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Nucleic Acids Research|September 25, 1991
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII geneE G Tuddenham, D N Cooper, J Gitschier, et al.
Human Mutation|March 7, 2014
Elucidating common structural features of human pathogenic variations using large-scale atomic-resolution protein networksJishnu Das, Hao Ran Lee, Adithya Sagar, et al.
British Journal of Cancer|October 1, 2008
Cancer survival in England and Wales at the end of the 20th centuryB Rachet, L M Woods, E Mitry, et al.
Cancer Gene Therapy|May 15, 2018
Regulated intratumoral expression of IL-12 using a RheoSwitch Therapeutic System® (RTS®) gene switch as gene therapy for the treatment of gliomaJohn A Barrett, Hongliang Cai, John Miao, et al.
American Journal of Human Genetics|March 25, 2026
Genome-wide detection of human 5' UTR variants that impact protein translationMatthieu Chaldebas, Khoren Ponsin, Jonathan Bohlen, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 1, 1997
Phase I study of 3'-deamino-3'-(2-methoxy-4-morpholinyl)doxorubicin (FCE 23762, PNU 152243) administered on a daily x3 scheduleM J Ratain, L A Skoog, S M O'Brien, et al.
Frontiers in Genetics|August 23, 2021
Splicing Outcomes of 5' Splice Site GT>GC Variants That Generate Wild-Type Transcripts Differ Significantly Between Full-Length and Minigene Splicing AssaysJin-Huan Lin, Hao Wu, Wen-Bin Zou, et al.
Human Gene Therapy|April 12, 2018
Preclinical Efficacy and Safety of CD19CAR Cytokine-Induced Killer Cells Transfected with Sleeping Beauty Transposon for the Treatment of Acute Lymphoblastic LeukemiaChiara F Magnani, Claudia Mezzanotte, Claudia Cappuzzello, et al.
Journal of Clinical Medicine|June 13, 2025
Decoding SCN2A Variants: Bridging Genetics and Phenotypes in Autism Spectrum DisorderNicholas DiStefano, Jaimee N Cooper, David H Elisha, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2026
Predicting interaction-specific protein-protein interaction perturbations by missense variants with MutPred-PPIRoss Stewart, Florent Laval, Georges Coppin, et al.
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