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Introns

Prenatal stress increases corticosterone levels in offspring by impairing placental glucocorticoid barrier function

Can Liu, Hongya Liu, [ ... ], Suzhen Guan

Whole genome DNA methylation patterns in tissue and cfDNA associated with fibrosis reflect the complex signature of MASLD

Jongseong Ahn, Soyeon Kim, [ ... ], Jung Weon Lee

Association analysis of PAEP, KRT10, and BMP7 genes SNPs with reproductive traits in Kele pigs

Yong Zhao, Chunyuan Wang, [ ... ], Yiyu Zhang

LINE-1 transposition into murine Thyroglobulin results in congenital thyroid dysplasia

Wendy J. Bailey, Bart M. G. Smits, [ ... ], Thomas Forest

Genetic variability in ADAM17/TACE is associated with sporadic Alzheimer’s disease risk, neuropsychiatric symptoms and cognitive performance on the Rey Auditory Verbal Learning and Clock Drawing Tests

Francesco Bruno, Mirella A. Aceto, [ ... ], Alberto Montesanto

Mapping the temporal transcriptomic signature of a viral pathogen through CAGE and nanopore sequencing

Dóra Tombácz, Balázs Kakuk, [ ... ], Zsolt Boldogkői

Fibroblast growth factor receptor 2 (FGFR2) genetic polymorphisms contribute to fused roots in human molars

Sandra Regina Santos Meyfarth, Flares Baratto-Filho, [ ... ], Erika Calvano Küchler

The Arabidopsis thaliana core splicing factor PORCUPINE/SmE1 requires intron-mediated expression

Varvara Dikaya, Nelson Rojas-Murcia, [ ... ], Markus Schmid

Genomic analysis of bovine respiratory disease resistance in preweaned dairy calves diagnosed by a combination of clinical signs and thoracic ultrasonography

Maria G. Strillacci, Vincenzo Ferrulli, [ ... ], Antonio Boccardo

Trypanosomes lack a canonical EJC but possess an UPF1 dependent NMD-like pathway

Bernardo Papini Gabiatti, Eden Ribeiro Freire, [ ... ], Martin Zoltner

Mis-splicing drives loss of function of p53^E224D point mutation

Ian C. Lock, Nathan H. Leisenring, [ ... ], David G. Kirsch

Enrichment of rare CFTR variants in Finnish patients with congenital chloride diarrhea

Satu Wedenoja, Jarmo Ritari, [ ... ], Kaija-Leena Kolho

PCK1 and SLC22A2 gene variants associated with response to metformin treatment in type 2 diabetes

Sophie St-Amour, Laurence Tessier, [ ... ], Karine Tremblay

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