Zobrazeno 1 - 10
of 39
pro vyhledávání: '"N M, Lindor"'
Autor:
Aung Ko Win, John D. Potter, Karen W. Makar, Amanda I. Phipps, Daniel D. Buchanan, John A. Baron, N. M. Lindor, Polly A. Newcomb
Publikováno v:
British Journal of Cancer
Background: Mutations in the Kirsten Ras (KRAS) oncogene are common in colorectal cancer (CRC). The role of KRAS-mutation status as a prognostic factor, however, is unclear. We evaluated the relationship between KRAS-mutation status and CRC survival,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50ecffc601a630a97e3e028cef1a4f6f
http://europepmc.org/articles/PMC3668469
http://europepmc.org/articles/PMC3668469
Autor:
Mark A. Jenkins, Daniel D. Buchanan, J. L. Hopper, N. M. Lindor, Michael Walsh, Christophe Rosty, Joanne P. Young, Mark Clendenning
Publikováno v:
Laboratory Investigation. 93:190-263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::613a0dc795b9ec862a639134c9dea16d
https://doi.org/10.1038/labinvest.2013.21
https://doi.org/10.1038/labinvest.2013.21
Autor:
Steven Gallinger, Maria Elena Martinez, N. M. Lindor, Dallas R. English, Peter T. Campbell, John L. Hopper, Graeme P. Young, Loic Le Marchand, James G. Dowty, Daniel D. Buchanan, Dennis J. Ahnen, Graham Casey, Joanne P. Young, Robert W. Haile, Misty R. Jenkins, Elizabeth T. Jacobs, Aung Ko Win, John A. Baron, S. N. Thibodeau, Polly A. Newcomb, Finlay A. Macrae, Susan Parry, John D. Potter, Ingrid Winship, Lara Lipton
Publikováno v:
British Journal of Cancer
Lynch syndrome, historically known as hereditary non-polyposis colorectal cancer (Jass, 2006), refers to colorectal and other cancers caused by germline mutations in DNA mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2 (Vasen et al, 1999). Appro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d5a7c8af7083fcff4dfb7602221e04
https://doi.org/10.1038/bjc.2011.172
https://doi.org/10.1038/bjc.2011.172
Autor:
Eric J. Bergstralh, Gloria M. Petersen, N. M. Lindor, Yanhong Wu, Lisa A. Boardman, Sandro Rossetti, Ruth A. Johnson, Stephen N. Thibodeau, Vicente E. Torres, Christina M. Heyer, Marie C. Hogan, Peter C. Harris, Mine S. Cicek, Christopher J. Ward, Jason L. Bakeberg, John R. Woollard
Publikováno v:
Human Genetics. 129:345-349
The autosomal recessive polycystic kidney disease (ARPKD) gene, PKHD1, has been implicated in the genesis or growth of colorectal adenocarcinoma, as a high level of somatic mutations was found in colorectal tumor tissue. To determine whether carriers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f554bd765ee9a7219e4a5da54833f39b
https://doi.org/10.1007/s00439-011-0950-8
https://doi.org/10.1007/s00439-011-0950-8
Autor:
M. Uhr, K. Murphy, Daniel D. Buchanan, Richard B. Halberg, Mark A. Jenkins, Pamela Ward, Jeffery W. Bacher, Louis Dubeau, Doug Storts, N. M. Lindor, James R. Eshleman, Jonas Pettersson, Eshwar B. Udho, Steve Gallinger
Publikováno v:
Annals of Oncology. 29:viii27-viii28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00143ab0a15ceb337892d871db033273
https://doi.org/10.1093/annonc/mdy269.088
https://doi.org/10.1093/annonc/mdy269.088
Autor:
Manish Gala, Stéphane Bézieau, Eric J. Jacobs, Kevin McDonnell, Amit Joshi, Leon Raskin, Shu Chen Huang, W. James Gauderman, Brian E. Henderson, Shoichiro Tsugane, Sonja I. Berndt, Marilena Melas, Jane C. Figueiredo, Christopher P. Fischer, Gregory Idos, Kana Wu, Hermann Brenner, Wei Zheng, Ulrike Peters, Stephen J. Chanock, N. M. Lindor, David J. Hunter, Martha L. Slattery, Charles Kooperberg, Cathy C. Laurie, Ben Zhang, Jing Ma, Cecelia A. Laurie, Rebecca D. Jackson, Gianluca Severi, Graham Casey, Katja Butterbach, David Van Den Berg, Frank J. Manion, Hansong Wang, Daniela Seminara, Christopher S. Carlson, Stephanie M. Gogarten, Karen W. Makar, Duncan C. Thomas, Stephen B. Gruber, David K. Levine, Barbara K. Fortini, Caroline McNeil, Flavio Lejbkowicz, Charles S. Fuchs, Motoki Iwasaki, Robert W. Haile, John D. Potter, Stephanie A. Rosse, Shuo Jiao, Keitaro Matsuo, Wei Hua Jia, Cornelia M. Ulrich, Stephanie L. Schmit, Victor Moreno, Bhramar Mukherjee, Darin Taverna, John L. Hopper, Sun Ha Jee, Dee W. West, Bette J. Caan, Andrea Z. LaCroix, Brent W. Zanke, Robert E. Schoen, Sébastien Küry, Keith R. Curtis, Loic Le Marchand, Aaron K. Aragaki, Steven Gallinger, Gad Rennert, Tabitha A. Harrison, Laurence N. Kolonel, Li Li, David V. Conti, John F. Harju, Polly A. Newcomb, David Duggan, Mathieu Lemire, Christopher K. Edlund, Thomas J. Hudson, Roger C. Green, Wei Shi, Li Hsu, Conghui Qu, Peter T. Campbell, Fredrick R. Schumacher, Mark A. Jenkins, Andrew T. Chan, Yong-Bing Xiang, Richard B. Hayes, Suminori Kono, Jenny Chang-Claude, Gerhard A. Coetzee, Carolyn M. Hutter, Hedy S. Rennert, Emily White, Graham G. Giles, Michael Hoffmeister, Xiao-Ou Shu, Edward Giovannucci
Publikováno v:
Nature Communications. 6
Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::438331cacf0732e49485debb0927a6e0
https://doi.org/10.1038/ncomms9739
https://doi.org/10.1038/ncomms9739
Autor:
Katja Butterbach, Christopher K. Edlund, Duncan C. Thomas, Gianluca Severi, Motoki Iwasaki, Keith R. Curtis, Emily White, Fredrick R. Schumacher, Wei Shi, Sun Ha Jee, W. James Gauderman, Dee W. West, Robert W. Haile, Wei Hua Jia, Jing Ma, Graham Casey, Mark A. Jenkins, Wei Zheng, Stéphane Bézieau, Mathiew Lemire, Andrea Z. LaCroix, Charles S. Fuchs, David Van Den Berg, Cecelia A. Laurie, Yong-Bing Xiang, Gad Rennert, Tabitha A. Harrison, Karen W. Makar, Marilena Melas, Hermann Brenner, Laurence N. Kolonel, Christopher S. Carlson, Cathy C. Laurie, Barbara K. Fortini, Shoichiro Tsugane, John F. Harju, Bhramar Mukherjee, Steven Gallinger, Darin Taverna, John L. Hopper, John D. Potter, Polly A. Newcomb, Aaron K. Aragaki, Sonja I. Berndt, Keitaro Matsuo, Cornelia M. Ulrich, Stephanie L. Schmit, Jane C. Figueiredo, Li Li, Victor Moreno, Eric J. Jacobs, Gregory Idos, Kana Wu, Stephen B. Gruber, Stephen J. Chanock, Kevin McDonnell, David K. Levine, Amit Joshi, Shuo Jiao, Brian E. Henderson, Thomas J. Hudson, Andrew T. Chan, Daniela Seminara, Stephanie M. Gogarten, Christopher P. Fischer, Roger C. Green, David Duggan, Bette J. Caan, Ulrike Peters, Richard B. Hayes, N. M. Lindor, Rebecca D. Jackson, David J. Hunter, Martha L. Slattery, Loic Le Marchand, Ben Zhang, Edward L. Giocannucci, Brent W. Zanke, Stephanie A. Rosse, David V. Conti, Sebastian Kury, Leon Raskin, Manish Gala, Shu Chen Huang, Frank J. Manion, Hansong Wang, Hedy S. Rennert, Gerhard A. Coetzee, Carolyn M. Hutter, Suminori Kono, Jenny Chang-Claude, Graham G. Giles, Michael Hoffmeister, Xiao-Ou Shu, Caroline McNeil, Flavio Lejbkowicz, Robert E. Schoen, Li Hsu, Conghui Qu, Peter T. Campbell, Charles Kooperberg
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
El document inclou una pàgina final amb una correcció (corrigendum). Aquesta, per si sola, té el següent DOI: 10.1038/ncomms9739 i es va publicar al mateix vol. 6.
Genetic susceptibility to colorectal cancer is caused by rare pathogenic muta
Genetic susceptibility to colorectal cancer is caused by rare pathogenic muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::275954b0a10cab2ecf3c23ec6fa97769
http://hdl.handle.net/2445/124064
http://hdl.handle.net/2445/124064
Publikováno v:
Journal of Inherited Metabolic Disease. 28:181-186
Smith-Lemli-Opitz syndrome is a rare autosomal recessive disorder characterized by multiple congenital anomalies and various degrees of cognitive deficits. This condition results from a deficiency of 7-dehydrocholesterol reductase, a critical step in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dde3a6febd4d5614da8dbc4e3daa46e
https://doi.org/10.1007/s10545-005-5515-3
https://doi.org/10.1007/s10545-005-5515-3
Autor:
Jamaica R. Robinson, N. M. Lindor, Mark A. Jenkins, Sheetal Hardikar, S. Gallinger, Xinwei Hua, Polly A. Newcomb, Graham Casey, Jonathan M. Kocarnik
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 26:439-439
Multivitamin use has been related to a modest reduced risk of colorectal cancer (CRC), but evidence on its use after diagnosis in relation to survival has been limited. Incident, invasive CRC cases were identified through cancer registries from 1997
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c98f4ba49d4bcc2201ff5917e88d735
https://doi.org/10.1158/1055-9965.epi-17-0034
https://doi.org/10.1158/1055-9965.epi-17-0034
Publikováno v:
Clinical genetics. 88(6)
Studies indicate variant of uncertain significance (VUS) results are challenging for genetic counselors and patients, often resulting in negative patient outcomes. Genetic counselors' current practices regarding VUS are unknown. This study utilized a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ecad96f9fa088fe491d9636527257275
https://pubmed.ncbi.nlm.nih.gov/25640009
https://pubmed.ncbi.nlm.nih.gov/25640009