Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Douglas Levine"'
Autor:
Tara Coffin, Deborah Bowen, Elizabeth Swisher, Karen Lu, Nadine Rayes, Barbara Norquist, Stephanie Blank, Douglas Levine, Jamie Bakkum-Gamez, Gini Fleming, Olufunmilayo Olopade, Alan D’Andrea, Denise Nebgen, Christine Peterson, Mark Munsell, Kathleen Gavin, Rebecca Lechner, Jamie Crase, Deborah Polinsky, Iris Romero
Publikováno v:
JMIR Formative Research, Vol 6, Iss 10, p e34055 (2022)
BackgroundGenetic testing uptake is low, despite the well-established connection between pathogenic variants in certain cancer-linked susceptibility genes and ovarian cancer risk. Given that most major insurers cover genetic testing for those with a
Externí odkaz:
https://doaj.org/article/042f974a27c04a5bb441e72675ede81d
Autor:
Irina Tunnage, Olivia Lara, Selim Misirlioglu, Luiza Doro Pereira, Suhaib Abdelrahman, Douglas Levine, Kari Hacker
Publikováno v:
Gynecologic Oncology. 166:S132-S133
Autor:
Tara Coffin, Deborah Bowen, Elizabeth Swisher, Karen Lu, Nadine Rayes, Barbara Norquist, Stephanie Blank, Douglas Levine, Jamie Bakkum-Gamez, Gini Fleming, Olufunmilayo Olopade, Alan D’Andrea, Denise Nebgen, Christine Peterson, Mark Munsell, Kathleen Gavin, Rebecca Lechner, Jamie Crase, Deborah Polinsky, Iris Romero
Publikováno v:
JMIR formative research. 6(10)
BackgroundGenetic testing uptake is low, despite the well-established connection between pathogenic variants in certain cancer-linked susceptibility genes and ovarian cancer risk. Given that most major insurers cover genetic testing for those with a
Autor:
Tara Coffin, Deborah Bowen, Elizabeth Swisher, Karen Lu, Nadine Rayes, Barbara Norquist, Stephanie Blank, Douglas Levine, Jamie Bakkum-Gamez, Gini Fleming, Olofunmi Olopade, Alan D’Andrea, Denise Nebgen, Christine Peterson, Mark Munsell, Kathleen Gavin, Rebecca Lechner, Jamie Crase, Deborah Polinsky, Iris Romero
BACKGROUND Genetic testing uptake is low, despite the well-established connection between pathogenic variants in certain cancer-linked susceptibility genes and ovarian cancer risk. Given that most major insurers cover genetic testing for those with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10e141dc88747e91ed25ab617be2dd6b
https://doi.org/10.2196/preprints.34055
https://doi.org/10.2196/preprints.34055
Autor:
Benjamin King, Elke Van Oudenhove, Selim Misirlioglu, Ernesto Arostegui Fernandez, Douglas Levine, Timothee Lionnet
Publikováno v:
Cancer Research. 79:3780-3780
Ovarian cancer is the leading cause of mortality among gynecological malignancies; 70% of patients who initially respond to therapy eventually relapse and die. Within highly heterogeneous tumors, resistance originates from a small number of cells tha
Autor:
Ed, Dicks, Honglin, Song, Susan J, Ramus, Elke Van, Oudenhove, Jonathan P, Tyrer, Maria P, Intermaggio, Siddhartha, Kar, Patricia, Harrington, David D, Bowtell, Aocs Study, Group, Mine S, Cicek, Julie M, Cunningham, Brooke L, Fridley, Jennifer, Alsop, Mercedes, Jimenez-Linan, Anna, Piskorz, Teodora, Goranova, Emma, Kent, Nadeem, Siddiqui, James, Paul, Robin, Crawford, Samantha, Poblete, Shashi, Lele, Lara, Sucheston-Campbell, Kirsten B, Moysich, Weiva, Sieh, Valerie, McGuire, Jenny, Lester, Kunle, Odunsi, Alice S, Whittemore, Natalia, Bogdanova, Matthias, Dürst, Peter, Hillemanns, Beth Y, Karlan, Aleksandra, Gentry-Maharaj, Usha, Menon, Marc, Tischkowitz, Douglas, Levine, James D, Brenton, Thilo, Dörk, Ellen L, Goode, Simon A, Gayther, D P Paul, Pharoah
Publikováno v:
Oncotarget
We analyzed whole exome sequencing data in germline DNA from 412 high grade serous ovarian cancer (HGSOC) cases from The Cancer Genome Atlas Project and identified 5,517 genes harboring a predicted deleterious germline coding mutation in at least one
Autor:
Robert Holt, José Sebastião Dos Santos, Andrew Mungall, Matthew Meyerson, Marco Marra, Giovanni Ciriello, Piotr Mieczkowski, John Weinstein, Cristovam Scapulatempo-Neto, Katherine Hoadley, Henrique Silveira, Gordon Mills, Matthew Anderson, Kin Chan, Sahil Seth, Stephen Benz, Zigui Chen, Matthew H. Bailey, Joshua Stuart, Juan Emmanuel Martinez Ledesma, Leng Han, Tiandao Li, Jay Bowen, Douglas Levine, Dmitry Gordenin, Charles Perou, Roy Tarnuzzer, Ken Chen, Jurandyr Andrade, MICHAEL MCLELLAN, Steven Jones, Daniel Tiezzi, SOPHIA WANG, Clement Adebamowo, David Heiman
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Cervical cancer remains one of the leading causes of cancer-related deaths worldwide. Here we report the extensive molecular characterization of 228 primary cervical cancers, one of the largest comprehensive genomic studies of cervical cancer to date
Autor:
Weiva Sieh, Gerhard Coetzee, Paul James, Lambertus Kiemeney, Susanne Kjaer, Iain McNeish, Diana M Eccles, Jolanta Kupryjanczyk, Arif Ekici, Dennis Hazelett, Claus Høgdall, Iwona Krystyna Rzepecka, Allan Jensen, Melissa Southey, Camilla Krakstad, Graham Giles, Usha Menon, Thilo Dörk, Alvaro Monteiro, Kate Lawrenson, Ronny Drapkin, Diether Lambrechts, Douglas Levine, Rosalind Glasspool, Anna Jakubowska, Yin Ling Woo, Florian Heitz, Robert Vierkant, Suhn Rhie, Liisa Pelttari, Georgia Chenevix-Trench, Agnieszka Dansonka-Mieszkowska, Simon Gert Coetzee, Soo Teo, Jolanta Lissowska, Susan Ramus, Keitaro Matsuo, Keren Levanon, Jan Lubinski, Alexander Hein
Publikováno v:
Human Molecular Genetics, 24, 13, pp. 3595-607
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Human Molecular Genetics, 24, 3595-607
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Human Molecular Genetics, 24, 3595-607
Contains fulltext : 154725.pdf (Publisher’s version ) (Closed access) Understanding the regulatory landscape of the human genome is a central question in complex trait genetics. Most single-nucleotide polymorphisms (SNPs) associated with cancer ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee887b3c4645a469def8ed3424464a1c
https://europepmc.org/articles/PMC4459387/
https://europepmc.org/articles/PMC4459387/
Publikováno v:
The American Journal of Gastroenterology. 101:1964-1971
It has been suggested that patients with Barrett's esophagus (BE) are unusually resistant to the antisecretory effects of proton pump inhibitors (PPIs).To compare intragastric and intraesophageal acidity in patients with BE receiving esomeprazole 40
Publikováno v:
Clinical Therapeutics. 23:660-679
Background: Acid peptic disease is a common problem, with a similar prevalence of gastroesophageal reflux disease (GERD) in adults and children. The presentation of GERD in infants and children varies from crying, irritability, or sleep disturbance t