Zobrazeno 31 - 40
of 483
pro vyhledávání: '"Albert de la Chapelle"'
Autor:
Albert de la Chapelle, Gary Reid, Jeffrey Bell, Luis Vaccarello, George Lewandowski, Jeffrey Fowler, Lynne Eaton, Larry Copeland, David E. Cohn, Patti Dunn, Janet Lombardi, Pamela Penzone, Mark Clendenning, Thomas W. Prior, Judith A. Westman, Hidewaki Nakagawa, Jennifer La Jeunesse, Ilene Comeras, Daniel Fix, Kaisa Sotamaa, Janet Lockman, Jenny Panescu, Wendy Frankel, Heather Hampel
Endometrial cancer is the most common cancer in women with Lynch syndrome. The identification of individuals with Lynch syndrome is desirable because they can benefit from increased cancer surveillance. The purpose of this study was to determine the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a91e8ac3166f8d33fb2e210382bbf136
https://doi.org/10.1158/0008-5472.c.6494682
https://doi.org/10.1158/0008-5472.c.6494682
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03a312ce5bd2554b5b8aa100e29f6b73
https://doi.org/10.1158/0008-5472.22370685.v1
https://doi.org/10.1158/0008-5472.22370685.v1
Supplementary Table 1 from A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
Autor:
Albert de la Chapelle, Juha Kere, Saul Suster, Wei Li, Hong Jiao, Sandya Liyanarachchi, Rebecca Nagy, Huiling He
Supplementary Table 1 from A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b602976f528ee44940441ae4f54bcaa1
https://doi.org/10.1158/0008-5472.22377546
https://doi.org/10.1158/0008-5472.22377546
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Figure 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e21b3ce9f79af67b38f086b2d56f94f
https://doi.org/10.1158/0008-5472.22370688.v1
https://doi.org/10.1158/0008-5472.22370688.v1
Supplementary Table 3 from A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
Autor:
Albert de la Chapelle, Juha Kere, Saul Suster, Wei Li, Hong Jiao, Sandya Liyanarachchi, Rebecca Nagy, Huiling He
Supplementary Table 3 from A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ad65a3f47e0470c5edc3f72360c12f7
https://doi.org/10.1158/0008-5472.22377540.v1
https://doi.org/10.1158/0008-5472.22377540.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 2 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35983558639f12401ff99760e775b25
https://doi.org/10.1158/0008-5472.22370682.v1
https://doi.org/10.1158/0008-5472.22370682.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Large germline deletions within the mismatch repair gene MSH2 account for a significant proportion (up to 20%) of all deleterious mutations of this gene which are associated with Lynch syndrome. An exons 1 to 6 deletion of MSH2, originally reported i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c191f3329d9a72241f6091604193cc13
https://doi.org/10.1158/0008-5472.c.6496491.v1
https://doi.org/10.1158/0008-5472.c.6496491.v1
Autor:
Brian H. Shirts, Peter G. Shields, Dan Jones, Lori Nelsen, Sameer Mahesh, Jo L. Freudenheim, Shyamal Bastola, Kisa Weeman, Yinong Liu, Electra D. Paskett, Esther H. Rehmus, Matthew F. Kalady, Wendy L. Frankel, Jeffrey Zangmeister, Paul J. Goodfellow, Brandie Heald, Christopher Bigley, Mitchell Haut, Shelly Cummings, Kristin Miller, Mark Arnold, Sharon Cole, Chaoyang Li, Albert de la Chapelle, Ian M. Paquette, Weiqiang Zhao, Rachel Pearlman, Ahmet Yilmaz, Filix Kencana, Heather Hampel, Peter P. Stanich, Albert Malcolm, Thomas W. Prior, Richard M. Goldberg, Joanna M. Brell, David J Draper, Aruna Gowda, Jason Bacher, Charles Bane, Ilene Lattimer, Angela Jacobson, Colin C. Pritchard, Benjamin Swanson
Publikováno v:
JCO Precis Oncol
PURPOSE Hereditary cancer syndromes infer high cancer risks and require intensive surveillance. Identification of high-risk individuals among patients with colorectal cancer (CRC) needs improvement. METHODS Three thousand three hundred ten unselected
Autor:
W. G. Li, Matthew D. Ringel, Sandya Liyanarachchi, Pearlly S. Yan, Albert de la Chapelle, Daniel F. Comiskey, Huiling He, Ralf Bundschuh, Altan M. Turkoglu, Pamela Brock
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports
Scientific Reports
Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer. The molecular characteristics of histologically normal appearing tissue adjacent to the tumor (NAT) from PTC patients are not well characterized. The aim of this study was t
Autor:
Adrian A. Suarez, Albert de la Chapelle, Weiqiang Zhao, Colin C. Pritchard, David E. Cohn, Paul J. Goodfellow, Ritu Salani, Larry J. Copeland, Ahmet Yilmaz, Joseph P. McElroy, David M. O'Malley, Floor J. Backes, Heather Hampel, Dan Jones, Casey Cosgrove, Jeffrey M. Fowler, Wei Chen, Rachel Pearlman, Peter P. Stanich, Wendy L. Frankel
Publikováno v:
Gynecol Oncol
Objective Lynch syndrome is the most common cause of inherited endometrial cancer, attributable to germline pathogenic variants (PV) in mismatch repair (MMR) genes. Tumor microsatellite instability (MSI-high) and MMR IHC abnormalities are characteris