Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bei Hopkins"'
Autor:
Kristin Roman, Bethany Remeniuk, Qingyan Au, Erinn Parnell, Sara Pollan, Arezoo Hanifi, Bei Hopkins, Natalie Monteiro, Harry Nunns, Josette William
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
Externí odkaz:
https://doaj.org/article/719bbc4a74ca4d3ebbc6d484b2f13ce5
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
Externí odkaz:
https://doaj.org/article/a11119f6b1824bedbaed14e89c5bbc3d
Publikováno v:
Regular and Young Investigator Award Abstracts.
Autor:
Nicole Couper, Bethany Remeniuk, Karen McClymont, Bei Hopkins, Natalie Monteiro, Lorcan Sherry, Darren Locke
Publikováno v:
Regular and Young Investigator Award Abstracts.
Autor:
Lorcan Sherry, Nicole Couper, Bethany Remeniuk, Karen McClymont, Bei Hopkins, Natalie Monteiro, Gabriel Reines March, Darren Locke
Publikováno v:
Cancer Research. 83:4633-4633
Non-small cell lung cancer (NSCLC) is a complex disease with varying pathological subtypes including adenocarcinomas and squamous cell carcinomas. After diagnosis, tumor staging provides important information about the extent of cancer in the body an
Autor:
Bei Hopkins, Steven J. Samuelsson, Terence Ta, Haiyan Jiang, Dawn Ciulla, Morgan L. Maeder, Joy E. Horng, Ari E. Friedland, Hoson Chao, Timothy Fennell, Georgia Giannoukos, Maxwell N. Skor, Sebastian Gloskowski, Christine D. Wilson, Rina Mepani, Diana Tabbaa, Gregory Gotta, Vic E. Myer, Jennifer A. DaSilva, Reshica Baral, Eugenio Marco, Alexandra Glucksmann, Deepak Reyon, Vidya Dhanapal, David Bumcrot, Luis A. Barrera, Shivangi Joshi, Tongyao Wang, Michael Stefanidakis, Abhishek Dass, Charles F Albright, Clifford Yudkoff, George S. Bounoutas, Scott Haskett, Shen Shen, Pam Stetkiewicz, Hariharan Jayaram
Publikováno v:
Nature Medicine. 25:229-233
Leber congenital amaurosis type 10 is a severe retinal dystrophy caused by mutations in the CEP290 gene1,2. We developed EDIT-101, a candidate genome-editing therapeutic, to remove the aberrant splice donor created by the IVS26 mutation in the CEP290
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
BackgroundMedulloblastoma recurrence occurs in approximately 30% of patients and is universally fatal, presenting one of the most significant unmet clinical challenges in pediatric oncology. It is now clear that medulloblastomas are complex ecosystem
Autor:
Tracey Blanchet, Manas K. Majumdar, Nancy Stedman, Elisabeth A. Morris, Bei Hopkins, S.S. Glasson, Scott H. Schelling, Roger Askew
Publikováno v:
Arthritis & Rheumatism. 56:3670-3674
Objective To phenotypically characterize ADAMTS-4– and ADAMTS-5–double-knockout mice, and to determine the effect of deletion of ADAMTS-4 and ADAMTS-5 on the progression of osteoarthritis (OA) in mice. Methods Mice lacking the catalytic domain of