Frontiers | Number of Candidate Effector Genes in Accessory Genomes Differentiates Pathogenic From Endophytic Fusarium oxysporum Strains
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Discovery of Sulanemadlin (ALRN-6924), the First Cell-Permeating, Stabilized α-Helical Peptide in Clinical Development | Journal of Medicinal Chemistry
Genetic basis of proteome variation in yeast | Nature Genetics
Allosteric activation of T cell antigen receptor signaling by quaternary structure relaxation - ScienceDirect
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Polyethylene Glycol Immunogenicity: Theoretical, Clinical, and Practical Aspects of Anti-Polyethylene Glycol Antibodies | ACS Nano
PPARγ (Peroxisome Proliferator-Activated Receptor γ) Deacetylation Suppresses Aging-Associated Atherosclerosis and Hypercholesterolemia | Arteriosclerosis, Thrombosis, and Vascular Biology
Inducible over‐expression of cardiac Nos1ap causes short QT syndrome in transgenic mice - Jänsch - 2023 - FEBS Open Bio - Wiley Online Library
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Time of day determines postexercise metabolism in mouse adipose tissue | PNAS
Co-condensation of proteins with single- and double-stranded DNA | PNAS
Protein-structure-guided discovery of functional mutations across 19 cancer types | Nature Genetics
Polyethylene Glycol Immunogenicity: Theoretical, Clinical, and Practical Aspects of Anti-Polyethylene Glycol Antibodies | ACS Nano
Polyethylene Glycol Immunogenicity: Theoretical, Clinical, and Practical Aspects of Anti-Polyethylene Glycol Antibodies | ACS Nano
Visible Light Induced Solubility Modulation of Polynorbornene Bearing Bridged 1,2‐Diketones - Kim - 2021 - Asian Journal of Organic Chemistry - Wiley Online Library
An allelic series of miR-17∼92–mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron | Nature Genetics
Human Neutrophil Peptide 1 Limits Hypercholesterolemia-induced Atherosclerosis by Increasing Hepatic LDL Clearance - eBioMedicine
Integrated genomic characterization of IDH1-mutant glioma malignant progression | Nature Genetics
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HIV integration in the human brain is linked to microglial activation and 3D genome remodeling - ScienceDirect
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture | Nature Genetics
