Preclinical Models of Rare Corneal and Ocular Surface Diseases: a Comprehensive Narrative Review. [PDF]
Lecchi EAL +7 more
europepmc +1 more source
Establishment of a Common Marmoset Lineage Carrying a Frameshift Mutation in SETD1A, a Schizophrenia Risk Gene. [PDF]
Wei Z +9 more
europepmc +1 more source
Aberrant phase separation from a rare ABI3 mutation drives microglial dysfunction and Alzheimer's risk. [PDF]
Li S +22 more
europepmc +1 more source
NF-κB across the Alzheimer disease spectrum: Context-dependent protective and pathogenic roles. [PDF]
Azargoonjahromi A +2 more
europepmc +1 more source
<i>In vitro</i> and <i>in vivo</i> studies on the impact of the familial adenomatous polyposis heterogeneous mutation MUC20-S671C on colorectal carcinogenesis and progression. [PDF]
Yan L +5 more
europepmc +1 more source
Functional divergence of Capicua isoforms explains differential tissue vulnerability in neurological disease. [PDF]
Lee H +11 more
europepmc +1 more source
Editorial: Technologies for RNA Detection. [PDF]
Savulescu AF +3 more
europepmc +1 more source
Common human ALDH1B1 and ALDH2 variants increase neuroinflammatory response to a single ethanol dose in mice. [PDF]
Seike T +4 more
europepmc +1 more source
Animal models for the study of ADHD: the need for next-generation models. [PDF]
Furuie H +5 more
europepmc +1 more source
Generation and Characterization of an Osteoclastic Cell Model of Gaucher's Bone Disease. [PDF]
Patiño-Salazar JD +14 more
europepmc +1 more source

