Zobrazeno 1 - 10
of 307
pro vyhledávání: '"Neal I Lindeman"'
Autor:
Dai Fukumura, Rakesh K Jain, Peigen Huang, Lance L Munn, Patrik Andersson, Zohreh Amoozgar, Somin Lee, Meenal Datta, Sylvie Roberge, Mark Duquette, Neal I Lindeman, Shanmugarajan Krishnan, Sonu Subudhi, Ashwin Srinivasan Kumar, Jessica Posada, Pinji Lei
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss Suppl 2 (2023)
Externí odkaz:
https://doaj.org/article/3a4c2f3027794cf79400ff96ec785d88
Autor:
Sara M Tolaney, James Lindsay, Michael Manos, Biagio Ricciuti, Anita Giobbie-Hurder, Scott J Rodig, Joao V Alessi, Mark M Awad, Sandro Santagata, Bruce E Johnson, Glenn J Hanna, Elio Adib, Jason Weirather, Xinan Wang, Bijaya Sharma, Kathleen Pfaff, Kristen D Felt, William Lotter, Panagiotis Konstantinopoulos, Madison Turner, Federica Pecci, Emma L Welsh, Stephanie M Jones, Jennifer O Altreuter, Ian D Dryg, Alessandro Di Federico, Malini M Gandhi, Sabrina J Chan, Marta Holovatska, Melissa E Hughes, O’Meara Tess A, Neal I Lindeman, Jennifer Curtis, Peter K Sorger, Ethan Cerami, Lynette M Sholl, Jonathan A Novak
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/02ccda4c59ce49c1ba7f9100a145659a
Autor:
Diane R. Koeller, Danielle K. Manning, Alison Schwartz, Anu Chittenden, Connor P. Hayes, Feruza Abraamyan, Huma Q. Rana, Neal I. Lindeman, Judy E. Garber, Arezou A. Ghazani
Publikováno v:
MethodsX, Vol 9, Iss , Pp 101761- (2022)
The interpretation of hereditary genetic sequencing variants is often limited due to the absence of functional data and other key evidence to assess the role of variants in disease. Cancer genetics is unique, as two sets of genomic information are of
Externí odkaz:
https://doaj.org/article/87e8e139773c4bc2a908d6f6e6aedd90
Autor:
Danielle K. Manning, Priyanka Shivdasani, Diane R. Koeller, Alison Schwartz, Huma Q. Rana, Judy E. Garber, Neal I. Lindeman, Arezou A. Ghazani
Publikováno v:
Data in Brief, Vol 39, Iss , Pp 107653- (2021)
Von Hippel-Lindau (VHL) syndrome is a hereditary cancer genetic condition associated with inactivating pathogenic alterations in the VHL tumor suppressor gene located at 3p (short arm of chromosome 3). Classic features of VHL include clear cell renal
Externí odkaz:
https://doaj.org/article/2639378a2e4349219113d5d0a39e0357
Autor:
Roy S. Herbst, Dara L. Aisner, Joshua R. Sonett, Andrew T. Turk, Joshua L. Weintraub, Neal I. Lindeman
Publikováno v:
Frontiers in Medicine, Vol 7 (2021)
For patients with advanced non–small cell lung cancer, genomic profiling of tumors to identify potentially targetable alterations and thereby inform treatment selection is now part of standard care. While molecular analyses are primarily focused on
Externí odkaz:
https://doaj.org/article/812b166817254889a7a4f9f80084a0a8
Autor:
Jacob E. Berchuck, Daniel Boiarsky, Rebecca Silver, Rajitha Sunkara, Heather M. McClure, Harrison K. Tsai, Stephanie Siegmund, Alok K. Tewari, Jonathan A. Nowak, Neal I. Lindeman, Huma Q. Rana, Atish D. Choudhury, Mark M. Pomerantz, Matthew L. Freedman, Eliezer M. Van Allen, Mary-Ellen Taplin
Publikováno v:
JCO precision oncology. 6
PURPOSE Guidelines recommend somatic and germline testing for men with advanced prostate cancer (PCa). Barriers to widespread implementation result in underutilization of germline testing. Somatic testing alone risks missing pathogenic germline varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16d101d1034970b9e1b0a923de430c93
https://pubmed.ncbi.nlm.nih.gov/36103646
https://pubmed.ncbi.nlm.nih.gov/36103646
Autor:
Elizabeth Pan, Wanling Xie, Archana Ajmera, Arlene Araneta, Christina Jamieson, Edmund Folefac, Arif Hussain, Christos E. Kyriakopoulos, Adam Olson, Mamta Parikh, Rahul Parikh, Biren Saraiya, S. Percy Ivy, Eliezer M. Van Allen, Neal I. Lindeman, Bose S. Kochupurakkal, Geoffrey I. Shapiro, Rana R. McKay
Publikováno v:
Molecular Cancer Therapeutics. 22:511-518
Given that radium-223 is a radiopharmaceutical that induces DNA damage, and olaparib is a PARP inhibitor that interferes with DNA repair mechanisms, we hypothesized their synergy in metastatic castration-resistant prostate cancer (mCRPC). We sought t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd08ddb7e908aa341fa6a73a7134dded
https://doi.org/10.1158/1535-7163.mct-22-0583
https://doi.org/10.1158/1535-7163.mct-22-0583
Publikováno v:
Gynecologic Oncology Reports, Vol 28, Iss , Pp 15-17 (2019)
We report an extraordinary case of a woman, exposed to diethylstilbestrol in utero, who developed clear cell adenocarcinoma of the cervix with a concurrent polymerase-Ɛ (POLE) somatic mutation. The tumor exhibited the classic phenotypic characterist
Externí odkaz:
https://doaj.org/article/6622aea3749a4ed9a7e9dd2ccf44d0c2
Publikováno v:
The American Journal of Dermatopathology. 45:217-226
Proliferating pilar tumors (PPTs) are rare neoplasms of external root sheath derivation, which most commonly occur on the scalp of elderly women. Although typically showing classic histologic features such as trichilemmal type keratinization, a lobul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53ee264038c5d417c7212d074982c5e8
https://doi.org/10.1097/dad.0000000000002308
https://doi.org/10.1097/dad.0000000000002308
Publikováno v:
Cancer Epidemiol Biomarkers Prev
Background: In 2017, DNA mismatch repair/microsatellite instability (MMR/MSI) testing was nationally recommended for advanced colorectal cancers based on favorable immune checkpoint inhibitor responses among patients with MMR-deficient/MSI-high tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b976a3f9de282c4553eb66426da6ed56
https://doi.org/10.1158/1055-9965.epi-22-0279
https://doi.org/10.1158/1055-9965.epi-22-0279