High-throughput evaluation of in vitro CRISPR activities enables optimized large-scale multiplex enrichment of rare variants
High-throughput evaluation of in vitro CRISPR activities enables optimized large-scale multiplex enrichment of rare variants
Comprehensive resistance profiling of chronic myeloid leukaemia associated ABL1 variants against five tyrosine kinase inhibitors using prime editing
Comprehensive resistance profiling of chronic myeloid leukaemia associated ABL1 variants against five tyrosine kinase inhibitors using prime editing
Gene supplementation with precise transgene expression rescues hearing loss in a mouse model with an Mpzl2 East Asian founder variant
Gene supplementation with precise transgene expression rescues hearing loss in a mouse model with an Mpzl2 East Asian founder variant
Identification of potential therapeutic targets for problematic alcohol use using multi-omics data
Identification of potential therapeutic targets for problematic alcohol use using multi-omics data
EBioMedicine, DOI: 10.1016/j.ebiom.2025.105939
2025-10
의약학
한빛사논문
강문일/upload/board/files/hbs_author/author_2/0043832_1.png(Boston University School of Medicine (현 숙명여자대학교 약학대학))강문일
Novel Genetic Loci for Nontuberculous Mycobacterial Pulmonary Disease and Potential Protective Effect of Body Mass Index
Novel Genetic Loci for Nontuberculous Mycobacterial Pulmonary Disease and Potential Protective Effect of Body Mass Index
Am. J. Respir. Crit. Care Med., DOI: 10.1164/rccm.202406-1253OC
[CORRESPONDENCE] Clinical Validation of Optical Genome Mapping in Multiple Myeloma Without Plasma Cell Enrichment
[CORRESPONDENCE] Clinical Validation of Optical Genome Mapping in Multiple Myeloma Without Plasma Cell Enrichment
Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2
Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2
MUTE-Seq: An Ultrasensitive Method for Detecting Low-Frequency Mutations in cfDNA With Engineered Advanced-Fidelity FnCas9
MUTE-Seq: An Ultrasensitive Method for Detecting Low-Frequency Mutations in cfDNA With Engineered Advanced-Fidelity FnCas9