Zobrazeno 1 - 10
of 888
pro vyhledávání: '"M, Rowley"'
Autor:
Margaret Phillips, Jason B. Reed, Dave Zwicky, Amy S. van Epps, Amy G. Buhler, Erin M. Rowley, Qianjin Zhang, James M. Cox, Wei Zakharov
Publikováno v:
IEEE Access, Vol 12, Pp 62648-62663 (2024)
A systematic review is a specialized type of literature review used to collect and synthesize all the available evidence related to a research question. The methods for systematic reviews should be transparent and reproducible so that other researche
Externí odkaz:
https://doaj.org/article/badcffba781b4c9dbb9783d08aa176e3
Autor:
Belle W. X. Lim, Na Li, Simone M. Rowley, Ella R. Thompson, Simone McInerny, Magnus Zethoven, Rodney J. Scott, Lisa Devereux, Erica K. Sloan, Paul A. James, Ian G. Campbell
Publikováno v:
npj Breast Cancer, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract While protein-truncating variants in RAD51C have been shown to predispose to triple-negative (TN) breast cancer (BC) and ovarian cancer, little is known about the pathogenicity of missense (MS) variants. The frequency of rare RAD51C MS varia
Externí odkaz:
https://doaj.org/article/cb1b85b7941943879757906ddef2dd42
Autor:
Na Li, Belle W. X. Lim, Ella R. Thompson, Simone McInerny, Magnus Zethoven, Dane Cheasley, Simone M. Rowley, Michelle W. Wong-Brown, Lisa Devereux, Kylie L. Gorringe, Erica K. Sloan, Alison Trainer, Rodney J. Scott, Paul A. James, Ian G. Campbell
Publikováno v:
npj Breast Cancer, Vol 7, Iss 1, Pp 1-8 (2021)
Abstract Breast cancer (BC) has a significant heritable component but the genetic contribution remains unresolved in the majority of high-risk BC families. This study aims to investigate the monogenic causes underlying the familial aggregation of BC
Externí odkaz:
https://doaj.org/article/91c2f977e91949a284425595f07cfa53
Autor:
Sally M. Hunter, Genevieve V. Dall, Maria A. Doyle, Richard Lupat, Jason Li, Prue Allan, Simone M. Rowley, David Bowtell, On behalf of AOCS, Ian G. Campbell, Kylie L. Gorringe
Publikováno v:
BMC Research Notes, Vol 13, Iss 1, Pp 1-8 (2020)
Abstract Objective Ovarian fibromas and adenofibromas are rare ovarian tumours. They are benign tumours composed of spindle-like stromal cells (pure fibroma) or a mixture of fibroblast and epithelial components (adenofibroma). We have previously show
Externí odkaz:
https://doaj.org/article/b04951423f094474882d7f56bebcc2fa
Autor:
Deepak N. Subramanian, Magnus Zethoven, Simone McInerny, James A. Morgan, Simone M. Rowley, Jue Er Amanda Lee, Na Li, Kylie L. Gorringe, Paul A. James, Ian G. Campbell
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Around half of the heritability underpinning familial high-grade serous ovarian carcinoma remains unidentified. Here, the authors show that extremely rare protein encoding loss-of-function variants, with a high degree of genetic heterogeneity, may ac
Externí odkaz:
https://doaj.org/article/a521a39eb0dc4d439f6807027b6fe81f
Autor:
Dane Cheasley, Matthew J. Wakefield, Georgina L. Ryland, Prue E. Allan, Kathryn Alsop, Kaushalya C. Amarasinghe, Sumitra Ananda, Michael S. Anglesio, George Au-Yeung, Maret Böhm, David D. L. Bowtell, Alison Brand, Georgia Chenevix-Trench, Michael Christie, Yoke-Eng Chiew, Michael Churchman, Anna DeFazio, Renee Demeo, Rhiannon Dudley, Nicole Fairweather, Clare G. Fedele, Sian Fereday, Stephen B. Fox, C Blake Gilks, Charlie Gourley, Neville F. Hacker, Alison M. Hadley, Joy Hendley, Gwo-Yaw Ho, Siobhan Hughes, David G. Hunstman, Sally M. Hunter, Tom W. Jobling, Kimberly R. Kalli, Scott H. Kaufmann, Catherine J. Kennedy, Martin Köbel, Cecile Le Page, Jason Li, Richard Lupat, Orla M. McNally, Jessica N. McAlpine, Anne-Marie Mes-Masson, Linda Mileshkin, Diane M. Provencher, Jan Pyman, Kurosh Rahimi, Simone M. Rowley, Carolina Salazar, Goli Samimi, Hugo Saunders, Timothy Semple, Ragwha Sharma, Alice J. Sharpe, Andrew N. Stephens, Niko Thio, Michelle C. Torres, Nadia Traficante, Zhongyue Xing, Magnus Zethoven, Yoland C. Antill, Clare L. Scott, Ian G. Campbell, Kylie L. Gorringe
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Whether mucinous ovarian carcinoma (MOC) arises from cells at the ovary or from metastases from other primary sites is an unanswered question. Here, Cheasley et al perform a genetic analysis of the disease, showing that MOC arises at the ovary.
Externí odkaz:
https://doaj.org/article/9047c1d475514bf5becaaddcde7c44d4
Autor:
Na Li, Simone M. Rowley, Ella R. Thompson, Simone McInerny, Lisa Devereux, Kaushalya C. Amarasinghe, Magnus Zethoven, Richard Lupat, David Goode, Jason Li, Alison H. Trainer, Kylie L. Gorringe, Paul A. James, Ian G. Campbell
Publikováno v:
Breast Cancer Research, Vol 20, Iss 1, Pp 1-11 (2018)
Abstract Background Genome-wide association studies (GWASs) have identified numerous single-nucleotide polymorphisms (SNPs) associated with small increases in breast cancer risk. Studies to date suggest that some SNPs alter the expression of the asso
Externí odkaz:
https://doaj.org/article/87e91e02038b476ca773dac090bf25d6
Autor:
Ella R. Thompson, Michelle Wong-Brown, Simone M. Rowley, Susan Dooley, Na Lil, Michael Hipwell, Simone McInerny, Cliff Meldrum, Lisa Devereux, David Mossman, Alison H. Trainer, Briar-Rose Millar, Gillian Mitchell, Cate Smith, Paul A. James, Ian G. Campbell, Rodney J. Scott, Katarzyna Klonowska, Anna Jakubowska, Jelena Maksimenko, Arvids Irmejs, Miki Nakazawa-Miklasevica, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, Edvins Miklasevics, Karolina Tęcza, Jolanta Pamuła-Piłat, Joanna Łanuszewska, Ewa Grzybowska, M. Szwiec, J. Tomiczek-Szwiec, M. Gełej, C. Cybulski, T. Huzarski, E. Kilar, Małgorzata Oczko-Wojciechowska, Michał Świerniak, Jolanta Krajewska, Małgorzata Kowalska, Tomasz Tyszkiewicz, Agnieszka Pawlaczek, Michał Jarząb, Monika Kowal, Dagmara Rusinek, Jadwiga Zebracka-Gala, Agnieszka Czarniecka, Barbara Jarzab, Andrzej Plawski, Paweł Borun, Joanna Szczepinska, Monika Siolek, Beata Kozak-Klonowska, Katarzyna Kaczmarek, Magdalena Muszyńska, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Jan Lubiński, Michał Post
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss S1, Pp 1-5 (2017)
Externí odkaz:
https://doaj.org/article/959ca802658e4fe59a0522035180cc7e
Autor:
Eric S. Johnson, John F. Dickerson, William M. Vollmer, Alee M. Rowley, Cheryl Ritenbaugh, Richard A. Deyo, Lynn DeBar
Publikováno v:
BMC Medical Research Methodology, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background Propensity scores are typically applied in retrospective cohort studies. We describe the feasibility of matching on a propensity score derived from a retrospective cohort and subsequently applied in a prospective cohort study of p
Externí odkaz:
https://doaj.org/article/1f84437fd97643cdadaadabcd6f89c13
Autor:
Peter J. Fuller, Ian G. Campbell, Kaushalya C. Amarasinghe, Colin J.R. Stewart, Dilys T.H. Leung, Simon Chu, Simone M. Rowley, Maria Alexiadis
S1. Total number of mutated genes identified within this study that are also mutated in the studies of Caburet et al [21], Zehir et al [22], Kandoth et al [23], Lawrence et al [24] and Nik-Zainal et al [25]. Genes mutated in this current study are al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79aa950abca3ea074e9925dd4bad6a94
https://doi.org/10.1158/1541-7786.22516048.v1
https://doi.org/10.1158/1541-7786.22516048.v1
