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Blood Advances|June 17, 2026
Functional analysis of germline RUNX1 variants identified in individuals with suspected familial platelet disorderAna Catarina Menezes, Natalie T Deuitch, Aidan Pintuff, et al.
Frontiers in Immunology|September 10, 2021
The Cancer Epitope Database and Analysis Resource: A Blueprint for the Establishment of a New Bioinformatics Resource for Use by the Cancer Immunology CommunityZeynep Koşaloğlu-Yalçın, Nina Blazeska, Hannah Carter, et al.
Plos Genetics|January 30, 2013
A hybrid likelihood model for sequence-based disease association studiesYun-Ching Chen, Hannah Carter, Jennifer Parla, et al.
Science Advances|September 20, 2024
Prediction of immunotherapy response using mutations to cancer protein assembliesJungHo Kong, Xiaoyu Zhao, Akshat Singhal, et al.
Genome Medicine|September 10, 2021
Non-cancer-related pathogenic germline variants and expression consequences in ten-thousand cancer genomesZishan Wang, Xiao Fan, Yufeng Shen, et al.
Journal of Immunotherapy and Precision Oncology|August 28, 2023
Autoimmune HLA Alleles and Neoepitope Presentation Predict Post-Allogenic Transplant RelapseAndrea Castro, Aaron M Goodman, Zachary Rane, et al.
Cell Reports|July 5, 2024
Interface-guided phenotyping of coding variants in the transcription factor RUNX1Kivilcim Ozturk, Rebecca Panwala, Jeanna Sheen, et al.
Journal of Medical Imaging and Radiation Oncology|October 7, 2015
Testing the Assessment of New Radiation Oncology Technology and Treatments framework using the evaluation of post-prostatectomy radiotherapy techniquesGillian M Duchesne, Annette Haworth, Eric Bone, et al.
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