Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Matthew A Nehs"'
Autor:
Sean M. Wrenn, Alessandra L. Moore, Hina J. Shah, Justine A. Barletta, Anand Vaidya, Kerry L. Kilbridge, Gerard M. Doherty, Heather A. Jacene, Matthew A. Nehs
Publikováno v:
The American Journal of Surgery. 225:309-314
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e159e378198bea991bd74d27bf78b450
https://doi.org/10.1016/j.amjsurg.2022.08.020
https://doi.org/10.1016/j.amjsurg.2022.08.020
Autor:
Reagan A. Collins, Catherine DiGennaro, Toni Beninato, Rajshri M. Gartland, Natalia Chaves, Jordan M. Broekhuis, Lekha Reddy, Jenna Lee, Angelina Deimiller, Maeve M. Alterio, Michael J. Campbell, Yeon Joo Lee, Tyler K. Khilnani, Latoya A. Stewart, Mollie A. O’Brien, Miguel Valdivia y Alvarado, Feibi Zheng, David McAneny, Rachel Liou, Catherine McManus, Sophie Y. Dream, Tracy S. Wang, Tina W. Yen, Amal Alhefdhi, Brendan M. Finnerty, Thomas J. Fahey, Claire E. Graves, Amanda M. Laird, Matthew A. Nehs, Frederick Thurston Drake, James A. Lee, Christopher R. McHenry, Benjamin C. James, Janice L. Pasieka, Jennifer H. Kuo, Carrie Cunningham Lubitz
Publikováno v:
Surgery, vol 173, iss 1
BackgroundThe COVID-19 pandemic profoundly impacted the delivery of care and timing of elective surgical procedures. Most endocrine-related operations were considered elective and safe to postpone, providing a unique opportunity to assess clinical ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d122aacea405d452ffd5dee33b4bc3a4
https://doi.org/10.1016/j.surg.2022.06.043
https://doi.org/10.1016/j.surg.2022.06.043
Autor:
Iñigo Landa, Erik K. Alexander, Neal I. Lindeman, Gerard M. Doherty, Jochen H. Lorch, Justine A. Barletta, Nancy L. Cho, Matthew A. Nehs, Hannah L. Johnson, Ellen Marqusee, Sara Ahmadi, Theodora Pappa
Comparison of minor allele frequencies between additional oncogenic mutations and BRAFV600E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::006742f890a8f42704fdbcd3d6868a81
https://doi.org/10.1158/1078-0432.22481505.v1
https://doi.org/10.1158/1078-0432.22481505.v1
Autor:
Eliezer M. Van Allen, Jochen H. Lorch, Rameen Beroukhim, Scott L. Carter, Levi A. Garraway, Pasi A. Janne, Tom Thomas, Erik K. Alexander, Fiona M. Fennessy, Thomas C. Lee, Travis I. Zack, Jeremiah A. Wala, Amaro Taylor-Weiner, Francis D. Moore, Matthew A. Nehs, Antonio Calles, Stefan Kraft, Glenn J. Hanna, Justine A. Barletta, Vera A. Paulson, Daniel T. Ruan, William J. Gibson
Purpose: Cancers may resist single-agent targeted therapies when the flux of cellular growth signals is shifted from one pathway to another. Blockade of multiple pathways may be necessary for effective inhibition of tumor growth. We document a case i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::058a37ff7a7629b72ba81b75a2f7eaeb
https://doi.org/10.1158/1078-0432.c.6525329
https://doi.org/10.1158/1078-0432.c.6525329
Autor:
Iñigo Landa, Erik K. Alexander, Neal I. Lindeman, Gerard M. Doherty, Jochen H. Lorch, Justine A. Barletta, Nancy L. Cho, Matthew A. Nehs, Hannah L. Johnson, Ellen Marqusee, Sara Ahmadi, Theodora Pappa
Purpose:The extent to which routine genomic sequencing can identify relevant secondary genomic alterations among BRAFV600E-mutant papillary thyroid carcinoma (PTC) is unknown. Such markers would prove highly valuable for prognostic purposes.Experimen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b68488d64e90ffc393ed2b22b5208ce
https://doi.org/10.1158/1078-0432.c.6530706.v1
https://doi.org/10.1158/1078-0432.c.6530706.v1
Autor:
Eliezer M. Van Allen, Jochen H. Lorch, Rameen Beroukhim, Scott L. Carter, Levi A. Garraway, Pasi A. Janne, Tom Thomas, Erik K. Alexander, Fiona M. Fennessy, Thomas C. Lee, Travis I. Zack, Jeremiah A. Wala, Amaro Taylor-Weiner, Francis D. Moore, Matthew A. Nehs, Antonio Calles, Stefan Kraft, Glenn J. Hanna, Justine A. Barletta, Vera A. Paulson, Daniel T. Ruan, William J. Gibson
Supplementary Figure 1 The most frequent phylogenetic tree based on sampling mutations according to their detection power (276/1000 samples). Supplementary Figure 2 Allelic copy number profiles generated by ABSOLUTE (see Methods).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::155e8f8a7642cdac128e5d0dbdc88c88
https://doi.org/10.1158/1078-0432.22463183.v1
https://doi.org/10.1158/1078-0432.22463183.v1
Autor:
Iñigo Landa, Erik K. Alexander, Neal I. Lindeman, Gerard M. Doherty, Jochen H. Lorch, Justine A. Barletta, Nancy L. Cho, Matthew A. Nehs, Hannah L. Johnson, Ellen Marqusee, Sara Ahmadi, Theodora Pappa
Comparison of clinical and pathological features of thyroid cancer patients with BRAF mutations only versus BRAF plus additional mutations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38894b1da556710cb5abdc25d75cfede
https://doi.org/10.1158/1078-0432.22481502
https://doi.org/10.1158/1078-0432.22481502
Autor:
Lauren N. Krumeich, Robert E. Roses, Lindsay E. Kuo, Brenessa M. Lindeman, Matthew A. Nehs, Ali Tavakkoli, Sareh Parangi, Richard A. Hodin, Douglas L. Fraker, Benjamin C. James, Tracy S. Wang, Carmen C. Solórzano, Carrie C. Lubitz, Heather Wachtel
Publikováno v:
Annals of Surgical Oncology. 29:2571-2579
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72485042e1a5fbce9f5b51ab641c3692
https://doi.org/10.1245/s10434-021-11192-7
https://doi.org/10.1245/s10434-021-11192-7
Autor:
Abha Aggarwal, Marie Foley Kijewski, Bixiao Zhao, Jessica A. Marshall, Jochen H. Lorch, Justine A. Barletta, Matthew A. Nehs
Publikováno v:
Surgery. 171:227-234
Anaplastic thyroid cancer is a rare but devastating malignancy. Anaplastic thyroid cancer cells exhibit the Warburg effect by preferentially undergoing glycolysis even in aerobic conditions, leading to high glucose use. Here we assess if targeted inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4069689ac4773e0bf6179f5f5cbbc1fa
https://doi.org/10.1016/j.surg.2021.05.055
https://doi.org/10.1016/j.surg.2021.05.055
Autor:
Theodora Pappa, Matthew A. Nehs, Iñigo Landa, Gerard M. Doherty, Erik K. Alexander, Hannah L. Johnson, Sara Ahmadi, Neal I. Lindeman, Jochen H. Lorch, Ellen Marqusee, Justine A. Barletta, Nancy L. Cho
Publikováno v:
Clinical Cancer Research. 27:4256-4264
Purpose: The extent to which routine genomic sequencing can identify relevant secondary genomic alterations among BRAFV600E-mutant papillary thyroid carcinoma (PTC) is unknown. Such markers would prove highly valuable for prognostic purposes. Experim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e2822ffc99ba7b77ae0bf5bf706e397
https://doi.org/10.1158/1078-0432.ccr-21-0874
https://doi.org/10.1158/1078-0432.ccr-21-0874