Zobrazeno 1 - 10 of 179 pro vyhledávání: '"Kathleen, Buckley"'
1
Akademický článek
Theory‐based behavior change intervention to increase uptake of risk‐reducing salpingo‐oophorectomy in women with a BRCA1 or BRCA2 pathogenic variant: The PREVENT randomized controlled trial
Autor: Kelly A. Metcalfe, Tuya Pal, Steven A. Narod, Susan Armel, Salma Shickh, Kathleen Buckley, Scott T. Walters, Sarah Brennenstuhl, Anita Y. Kinney
Publikováno v: Cancer Medicine, Vol 12, Iss 17, Pp 18246-18257 (2023)
Abstract Objective To evaluate the effect of a theory‐based behavioral intervention delivered by genetic counselors on the uptake of risk‐reducing salpingo‐oophorectomy (RRSO) at 12 and 24 months by women with a BRCA1 or BRCA2 pathogenic varian
Externí odkaz: https://doaj.org/article/3d630fad647649d8b2ca75d271b70fb0
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2
Akademický článek
Incidental findings from cancer next generation sequencing panels
Autor: Nika Maani, Karen Panabaker, Jeanna M. McCuaig, Kathleen Buckley, Kara Semotiuk, Kirsten M. Farncombe, Peter Ainsworth, Seema Panchal, Bekim Sadikovic, Susan Randall Armel, Hanxin Lin, Raymond H. Kim
Publikováno v: npj Genomic Medicine, Vol 6, Iss 1, Pp 1-7 (2021)
Abstract Next-generation sequencing (NGS) technologies have facilitated multi-gene panel (MGP) testing to detect germline DNA variants in hereditary cancer patients. This sensitive technique can uncover unexpected, non-germline incidental findings in
Externí odkaz: https://doaj.org/article/51d40d0aa8aa4187b039858a26fe2992
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4
Lessons Learned Using Logic Models to Design and Guide DNP Projects
Autor: Susan Gorschboth, Debra Bingham, Brenda Windemuth, Margaret Hammersla, Susan L. Bindon, Shannon Idzik, Kathleen Buckley
Publikováno v: Nurse Educator. 46:E127-E131
BACKGROUND A final culminating project that is derived from a practice immersion experience is a critical part of a doctor of nursing practice (DNP) program. PROBLEM Many schools use well-designed quality improvement (QI) projects to meet this requir
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7609690b6d4010570cb24b8392db2267
https://doi.org/10.1097/nne.0000000000001025
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5
Incidental findings from cancer next generation sequencing panels
Autor: Karen Panabaker, Nika Maani, Jeanna McCuaig, Peter Ainsworth, Hanxin Lin, Kathleen Buckley, Kara Semotiuk, Seema Panchal, Bekim Sadikovic, Raymond H. Kim, Susan Armel, Kirsten M. Farncombe
Publikováno v: npj Genomic Medicine, Vol 6, Iss 1, Pp 1-7 (2021)
Paediatrics Publications
NPJ Genomic Medicine
Next-generation sequencing (NGS) technologies have facilitated multi-gene panel (MGP) testing to detect germline DNA variants in hereditary cancer patients. This sensitive technique can uncover unexpected, non-germline incidental findings indicative
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd6dcdecc8ee7aba550e59dd9839b33c
https://doi.org/10.1038/s41525-021-00224-6
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6
Using Simulation to Improve Communication Skills in Nurse Practitioner Preceptors
Autor: Linda Aveni Murray, Kathleen Buckley
Publikováno v: Journal for Nurses in Professional Development. 33:33-39
Role transitions in nursing may lead to stress and anxiety or the novice, which can be decreased with appropriate mentoring by preceptors. However, preceptors commonly describe having a lack of mentoring skills. This project focused on nurse practiti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd7965562ac4b4819ae33a0e4368d514
https://doi.org/10.1097/nnd.0000000000000325
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7
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)
Autor: Matthew S. Lebo, Kathleen-Rose Zakoor, Kathy Chun, Marsha D. Speevak, John S. Waye, Elizabeth McCready, Jillian S. Parboosingh, Ryan E. Lamont, Harriet Feilotter, Ian Bosdet, Tracy Tucker, Sean Young, Aly Karsan, George S. Charames, Ronald Agatep, Elizabeth L. Spriggs, Caitlin Chisholm, Nasim Vasli, Hussein Daoud, Olga Jarinova, Robert Tomaszewski, Stacey Hume, Sherryl Taylor, Mohammad R. Akbari, Jordan Lerner-Ellis, Ron Agatep, Peter Ainsworth, Melyssa Aronson, Raveen Basran, Andre Blavier, Andrea Blumenthal, Kym Boycott, Michael Brudno, Kathleen Buckley, Jodi Campbell, Philippe M. Campeau, Melanie Care, Nancy Carson, Ronald Carter, George Charames, David Chitayat, George Chong, Edmond Chouinard, Kenneth J. Craddock, Rod Docking, Andrea Eisen, Hanna Faghfoury, Sandra Farrell, Bridget Fernandez, Marc Fiume, Cynthia Forster-Gibson, Jan Friedman, William Foulkes, Peter Goodhand, Jessica Gu, Robert Hegele, Spring Holter, Sheri Horsburgh, Lauren Hughes, Franny Jewett, Anne Junker, Sam Khalouei, Joan Knoll, Elena Kolomeitz, Bartha Knoppers, Ryan Lamont, Matthew Lebo, Georges Maire, Christian Marshall, Grant Mitchell, Michael J Moorhouse, Chantal Morel, Tanya Nelson, Abdul Noor, Brian O'Connor, Darren O'Rielly, Francis Ouellette, Jillian Parboosingh, Hilary Racher, Peter Ray, Heidi Rehm, Christie Riddell, Jean-Baptiste Riviere, David S. Rosenblatt, Guy Rouleau, Andrea Ruchon, Peter Sabatini, Bekim Sadikovic, Kara Semotiuk, Stephen W. Scherer, Cheryl Shuman, Josh Silver, Katherine Siminovitch, Lesley Solomon-Izsak, Jean-Francois Soucy, Marsha Speevak, James Stavropoulos, Lincoln Stein, Rhonda Tannenbaum, Deborah Terespolsky, Richard F. Wintle, Beatrix Wong, Nora Wong, Marina Wang, Nicholas Watkins, Shana White, Michael O. Woods, Philip Wyatt
Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics. 20(3)
PurposeThe purpose of this study was to develop a national program for Canadian diagnostic laboratories to compare DNA-variant interpretations and resolve discordant-variant classifications using the BRCA1 and BRCA2 genes as a case study.MethodsBRCA1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3af47c756c82663a6bb46ec7bc8250
https://pubmed.ncbi.nlm.nih.gov/28726806
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8
Barriers to adherence to cystic fibrosis infection control guidelines
Autor: Barbara McLurkin, Antoinette Gardner, Luis Alba, Cynthia Moodie, Paula J. Anderson, Thomas Lahiri, Terry Spencer, Mary H. Wagner, Denise B. Angst, Cindy L. Capen, Samiya Razvi, John McNamara, Mary Sachs, Henry A. Wojtczak, Catherine Kier, Monica Leupold, Donna Lindner, William M. Gershan, Manisha Desai, Ran D. Anbar, Jackie Swartz, Juyan Zhou, Kimberly Jones, Larry Gann, Yvette LeFlore, Joanna Reboul, Dana G. Kissner, Kathleen Buckley, Jerri Gray, Janet Garbarz, Thomas F. Scanlin, Daniel B. Rosenbluth, Raj Padman, Nancy N. Dambro, Ofelia Vargas-Shiraishi, Andrew J. Lipton, Mary Ellen Freeman, Elizabeth Garber, Amy Szymanski, Robert Kaslovsky, Thomas M. Murphy, Lisa Saiman, Karen McCoy, Joel H. Schmidt, Beth D'Antonio, Bettina C. Hilman, Scott A. Schroeder, Barbara T. Jansma, Rodolfo Amaro, Howard B. Panitch, David A. Hicks, Teresa Carney, Michael J. Rock, Laurie Varlotta, Jane Quante, Lynne M. Quittell, Deborah Conklin, Michael D. Cabana, Scott H. Davis, Amanda Dove, Monya Rucker
Publikováno v: Pediatric Pulmonology. 43:900-907
Background: In 2003, the American Cystic Fibrosis (CF) Foundation published revised, evidence-based guidelines for infection control. We sought to assess potential barriers to adherence to these guidelines experienced by health care professionals (HC
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f35f580d80152c938dae645abf98299
https://doi.org/10.1002/ppul.20876
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9
Colorectal cancer in a 9-year-old due to combined EPCAM and MSH2 germline mutations: case report of a unique genotype and immunophenotype
Autor: David K. Driman, Peter Ainsworth, Hector H Li-Chang, Nancy L Scanlan, Helen Levin, Kathleen Buckley, A Elizabeth Cairney, Victoria Mok Siu
Publikováno v: Journal of Clinical Pathology. 66:631-633
Lynch syndrome (LS) typically arises in the setting of a heterozygous germline mutation in one of the DNA mismatch repair (MMR) genes ( MLH1 , MSH2 , MSH6 , PMS2 ). Rarely, LS can also arise due to germline deletion of the 3′ region of the epitheli
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::281bf35f8e61f5487e6c2889e980d83e
https://doi.org/10.1136/jclinpath-2012-201376
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10
Cdc13 Delivers Separate Complexes to the Telomere for End Protection and Replication
Autor: Erin Pennock, Victoria Lundblad, Kathleen Buckley
Publikováno v: Cell. 104(3):387-396
In Saccharomyces cerevisiae, the telomere binding protein Cdc13 mediates telomere replication by recruiting telomerase, and also performs an essential function in chromosome end protection. We show here that delivery of the Stn1 protein to the telome
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::011641382139143038f4f6c564fe60be
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