Brian T. Wilson
Newcastle Upon Tyne, ENG NE13BZ, United Kingdom
Last Updated: 09/26/2026
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Found 21 publications
A New GlyT2 Variant Associated with Hyperekplexia.
Journal: International journal of molecular sciences
Published: May 16, 2025
Non-Immune Hydrops Fetalis, Multifocal Chorangiomatosis, and Noonan Syndrome 8.
Journal: Congenital anomalies
Published: December 24, 2024
ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients.
Journal: The Journal of experimental medicine
Published: April 03, 2020
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2.
Journal: American journal of human genetics
Published: February 15, 2020
Joining the hidden revolution in rare diseases: working with family support groups.
Journal: Archives of disease in childhood
Published: March 13, 2019
Functional characterisation of a novel ovarian cancer cell line, NUOC-1.
Journal: Oncotarget
Published: July 28, 2016
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.
Journal: Nature genetics
Published: April 19, 2016
Glycosylation is an Androgen-Regulated Process Essential for Prostate Cancer Cell Viability.
Journal: EBioMedicine
Published: February 25, 2016
Uterine carcinosarcoma/malignant mixed Müllerian tumor incidence is increased in women with breast cancer, but independent of hormone therapy.
Journal: Journal of gynecologic oncology
Published: September 02, 2015
The androgen receptor controls expression of the cancer-associated sTn antigen and cell adhesion through induction of ST6GalNAc1 in prostate cancer.
Journal: Oncotarget
Published: September 02, 2015
Metronidazole Toxicity in Cockayne Syndrome: A Case Series.
Journal: Pediatrics
Published: August 26, 2015
Last Updated: 09/26/2026