Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 1

Results: 23

Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 157, doi. 10.1007/s10689-014-9763-y

By:

Huq, Aamira;
Kentwell, Maira;
Tirimacco, Amanda;
Rossini, Jacqueline;
Rawlings, Lesley;
Winship, Ingrid

Publication type:

Article

Single nucleotide polymorphisms in PDCD6 gene are associated with the development of cervical squamous cell carcinoma.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 1, doi. 10.1007/s10689-014-9767-7

By:

Zhou, Bin;
Bai, Peng;
Xue, Hui;
Zhang, Zhu;
Shi, Shaoqing;
Zhang, Kui;
Wang, Yanyun;
Wang, Kana;
Quan, Yi;
Song, Yaping;
Zhang, Lin

Publication type:

Article

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 145, doi. 10.1007/s10689-014-9748-x

By:

Bogdanova, Natalia;
Togo, Alexandr;
Ratajska, Magdalena;
Kluźniak, Wojtek;
Takhirova, Zalina;
Tarp, Theresa;
Prokofyeva, Darya;
Bermisheva, Marina;
Yanus, Grigoriy;
Gorodnova, Tatiana;
Sokolenko, Anna;
Kuźniacka, Alina;
Podolak, Amira;
Stukan, Maciej;
Wokołorczyk, Dominika;
Gronwald, Jacek;
Vasilevska, Danuta;
Rudaitis, Vilius;
Runnebaum, Ingo;
Dürst, Matthias

Publication type:

Article

Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 129, doi. 10.1007/s10689-014-9747-y

By:

Ahlborn, Lise;
Steffensen, Ane;
Jønson, Lars;
Djursby, Malene;
Nielsen, Finn;
Gerdes, Anne-Marie;
Hansen, Thomas

Publication type:

Article

Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 9, doi. 10.1007/s10689-014-9749-9

By:

Guan, Yanfang;
Hu, Hong;
Peng, Yin;
Gong, Yuhua;
Yi, Yuting;
Shao, Libin;
Liu, Tengfei;
Li, Gairui;
Wang, Rongjiao;
Dai, Pingping;
Bignon, Yves-Jean;
Xiao, Zhe;
Yang, Ling;
Mu, Feng;
Xiao, Liang;
Xie, Zeming;
Yan, Wenhui;
Xu, Nan;
Zhou, Dongxian;
Yi, Xin

Publication type:

Article

Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 89, doi. 10.1007/s10689-014-9764-x

By:

Vogelaar, Ingrid;
Post, Rachel;
Vosse, Esther;
Krieken, J.;
Hoogerbrugge, Nicoline;
Ligtenberg, Marjolijn;
Gómez García, Encarna

Publication type:

Article

APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 41, doi. 10.1007/s10689-014-9750-3

By:

Quadri, Marialuisa;
Vetro, Annalisa;
Gismondi, Viviana;
Marabelli, Monica;
Bertario, Lucio;
Sala, Paola;
Varesco, Liliana;
Zuffardi, Orsetta;
Ranzani, Guglielmina

Publication type:

Article

Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 61, doi. 10.1007/s10689-014-9751-2

By:

Shia, Jinru;
Stadler, Zsofia;
Weiser, Martin;
Vakiani, Efsevia;
Mendelsohn, Robin;
Markowitz, Arnold;
Shike, Moshe;
Boland, C.;
Klimstra, David

Publication type:

Article

Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 151, doi. 10.1007/s10689-014-9752-1

By:

Mann, Kirsty;
Magee, Jill;
Guillaud-Bataille, Marine;
Blondel, Christophe;
Bressac-de Paillerets, Brigitte;
Yeatman, Josie;
Winship, Ingrid

Publication type:

Article

MLH1 promotor hypermethylation does not rule out a diagnosis of Lynch syndrome: a case report.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 77, doi. 10.1007/s10689-014-9753-0

By:

Raymond, Victoria;
Morris, Arden;
Hafez, Khaled;
Greenson, Joel

Publication type:

Article

Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li-Fraumeni syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 161, doi. 10.1007/s10689-014-9754-z

By:

Etzold, Anna;
Schröder, Julia;
Bartsch, Oliver;
Zechner, Ulrich;
Galetzka, Danuta

Publication type:

Article

Familial and sporadic pancreatic cancer share the same molecular pathogenesis.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 95, doi. 10.1007/s10689-014-9755-y

By:

Norris, Alexis;
Roberts, Nicholas;
Jones, Siân;
Wheelan, Sarah;
Papadopoulos, Nickolas;
Vogelstein, Bert;
Kinzler, Kenneth;
Hruban, Ralph;
Klein, Alison;
Eshleman, James

Publication type:

Article

Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 167, doi. 10.1007/s10689-014-9756-x

By:

Gustafson, Shanna;
Raymond, Victoria;
Marvin, Monica;
Else, Tobias;
Koeppe, Erika;
Stoffel, Elena;
Everett, Jessica

Publication type:

Article

Mitochondrial membrane potential and reactive oxygen species in cancer stem cells.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 19, doi. 10.1007/s10689-014-9757-9

By:

Zhang, Bei-bei;
Wang, Dao-gang;
Guo, Fen-fen;
Xuan, Chao

Publication type:

Article

Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 105, doi. 10.1007/s10689-014-9759-7

By:

Heiniger, Louise;
Butow, Phyllis;
Coll, Joseph;
Bullen, Tracey;
Wilson, Judy;
Baylock, Brandi;
Meiser, Bettina;
Price, Melanie

Publication type:

Article

Desmoid tumour in familial adenomatous polyposis patients: responses to treatments.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 31, doi. 10.1007/s10689-014-9760-1

By:

Desurmont, Thibault;
Lefèvre, Jérémie;
Shields, Conor;
Colas, Chrystelle;
Tiret, Emmanuel;
Parc, Yann

Publication type:

Article

The impact of risk-reducing gynaecological surgery in premenopausal women at high risk of endometrial and ovarian cancer due to Lynch syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 51, doi. 10.1007/s10689-014-9761-0

By:

Moldovan, Ramona;
Keating, Sianan;
Clancy, Tara

Publication type:

Article

Down-regulation of malignant potential by alpha linolenic acid in human and mouse colon cancer cells.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 25, doi. 10.1007/s10689-014-9762-z

By:

Chamberland, John;
Moon, Hyun-Seuk

Publication type:

Article

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 69, doi. 10.1007/s10689-014-9765-9

By:

Connor, Ashton;
Katzov-Eckert, Hagit;
Whelan, Thomas;
Aronson, Melyssa;
Lau, Lynette;
Marshall, Christian;
Charames, George;
Pollett, Aaron;
Gallinger, Steven;
Lerner-Ellis, Jordan

Publication type:

Article

Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 117, doi. 10.1007/s10689-014-9766-8

By:

Berrino, Jacopo;
Berrino, Franco;
Francisci, Silvia;
Peissel, Bernard;
Azzollini, Jacopo;
Pensotti, Valeria;
Radice, Paolo;
Pasanisi, Patrizia;
Manoukian, Siranoush

Publication type:

Article

Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 135, doi. 10.1007/s10689-014-9769-5

By:

Rahman, Belinda;
Meisel, Susanne;
Fraser, Lindsay;
Side, Lucy;
Gessler, Sue;
Wardle, Jane;
Lanceley, Anne

Publication type:

Article

18th annual meeting: Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC).

Published in:: Familial Cancer, 2015, v. 14, n. 1, p. 175, doi. 10.1007/s10689-014-9768-6
Publication type:: Article

Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women.

Published in:

Familial Cancer, 2015, v. 14, n. 1, p. 81, doi. 10.1007/s10689-014-9746-z

By:

Smolarz, Beata;
Makowska, Marianna;
Samulak, Dariusz;
Michalska, Magdalena;
Romanowicz, Hanna

Publication type:

Article