, Stephanie Fish, Arnold J. Markowitz, Richard J. Wong, José G. Guillem
Muir–Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients
G. Ponti, G. Pellacani, C. Ruini, A. Percesepe, C. Longo, V. Desmond Mandel, F. Crucianelli, G. Gorelli, A. Tomasi
The secondary bile acid, deoxycholate accelerates intestinal adenoma–adenocarcinoma sequence in Apc min/+ mice through enhancing Wnt signaling
Hailong Cao, Shenhui Luo, Mengque Xu, Yujie Zhang, Shuli Song, Shan Wang, Xinyue Kong, Nana He, Xiaocang Cao, Fang Yan, Bangmao Wang
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
Christophe Rosty, Michael D. Walsh, Noralane M. Lindor, Stephen N. Thibodeau, Erin Mundt, Steven Gallinger, Melyssa Aronson, Aaron Pollett, John A. Baron, Sally Pearson, Mark Clendenning, Rhiannon J. Walters, Belinda N. Nagler, William J. Crawford, Joanne P. Young, Ingrid Winship, Aung Ko Win, John L. Hopper, Mark A. Jenkins, Daniel D. Buchanan
Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples
Kristóf Árvai, Péter Horváth, Bernadett Balla, Anna M. Tőkés, Bálint Tobiás, István Takács, Zsolt Nagy, Péter Lakatos, János P. Kósa
A primary care audit of familial risk in patients with a personal history of breast cancer
Paul Nathan, Aneeta Ahluwalia, Wendy Chorley
A polymorphism at miRNA-122-binding site in the IL-1α 3′UTR is associated with risk of epithelial ovarian cancer
Zhu Zhang, Bin Zhou, Qianqian Gao, Yuke Wu, Kui Zhang, Yan Pu, Yaping Song, Lin Zhang, Mingrong Xi
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families
Aouatef Riahi, Maher Kharrat, Imen Lariani, Habiba Chaabouni-Bouhamed
Association of reduced XRCC2 expression with lymph node metastasis in breast cancer tissues
Nabiha Bashir, Syeda Sana, Ishrat Mahjabeen, Mahmood Akhtar Kayani
Association of interleukin-23 receptor gene polymorphisms with risk of bladder cancer in Chinese
Tielong Tang, Hui Xue, Shu Cui, Zhiyong Gong, Zhonghai Fei, Shulin Cheng, Chunyan Gui
“It’s all very well reading the letters in the genome, but it’s a long way to being able to write”: Men’s interpretations of undergoing genetic profiling to determine future risk of prostate cancer
Elizabeth K. Bancroft, Elena Castro, Audrey Ardern-Jones, Clare Moynihan, Elizabeth Page, Natalie Taylor, Rosalind A. Eeles, Emma Rowley, Karen Cox
Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment
Fred H. Menko, Eamonn R. Maher, Laura S. Schmidt, Lindsay A. Middelton, Kristiina Aittomäki, Ian Tomlinson, Stéphane Richard, W. Marston Linehan
Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma
Alexandre Leon Ribeiro de Ávila, Ana Cristina Victorino Krepischi, Luciana Facure Moredo, Talita Ferreira Marques Aguiar, Felipe Carneiro da Silva, Bianca Costa Soares de Sá, Amanda França de Nóbrega, Maria Isabel Waddington Achatz, João Pedreira Duprat, Gilles Landman, Dirce Maria Carraro
Phenotype of SDHB mutation carriers in the Netherlands
Leonie T. van Hulsteijn, Nienke D. Niemeijer, Frederik J. Hes, Jean-Pierre Bayley, Carli M. Tops, Jeroen C. Jansen, Eleonora P. M. Corssmit
Molecular heterogeneity of familial myeloproliferative neoplasms revealed by analysis of the commonly acquired JAK2, CALR and MPL mutations
Stephen E. Langabeer, Karl Haslam, Jennifer Linders, Melanie J. Percy, Eibhlin Conneally, Amjad Hayat, Brian Hennessy, Maeve Leahy, Karen Murphy, Margaret Murray, Fionnuala Ni Ainle, Patrick Thornton, Jeremy Sargent