Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jennifer Stroop"'
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2021)
Familial paraganglioma syndrome type 1 (PGL-1) is maternally imprinted, caused by SDHD mutations on the paternally inherited allele, and presents with paragangliomas and pheochromocytomas that are usually benign. We describe a kindred with a germline
Externí odkaz:
https://doaj.org/article/510ab0e933104103ab53e456e83aa191
Publikováno v:
Molecular Carcinogenesis. 51:647-658
Lynch syndrome (LS) is caused by germline mutations in DNA mismatch repair (MMR) genes. MMR recognizes and repairs DNA mismatches and small insertion/deletion loops. Carriers of MMR gene variants have a high risk of developing colorectal, endometrial
Publikováno v:
Surgical Oncology Clinics of North America. 18:53-71
Screening for genetic abnormalities is a relatively complex task requiring detailed training and knowledge. Analysis of a person's genetic makeup has implications not only for that individual but also for their progenitors, offspring, siblings, and s
Autor:
Jennifer Stroop
Publikováno v:
Pediatric Annals. 29:279-282
Because of the significant impact [that] genetic susceptibility information may have on disease management and prevention, it is vitally important that the public, health professionals and administrators become educated regarding the importance of th
Autor:
Giselle K. Perez, Robert M. Greenstein, Dean G. Cruess, Stacy Cruess, Jennifer Stroop, R C Schwartz, Molly Brewer
Publikováno v:
Journal of health communication. 16(6)
Genetic testing for the breast cancer genes 1/2 (BRCA 1/2) has helped women determine their risk of developing breast and ovarian cancer. As interest in genetic testing has grown, companies have created strategies to disseminate information about tes
Autor:
Benoit Panzini, Niki Boyd, Cathy Gilpin, Sam S. Yoon, Sonya Zaor, Daniel Fontaine, Sylviane Olschwang, Sarah M. Nikkel, Jane Green, Carla Oliveira, Maria Ana Redal, Daniel G. Coit, Gregory Y. Lauwers, Lori Van Manen, David G. Huntsman, Pardeep Kaurah, Debrah Wirtzfeld, Paul D.P. Pharoah, Wendy S. Rubinstein, Jennifer Stroop, Antonio Pizzuti, Alessandro De Luca, Andrée MacMillan, Janine Senz, James M. Ford, Bridget A. Fernandez, Marc S. Greenblatt, Steven Gallinger, Carlos A. Vaccaro, Robert M. Greenstein, Daniel C. Chung, Wendy McKinnon, Scott M. Weissman, Courtney Sebold, Mary Connolly-Wilson, Marc Tischkowitz, Henry T. Lynch, Gianpaolo Suriano, Nicki Chun, Dwight Yim
ContextHereditary diffuse gastric cancer is caused by germline mutations in the epithelial cadherin (CDH1) gene and is characterized by an increased risk for diffuse gastric cancer and lobular breast cancer.ObjectiveTo determine whether recurring ger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f732fdbdb7380430fbb258a8fb011312
http://hdl.handle.net/11573/366499
http://hdl.handle.net/11573/366499