Associated Papers
Loss of EB2 delays mitotic progression in murine and human neural progenitors.
Phillips AW et al.
Development (cambridge, England), 2026
CircAGFG1 acts as a sponge of miR-4306 to stimulate esophageal cancer progression by modulating MAPRE2 expression.
Zhang D et al.
Acta Histochemica, 2021
MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome.
Thues C et al.
Scientific Reports, 2021
A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2.
Feng J et al.
Molecular Genetics & Genomic Medicine, 2020
Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.
Dentici ML et al.
Clinical Genetics, 2018
Zebrafish models of orofacial clefts.
Duncan KM et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2017
Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.
Isrie M et al.
American Journal of Human Genetics, 2015
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