Zobrazeno 1 - 10
of 20
pro vyhledávání: '"J P, Struewing"'
Autor:
J. P. Struewing, Christopher I. Amos
Publikováno v:
Cancer. 71:566-572
Aside from age, family history is the strongest predictor of ovarian cancer risk. Genetic components of risk for ovarian cancer have been evaluated by a number of designs, including case-control studies of family history and other risk factors, segre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0540dd96f12d82ecccc512e388172209
https://doi.org/10.1002/cncr.2820710212
https://doi.org/10.1002/cncr.2820710212
Autor:
Barbara Marinelli, Mohammad Hedayati, Lawrence Grossman, Donato Calista, M. T. Landi, P Minghetti, T Tseng, Benedetta Albetti, Giorgio Landi, Andrea A. Baccarelli, J P Struewing
Publikováno v:
British Journal of Cancer
We recently reported an association between low DNA repair capacity, measured through the host-cell reactivation assay, and melanoma risk in subjects with dysplastic naevi or low tanning ability. We investigated the genetic basis for these findings b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0671d06edf5717f7bdff70273f1097
https://doi.org/10.1038/sj.bjc.6601385
https://doi.org/10.1038/sj.bjc.6601385
Autor:
Eitan Friedman, R. Gershoni, J. P. Struewing, Angela Chetrit, Flora Lubin, Rizel S, Baruch Modan, Tamar Peretz, G Hirsh-Yechezkel
Publikováno v:
Gynecologic Oncology. 89:494-498
Objective The objective was to evaluate the prevalence of BRCA1/2 mutations in selected categories of ovarian cancer patients in Israel. Methods Blood samples and specimens of ovarian tumors were obtained in the course of a national case control stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8917ef75d30d67dabecf2e42655f594a
https://doi.org/10.1016/s0090-8258(03)00152-5
https://doi.org/10.1016/s0090-8258(03)00152-5
Publikováno v:
British Journal of Cancer
One of the most common melanoma-related CDKN2A mutations reported in North America is the V126D mutation. We examined nine markers surrounding CDKN2A in three American and four Canadian families carrying the V126D mutation. All seven families had a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8edd704702374e296eb935f1b7321b40
https://doi.org/10.1054/bjoc.2001.1944
https://doi.org/10.1054/bjoc.2001.1944
Autor:
Chen-Yang Shen, Show Lin Yang, Bolot Kalmyrzaev, Michael F. Press, Dong Young Noh, Leslie Bernstein, Elaine A. Ostrander, Giske Ursin, Sei Hyun Ahn, J. P. Struewing, Annika Lindblom, Brian E. Henderson, Eric Karlins, Douglas F. Easton, Robert Luben, Kerstin B. Meyer, Radhika Prathalingam, Kathleen E. Malone, Carlos Caldas, Christopher A. Haiman, Ana-Teresa Maia, Miriam S. Udler, Ed Dicks, Radka Platte, Keun-Young Yoo, Anna H. Wu, Alison M. Dunning, Paul D.P. Pharoah, David R. Doody, Bruce A.J. Ponder, Loic Le Marchand, Catherine S. Healey, Chia-Ni Hsiung, Laurence K. Kolonel, Sara Margolin, Erika M. Kwon, Stewart McArthur, Helen I. Field, Jinghui Zhang, Andrew E. Teschendorff, Jonathan Tyrer, Daehee Kang, Melanie Maranian, Shahana Ahmed
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics; Vol 19
Human Molecular Genetics; Vol 19
Recent genome-wide association studies have identified a breast cancer susceptibility locus on 16q12 with an unknown biological basis. We used a set of single nucleotide polymorphism (SNP) markers to generate a fine-scale map and narrowed the region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e754287347b330e09fe7be4a62ffa2
https://pubmed.ncbi.nlm.nih.gov/20332101
https://pubmed.ncbi.nlm.nih.gov/20332101
Autor:
Dale L. Preston, Alice J. Sigurdson, Laura Bowen, Michael Hauptmann, Parveen Bhatti, Bruce H. Alexander, J. P. Struewing, Marvin Rosenstein, Michele M. Doody, Robert M. Weinstock, Steven L. Simon, Preetha Rajaraman, Marilyn Stovall, Martha S. Linet
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 16(10)
Background: Although genes involved in apoptosis pathways and DNA repair pathways are both essential for maintaining genomic integrity, genetic variants in DNA repair have been thought to increase susceptibility to radiation carcinogenesis, but simil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0171aada3901267dd6066b4ced120e9
https://pubmed.ncbi.nlm.nih.gov/17932347
https://pubmed.ncbi.nlm.nih.gov/17932347
Autor:
T Wagner, Kenneth Offit, Katherine L. Nathanson, Peter Devilee, Janet E. Olson, Ilyushik E, Lenka Foretova, Jacek Gronwald, Pascaline Berthet, Muhammad Usman Rashid, Isabelle Coupier, Noralane M. Lindor, T A Sellers, Alfons Meindl, Dieter Schaefer, Shirley Hodgson, Beatrix Versmold, Olufunmilayo I. Olopade, Susan M. Domchek, Christoph Engel, Olga M. Sinilnikova, Vernon S. Pankratz, Gail E. Tomlinson, David J. Hughes, Amanda B. Spurdle, Horst J, Jakub Lubiński, Maaike P.G. Vreeswijk, Gordon Glendon, Robert A. Vierkant, Francine Durocher, Frédéric Guénard, Henry T. Lynch, Douglas F. Easton, Mary B. Daly, Susan Peock, Åke Borg, Jacques Simard, Heli Nevanlinna, Georgia Chenevix-Trench, Irene L. Andrulis, M. Cook, Caroline Baynes, Steven A. Narod, Judy Garber, Mark H. Greene, J. N. Weitzel, Patrick J. Morrison, Anna Jakubowska, Johanna Tommiska, Kristiina Aittomäki, Hans F. A. Vasen, Claudine Isaacs, Csilla Szabo, Dominique Stoppa-Lyonnet, Fergus J. Couch, Michal Zikan, Backenhorn K, Christian Sutter, Diana Torres, Antonis C. Antoniou, Ute Hamann, Andrew K. Godwin, kConFab, Rita K. Schmutzler, Tomas Kirchhoff, Susan L. Neuhausen, Zachary S. Fredericksen, Agnès Hardouin, Timothy R. Rebbeck, J. P. Struewing, Mary Porteous
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 16(7)
The AURKA oncogene is associated with abnormal chromosome segregation and aneuploidy and predisposition to cancer. Amplification of AURKA has been detected at higher frequency in tumors from BRCA1 and BRCA2 mutation carriers than in sporadic breast t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e729af1ad692c81d0912e36f2eca59e
https://pubmed.ncbi.nlm.nih.gov/18006949
https://pubmed.ncbi.nlm.nih.gov/18006949
Publikováno v:
Epidemiology (Cambridge, Mass.). 14(6)
SUMMARY BACKGROUND Over-expression of the human epidermal growth factor receptor 2 (Her2) protooncogene is associated with poor prognosis among female patients with breast cancer. A polymorphism in the HER2 gene (I655V) has been associated with an el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfa322ed0109a8f6346f45548288c49
https://pubmed.ncbi.nlm.nih.gov/14569185
https://pubmed.ncbi.nlm.nih.gov/14569185
Autor:
M. Altaras, J. P. Struewing, Angela Chetrit, Y. Fishler, Giulia Barda, Baruch Modan, Flora Lubin, Siegal Sadetzki, Hanoch Levavi, Joseph Menczer
Publikováno v:
Gynecologic oncology. 88(1)
Objective. The aim of the present study was to compare demographic and clinical characteristics of primary peritoneal carcinoma (PPC) to ovarian carcinoma (OvC) with regard to BRCA mutation frequencies. Methods. Incident cases of histologically confi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::259c36e4052c214a80d5c38288bf4bfc
https://pubmed.ncbi.nlm.nih.gov/12504628
https://pubmed.ncbi.nlm.nih.gov/12504628
Autor:
W W, Wang, A B, Spurdle, P, Kolachana, B, Bove, B, Modan, S M, Ebbers, G, Suthers, M A, Tucker, D J, Kaufman, M M, Doody, R E, Tarone, M, Daly, H, Levavi, H, Pierce, A, Chetrit, G H, Yechezkel, G, Chenevix-Trench, K, Offit, A K, Godwin, J P, Struewing
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 10(9)
RAD51 colocalizes with both BRCA1 and BRCA2, and genetic variants in RAD51 would be candidate BRCA1/2 modifiers. We searched for RAD51 polymorphisms by sequencing 20 individuals. We compared the polymorphism allele frequencies between female BRCA1/2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d60b7f47dcf4011b01c27402f923a557
https://pubmed.ncbi.nlm.nih.gov/11535547
https://pubmed.ncbi.nlm.nih.gov/11535547