Thomas G. Boyer

ORCID: 0000-0002-9164-8712 · 7 papers in corpus
review 2026
Cells ·doi:10.3390/cells15090847

Chemical modifications of RNA add a dynamic regulatory layer to gene expression beyond the genome and epigenome. Among these modifications, 5-methylcytidine (m5C) has emerged as a key epitranscriptomic modification that influences RNA stabi…

review 2026
Biology ·doi:10.3390/biology15020142

Pseudouridine (Ψ), the most abundant RNA modification, plays essential roles in shaping RNA structure, stability, and translational output. Beyond cancer, Ψ is dynamically regulated across numerous physiological and pathological contexts-in…

review 2025
Cells ·doi:10.3390/cells14171380

Pseudouridylation, the most abundant RNA modification, plays a critical role in modulating RNA structure, stability, and function. Among the family of pseudouridine synthases, Pseudouridine Synthase 7 (PUS7) has recently gained attention fo…

lab-animal 2023
JCI insight ·doi:10.1172/jci.insight.171305

Uterine leiomyomas cause heavy menstrual bleeding, anemia, and pregnancy loss in millions of women worldwide. Driver mutations in the transcriptional mediator complex subunit 12 (MED12) gene in uterine myometrial cells initiate 70% of leiom…

review 2022
Endocrine Reviews ·doi:10.1210/endrev/bnab039

Uterine fibroids are benign monoclonal neoplasms of the myometrium, representing the most common tumors in women worldwide. To date, no long-term or noninvasive treatment option exists for hormone-dependent uterine fibroids, due to the limi…

lab-animal 2021
·doi:10.1096/fasebj.2021.35.s1.03798

Uterine fibroids are benign tumors that occur in the myometrium of the uterus. Although they are benign, they represent a significant health problem as they affect approximately 70% of women and cause pregnancy complications, infertility an…

other 2014
Cell reports ·doi:10.1016/j.celrep.2014.03.047

Somatic mutations in exon 2 of the RNA polymerase II transcriptional Mediator subunit MED12 occur at very high frequency (∼70%) in uterine leiomyomas. However, the influence of these mutations on Mediator function and the molecular basis fo…