Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Anita Iyer"'
Autor:
Amy Mueller, Karen Gutekunst, Tamsen Dunn, Leonard Buchner, Anita Iyer, Margaret Porter, Kristen Meier, Nitin Udar, Paul Wenz, Diane Ward, Jing Lu, Aaron Wise, Shannon E. Smith, Robert Haigis, Shivani Dhillon
Publikováno v:
The Journal of Molecular Diagnostics. 22:159-178
A next-generation sequencing method was developed that can distinguish single-stranded modifications from low-frequency somatic mutations present on both strands of DNA in formalin-fixed paraffin-embedded colorectal cancer samples. We applied this me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5b86adf344d4ac70b97169b4389bc64
https://doi.org/10.1016/j.jmoldx.2019.09.009
https://doi.org/10.1016/j.jmoldx.2019.09.009
Autor:
Ashwin Siva Das, Anita Iyer
Publikováno v:
Pathology. 54:S59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::237d3176988cca1db04aca04fabd935a
https://doi.org/10.1016/j.pathol.2021.12.193
https://doi.org/10.1016/j.pathol.2021.12.193
Publikováno v:
Pathology. 54:S59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0df7aafb1ad6ebefbf0f43b4c0fc8725
https://doi.org/10.1016/j.pathol.2021.12.192
https://doi.org/10.1016/j.pathol.2021.12.192
Publikováno v:
ANZ Journal of Surgery. 90:1789-1790
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a087e8e46d2a0faaf24684153bb71229
https://doi.org/10.1111/ans.15654
https://doi.org/10.1111/ans.15654
Autor:
Yu Jiang, Serena Lei, Marina Bibikova, Tamsen Dunn, Michael Strömberg, Han-Yu Chuang, Anita Iyer, Gwenn Berry, Dorothea Emig-Agius, Justin Robbins, Marc Peeters, Nitin Udar, Brandy Klotzle, Michael Dickover, Jeffrey M. Hegarty
Publikováno v:
Bioinformatics
MotivationNext-Generation Sequencing (NGS) technology is transitioning quickly from research labs to clinical settings. The diagnosis and treatment selection for many acquired and autosomal conditions necessitate a method for accurately detecting som
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8aee66f8d8c76e618daf3f9f30ce1e1
http://europepmc.org/articles/PMC6499249
http://europepmc.org/articles/PMC6499249
Autor:
Sarennya Pathmanandavel, Winston Liauw, Peter Colligan, Ashleigh Splitt, Marie Ranson, Martin G Carolan, Kara L. Vine, Nicholas G Hirst, Morteza Aghmesheh, Anita Iyer, Martin Illemann, Alistair Lochhead, Therese M. Becker, Daniel Brungs
Publikováno v:
Pathology. 51(5)
Gastroesophageal adenocarcinoma is a common and highly lethal malignancy. Cancer stem cells (CSCs) have a key role in the development and progression of metastatic disease. While expression of CSC markers CD44, CD133 and aldehyde dehydrogenase 1 (ALD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac71a1d070c3f2e3bfa2cdebaf6814d
https://pubmed.ncbi.nlm.nih.gov/31230819
https://pubmed.ncbi.nlm.nih.gov/31230819
Publikováno v:
Pathology. 52:S83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8b958794d80ab6856bb62000a8160a
https://doi.org/10.1016/j.pathol.2020.01.275
https://doi.org/10.1016/j.pathol.2020.01.275
Autor:
Anita Iyer, Ryan Slaughter, Jean-Yves Douillard, Darcy Vavrek, A. Scott Jung, Nitin Udar, Jun Dong, Catherine Lofton-Day, Karen Gutekunst, Bruce A. Bach, Kristen Meier, Marc Peeters
Publikováno v:
Journal of cancer research and clinical oncology
Journal of Cancer Research and Clinical Oncology
Journal of Cancer Research and Clinical Oncology
Purpose To validate a next-generation sequencing (NGS)-based companion diagnostic using the MiSeqDx® sequencing instrument to simultaneously detect 56 RAS mutations in DNA extracted from formalin-fixed paraffin-embedded metastatic colorectal cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::849065961b4de090dd012b24055b5e29
https://hdl.handle.net/10067/1547670151162165141
https://hdl.handle.net/10067/1547670151162165141
Autor:
Michael Strömberg, Dorothea Emig-Agius, Anita Iyer, Nitin Udar, Yu Jiang, Tamsen Dunn, Gwenn Berry
Publikováno v:
BCB
A method for robustly and accurately detecting rare DNA mutations in tumor samples is critical to cancer research. Because many clinical tissue repositories have only FFPE-degraded tumor samples, and no matched normal sample from healthy tissue avail
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38cc61d0ab6e712b58f34b199df0a99c
https://doi.org/10.1145/3107411.3108203
https://doi.org/10.1145/3107411.3108203
