Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Mei Lin Z. Bissonnette"'
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 10 (2023)
Background: Nontargeted renal biopsy is essential to diagnosis, classification, and prognostication of medical renal disease. Inadequate biopsies delay diagnosis, expose the patient to repeated biopsy, and increase costs. Objective: The purpose of th
Externí odkaz:
https://doaj.org/article/eb264d123aa946679cf897c6cd1eb10e
Autor:
David D. M. Nicholl, MD, MS, John P. Whitelaw, MD, Rene V. Weir, MD, Mei Lin Z. Bissonnette, MD, PhD, John S. Gill, MD, MS, David N. Landsberg, MD
Publikováno v:
Transplantation Direct, Vol 7, Iss 12, p e790 (2021)
Externí odkaz:
https://doaj.org/article/6d46201dbb774c73a710ead21dfc13a5
Publikováno v:
Kidney International Reports, Vol 2, Iss 3, Pp 493-497 (2017)
Externí odkaz:
https://doaj.org/article/56f0b4da2e53436e9bf493a7e8446256
Autor:
Samuel L. Volchenboum, Stephen X. Skapek, James R. Anderson, Douglas S. Hawkins, Frederic G. Barr, Julie M. Gastier-Foster, Michele R. Wing, Timothy J. Triche, David M. Parham, Aliya N. Husain, Mei Lin Z. Bissonnette, Karen M. Bachmeyer, Ling Teng, Raphael A. Wilson
The clinical application of complex molecular classifiers as diagnostic or prognostic tools has been limited by the time and cost needed to apply them to patients. Using an existing 50-gene expression signature known to separate two molecular subtype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e1b3d2934e5aa00d26e463be717a990
https://doi.org/10.1158/0008-5472.c.6504642.v1
https://doi.org/10.1158/0008-5472.c.6504642.v1
Autor:
Samuel L. Volchenboum, Stephen X. Skapek, James R. Anderson, Douglas S. Hawkins, Frederic G. Barr, Julie M. Gastier-Foster, Michele R. Wing, Timothy J. Triche, David M. Parham, Aliya N. Husain, Mei Lin Z. Bissonnette, Karen M. Bachmeyer, Ling Teng, Raphael A. Wilson
PDF file - 714K, Supplementary Figure 1 Two-gene combinations from the 50-gene F1/F2 classifier with >98% classification efficiency in the Williamson data set. Supplementary Figure 2 Thirteen two-gene combinations with >99% classification efficiency,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fdbdf8498929e01b9913a9cb4d0de6f
https://doi.org/10.1158/0008-5472.22396725
https://doi.org/10.1158/0008-5472.22396725
Autor:
Cahyani Gita Ambarsari, Rachel A. Annunziato, Evamaria Anvari, Carlos E. Araya, Rossella Attini, Rose Mary Ayoob, Justine Bacchetta, Rossana Baracco, Joanne M. Bargman, Antonio Bellasi, Ezequiel Bellorin-Font, William M. Bennett, Scott Bieber, Mei Lin Z. Bissonnette, Geoffrey A. Block, Brendan Bowman, Patrick D. Brophy, Deborah J. Brouwer-Maier, Steven Brunelli, David Bushinsky, Jonathan Casavant, Roberta Cerutti, Vimal Chadha, Christopher T. Chan, Bipan Chand, Deepa H. Chand, Anthony Chang, Chaim Charytan, Joline L.T. Chen, Wei Chen, Andrew I. Chin, Yeoungjee Cho, William R. Clark, John H. Crabtree, Daniel Cukor, Serpil Muge Deger, Lucia Del Vecchio, Alonso R. Diaz, Stephanie L. Donahue, Ramanath Dukkipati, Claire Dunphy, Mohamed Elbokl, Fabrizio Fabrizi, Mohammed K. Faizan, Steven Fishbane, Molly Fisher, William Henry Fissell, Jorge Ignacio Fonseca-Correa, Bethany J. Foster, Seth B. Furgeson, Ashley M. Gefen, Guido Gembillo, F. John Gennari, Marc Ghannoum, Griet Glorieux, Sharlene Anuska Greenwood, Dieter Haffner, Rainer Himmele, Jean L. Holley, Daljit K. Hothi, T. Alp Ikizler, Sarbjit Vanita Jassal, Kirsten L. Johansen, David W. Johnson, Kamyar Kalantar-Zadeh, Pranay Kathuria, Irfan Khan, Paul L. Kimmel, Alan S. Kliger, Timothy Koh Jee Kam, Berfu Korucu, Pelagia Koufaki, Eugene C. Kovalik, Robin A. Kremsdorf, Martin Kreuzer, Mahesh Krishnan, Martin K. Kuhlmann, Danica Lam, Yu-Chi Lapid, Francesco Locatelli, Joseph B. Lockridge, Charmaine E. Lok, Etienne Macedo, John D. Mahan, Harold J. Manley, Kevin J. Martin, Nicola Matthews, Juliet Mayes, Ian E. McCoy, Christopher W. Mcintyre, Rajnish Mehrotra, Ravindra L. Mehta, Mark M. Mitsnefes, Michele H. Mokrzycki, Bogdan Momciu, Liz Mooney, Alvin H. Moss, Vinay Narasimha Krishna, Sharon J. Nessim, Allen R. Nissenson, Vandana Dua Niyyar, Ali Olyaei, Alejandra Orozco-Guillén, David I. Ortiz-Melo, Biff F. Palmer, Suetonia C. Palmer, Patrick S. Parfrey, Jeffery Perl, Giorgina B. Piccoli, Joanne D. Pittard, Connie M. Rhee, Ezequiel Ridruejo, Claudio Rigatto, Matthew B. Rivara, Darren M. Roberts, AnnaMarie Rodriguez, Mariano Rodriguez, Rudolph A. Rodriguez, Claudio Ronco, Mitchell H. Rosner, John H. Sadler, Valeria Saglimbene, Fabio R. Salerno, Domenico Santoro, Franz Schaefer, Christine B. Sethna, Hitesh H. Shah, Jenny I. Shen, Jeffrey Silberzweig, Rossella Siligato, Pamela S. Singer, Michael J.G. Somers, null Soo, Bruce Spinowitz, Deborah Stein, Emily Stonebrook, Giovanni F.M. Strippoli, Cheuk-Chun Szeto, Isaac Teitelbaum, Rebecca Thomas-Chen, Ashita J. Tolwani, Massimo Torreggiani, Avram Z. Traum, Luis G. Tulloch-Palomino, Tushar J. Vachharajani, Rudolph P. Valentini, Peter Noel Van Buren, René G. VanDeVoorde, Raymond Vanholder, Thanh-Mai Vo, Bradley A. Warady, Adam Weinstein, Katherine Wesseling-Perry, James B. Wetmore, Mark E. Williams, Jay B. Wish, Joshua J. Zaritsky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72a1da8126fc9020044e15338151d9c7
https://doi.org/10.1016/b978-0-323-79135-9.09989-4
https://doi.org/10.1016/b978-0-323-79135-9.09989-4
Publikováno v:
Journal of the American Society of Nephrology.
Autor:
A. Wayne Vogl, Alvin Ka-Wai Wong, Kelly M. McNagny, Ido Refaeli, Mei Lin Z. Bissonnette, Calvin D. Roskelley, Michael R. Hughes, Sean J. Barbour, Benjamin S. Freedman
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Scientific Reports
Scientific Reports
Dominant and recessive mutations in podocalyxin (PODXL) are associated with human kidney disease. Interestingly, some PODXL mutations manifest as anuria while others are associated with proteinuric kidney disease. PODXL heterozygosity is associated w
Autor:
Avi Z. Rosenberg, Kuang-Yu Jen, Vighnesh Walavalkar, Anatoly Urisman, Jonathan E. Zuckerman, Mei Lin Z. Bissonnette, David E. Manthey, Darshana Govind, Pinaki Sarder, Avinash Kammardi Shashiprakash, Brandon Ginley, Brendon Lutnick, John E. Tomaszewski, Nicholas Lucarelli, Marco Delsante
Publikováno v:
Proc SPIE Int Soc Opt Eng
Histologic examination of interstitial fibrosis and tubular atrophy (IFTA) is critical to determine the extent of irreversible kidney injury in renal disease. The current clinical standard involves pathologist's visual assessment of IFTA, which is pr