Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lisa Teot"'
Autor:
Lin Xu, Joshua L. Pierce, Angelica Sanchez, Kenneth S. Chen, Abhay A. Shukla, Nicholas J. Fustino, Sarai H. Stuart, Aditya Bagrodia, Xue Xiao, Lei Guo, Mark D. Krailo, Furqan Shaikh, Deborah F. Billmire, Farzana Pashankar, Jessica Bestrashniy, J. Wolter Oosterhuis, Ad J. M. Gillis, Yang Xie, Lisa Teot, Jaume Mora, Jenny N. Poynter, Dinesh Rakheja, Leendert H. J. Looijenga, Bruce W. Draper, A. Lindsay Frazier, James F. Amatruda
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Abstract Germ cell tumors (GCTs) are neoplasms of the testis, ovary and extragonadal sites that occur in infants, children, adolescents and adults. Post-pubertal (type II) malignant GCTs may present as seminoma, non-seminoma or mixed histologies. In
Externí odkaz:
https://doaj.org/article/7de0ec00eddb4344af90c7a9512816da
Autor:
Steven G. DuBois, Mark D. Krailo, Julia Glade-Bender, Allen Buxton, Nadia Laack, R. Lor Randall, Helen X. Chen, Nita L. Seibel, Matthew Boron, Stephanie Terezakis, Christine Hill-Kayser, Andrea Hayes, Joel M. Reid, Lisa Teot, Dinesh Rakheja, Richard Womer, Carola Arndt, Stephen L. Lessnick, Brian D. Crompton, E. Anders Kolb, Heike Daldrup-Link, Eric Eutsler, Damon R. Reed, Katherine A. Janeway, Richard G. Gorlick
Publikováno v:
Journal of Clinical Oncology. 41:2098-2107
PURPOSE Monoclonal antibodies directed against insulin-like growth factor-1 receptor (IGF-1R) have shown activity in patients with relapsed Ewing sarcoma. The primary objective of Children's Oncology Group trial AEWS1221 was to determine if the addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::161510daef43486d7607a1274091fcff
https://doi.org/10.1200/jco.22.01815
https://doi.org/10.1200/jco.22.01815
Autor:
Douglas Fair, Luke Maese, Yueh‐Yun Chi, Minjie Li, Douglas S. Hawkins, Rajkumar Venkatramani, Erin Rudzinski, David Parham, Lisa Teot, David Malkin, Sharon E. Plon, He Li, Aniko Sabo, Philip J. Lupo, Joshua D. Schiffman
Rhabdomyosarcoma (RMS) is a well-described cancer in Li-Fraumeni Syndrome (LFS), resulting from germline TP53 pathogenic variants (PVs). RMS exhibiting anaplasia (anRMS) have been associated with a high rate of germline TP53 PVs. This study provides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63f172c6ab3570b539cd45717c6816fe
https://doi.org/10.22541/au.165009784.45190592/v1
https://doi.org/10.22541/au.165009784.45190592/v1
Autor:
Jennifer R, Charlton, Weizhen, Tan, Ghaleb, Daouk, Lisa, Teot, Seymour, Rosen, Kevin M, Bennett, Aleksandra, Cwiek, Sejin, Nam, Francesco, Emma, François, Jouret, João Paulo, Oliveira, Lisbeth, Tranebjærg, Carina, Frykholm, Shrikant, Mane, Friedhelm, Hildebrandt, Tarak, Srivastava, Tina, Storm, Erik Ilsø, Christensen, Rikke, Nielsen
Publikováno v:
Am J Physiol Renal Physiol
Pathogenic variants in the LRP2 gene, encoding the multiligand receptor megalin, cause a rare autosomal recessive syndrome: Donnai-Barrow/Facio-Oculo-Acoustico-Renal (DB/FOAR) syndrome. Because of the rarity of the syndrome, the long-term consequence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6284f1b2795e25704f8e5de322b344ff
https://pubmed.ncbi.nlm.nih.gov/33103447
https://pubmed.ncbi.nlm.nih.gov/33103447
Autor:
Joan L. Leeson, Thom E. Lobe, Eugene S. Wiener, Timothy J. Triche, Philip P. Breitfeld, Richard J. Andrassy, Douglas S. Hawkins, Sarah S. Donaldson, R. Beverly Raney, Michael P. Link, Moody D. Wharam, William H. Meyer, W. Archie Bleyer, Carola A.S. Arndt, Frederick B. Ruymann, Lisa Teot, John C. Breneman, Eric Sandler, David M. Parham, Lisa A. Teot, Sharon E. Murphy, William M. Crist, Teresa J. Vietti, Frederic G. Barr, K. Scott Baker, David O. Walterhouse, Lynn M. Smith, Leslie L. Robison, Suzanne L. Wolden, Alberto S. Pappo, Jeff M. Michalski, Peter J. Houghton, Julia A. Bridge, James R. Anderson, Charles N. Paidas, Stephen J. Qualman, Harold M. Maurer, Holcombe E. Grier, Elizabeth Lyden, Ken M. Brown, Richard B. Womer, Poul H. Sorensen
Publikováno v:
Journal of Pediatric Hematology/Oncology. 23:225-233
Purpose: This study was designed to estimate the partial and complete response rates (CR and PR) of two novel drug pairs (vincristine and melphalan vs. ifosfamide and etoposide) and to improve overall survival of previously untreated patients with me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d88c09b6a9ee6017550bcf7d4b20dab
https://doi.org/10.1097/00043426-200105000-00010
https://doi.org/10.1097/00043426-200105000-00010
Autor:
Beverly, Raney, Winston, Huh, Douglas, Hawkins, Andrea, Hayes-Jordan, Lynn, Million, David, Rodeberg, Lisa, Teot, James, Anderson
Publikováno v:
Pediatric bloodcancer. 60(3)
We wanted to ascertain patterns of recurrence, re-treatment, and outcome among 188 eligible patients treated for localized orbital sarcoma on IRSG Protocols III/IV, 1984-1997.Retrospective chart review.Twenty-four of 188 patients (12.8%) developed lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06afa6e40fb8e35cf2f18687fecc07f3
https://pubmed.ncbi.nlm.nih.gov/22961750
https://pubmed.ncbi.nlm.nih.gov/22961750