Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 4

Results: 18

Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 553, doi. 10.1007/s10689-014-9733-4

By:

Ponti, G.;
Pellacani, G.;
Ruini, C.;
Percesepe, A.;
Longo, C.;
Mandel, V.;
Crucianelli, F.;
Gorelli, G.;
Tomasi, A.

Publication type:

Article

Cribriform-morular variant of papillary thyroid carcinoma: an indication to screen for occult FAP.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 547, doi. 10.1007/s10689-014-9732-5

By:

Levy, Rachel;
Hui, Vanessa;
Sood, Rupa;
Fish, Stephanie;
Markowitz, Arnold;
Wong, Richard;
Guillem, José

Publication type:

Article

Association of interleukin-23 receptor gene polymorphisms with risk of bladder cancer in Chinese.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 619, doi. 10.1007/s10689-014-9731-6

By:

Tang, Tielong;
Xue, Hui;
Cui, Shu;
Gong, Zhiyong;
Fei, Zhonghai;
Cheng, Shulin;
Gui, Chunyan

Publication type:

Article

Genetic 135G/C polymorphism of RAD51 gene and risk of cancer: a meta-analysis of 28,956 cases and 28,372 controls.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 515, doi. 10.1007/s10689-014-9729-0

By:

Zhang, Bei-bei;
Wang, Dao-gang;
Xuan, Chao;
Sun, Gui-li;
Deng, Kai-feng

Publication type:

Article

Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 583, doi. 10.1007/s10689-014-9730-7

By:

Árvai, Kristóf;
Horváth, Péter;
Balla, Bernadett;
Tőkés, Anna;
Tobiás, Bálint;
Takács, István;
Nagy, Zsolt;
Lakatos, Péter;
Kósa, János

Publication type:

Article

'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.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 625, doi. 10.1007/s10689-014-9734-3

By:

Bancroft, Elizabeth;
Castro, Elena;
Ardern-Jones, Audrey;
Moynihan, Clare;
Page, Elizabeth;
Taylor, Natalie;
Eeles, Rosalind;
Rowley, Emma;
Cox, Karen

Publication type:

Article

Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 637, doi. 10.1007/s10689-014-9735-2

By:

Menko, Fred;
Maher, Eamonn;
Schmidt, Laura;
Middelton, Lindsay;
Aittomäki, Kristiina;
Tomlinson, Ian;
Richard, Stéphane;
Linehan, W.

Publication type:

Article

Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 645, doi. 10.1007/s10689-014-9736-1

By:

Ávila, Alexandre;
Krepischi, Ana;
Moredo, Luciana;
Aguiar, Talita;
Silva, Felipe;
Sá, Bianca;
Nóbrega, Amanda;
Achatz, Maria;
Duprat, João;
Landman, Gilles;
Carraro, Dirce

Publication type:

Article

A primary care audit of familial risk in patients with a personal history of breast cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 591, doi. 10.1007/s10689-014-9737-0

By:

Nathan, Paul;
Ahluwalia, Aneeta;
Chorley, Wendy

Publication type:

Article

A polymorphism at miRNA-122-binding site in the IL-1α 3′UTR is associated with risk of epithelial ovarian cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 595, doi. 10.1007/s10689-014-9739-y

By:

Zhang, Zhu;
Zhou, Bin;
Gao, Qianqian;
Wu, Yuke;
Zhang, Kui;
Pu, Yan;
Song, Yaping;
Zhang, Lin;
Xi, Mingrong

Publication type:

Article

Phenotype of SDHB mutation carriers in the Netherlands.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 651, doi. 10.1007/s10689-014-9738-z

By:

Hulsteijn, Leonie;
Niemeijer, Nienke;
Hes, Frederik;
Bayley, Jean-Pierre;
Tops, Carli;
Jansen, Jeroen;
Corssmit, Eleonora

Publication type:

Article

High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 603, doi. 10.1007/s10689-014-9740-5

By:

Riahi, Aouatef;
Kharrat, Maher;
Lariani, Imen;
Chaabouni-Bouhamed, Habiba

Publication type:

Article

Molecular heterogeneity of familial myeloproliferative neoplasms revealed by analysis of the commonly acquired JAK2, CALR and MPL mutations.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 659, doi. 10.1007/s10689-014-9743-2

By:

Langabeer, Stephen;
Haslam, Karl;
Linders, Jennifer;
Percy, Melanie;
Conneally, Eibhlin;
Hayat, Amjad;
Hennessy, Brian;
Leahy, Maeve;
Murphy, Karen;
Murray, Margaret;
Ni Ainle, Fionnuala;
Thornton, Patrick;
Sargent, Jeremy

Publication type:

Article

Association of reduced XRCC2 expression with lymph node metastasis in breast cancer tissues.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 611, doi. 10.1007/s10689-014-9745-0

By:

Bashir, Nabiha;
Sana, Syeda;
Mahjabeen, Ishrat;
Kayani, Mahmood

Publication type:

Article

Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 527, doi. 10.1007/s10689-014-9741-4

By:

Selkirk, Christina;
Vogel, Kristen;
Newlin, Anna;
Weissman, Scott;
Weiss, Shelly;
Wang, Chi-Hsiung;
Hulick, Peter

Publication type:

Article

The secondary bile acid, deoxycholate accelerates intestinal adenoma-adenocarcinoma sequence in Apc mice through enhancing Wnt signaling.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 563, doi. 10.1007/s10689-014-9742-3

By:

Cao, Hailong;
Luo, Shenhui;
Xu, Mengque;
Zhang, Yujie;
Song, Shuli;
Wang, Shan;
Kong, Xinyue;
He, Nana;
Cao, Xiaocang;
Yan, Fang;
Wang, Bangmao

Publication type:

Article

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 573, doi. 10.1007/s10689-014-9744-1

By:

Rosty, Christophe;
Walsh, Michael;
Lindor, Noralane;
Thibodeau, Stephen;
Mundt, Erin;
Gallinger, Steven;
Aronson, Melyssa;
Pollett, Aaron;
Baron, John;
Pearson, Sally;
Clendenning, Mark;
Walters, Rhiannon;
Nagler, Belinda;
Crawford, William;
Young, Joanne;
Winship, Ingrid;
Win, Aung;
Hopper, John;
Jenkins, Mark;
Buchanan, Daniel

Publication type:

Article

Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 4, p. 537, doi. 10.1007/s10689-014-9728-1

By:

Jönsson, Jenny-Maria;
Bartuma, Katarina;
Dominguez-Valentin, Mev;
Harbst, Katja;
Ketabi, Zohreh;
Malander, Susanne;
Jönsson, Mats;
Carneiro, Ana;
Måsbäck, Anna;
Jönsson, Göran;
Nilbert, Mef

Publication type:

Article