Salivary gland function, development, and regeneration

AM Chibly, MH Aure, VN Patel… - Physiological …, 2022 - journals.physiology.org
Salivary glands produce and secrete saliva, which is essential for maintaining oral health
and overall health. Understanding both the unique structure and physiological function of …

[HTML][HTML] Neurocristopathies: New insights 150 years after the neural crest discovery

GA Vega-Lopez, S Cerrizuela, C Tribulo… - Developmental biology, 2018 - Elsevier
The neural crest (NC) is a transient, multipotent and migratory cell population that generates
an astonishingly diverse array of cell types during vertebrate development. These cells …

[图书][B] Oral pathology: clinical pathologic correlations

JA Regezi, J Sciubba, RCK Jordan - 2016 - books.google.com
Diagnose oral diseases quickly and accurately! Oral Pathology: Clinical Pathologic
Correlations, 7th Edition presents diseases and conditions by appearance and presentation …

A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation

K Adhikari, M Fuentes-Guajardo… - Nature …, 2016 - nature.com
We report a genome-wide association scan for facial features in∼ 6,000 Latin Americans.
We evaluated 14 traits on an ordinal scale and found significant association (P values< 5× …

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway

JT Wright, M Fete, H Schneider, M Zinser… - American Journal of …, 2019 - Wiley Online Library
An international advisory group met at the National Institutes of Health in Bethesda,
Maryland in 2017, to discuss a new classification system for the ectodermal dysplasias …

Modeling recent human evolution in mice by expression of a selected EDAR variant

YG Kamberov, S Wang, J Tan, P Gerbault, A Wark… - Cell, 2013 - cell.com
An adaptive variant of the human Ectodysplasin receptor, EDARV370A, is one of the
strongest candidates of recent positive selection from genome-wide scans. We have …

Mutations in WNT10A are present in more than half of isolated hypodontia cases

MJ van den Boogaard, M Créton… - Journal of medical …, 2012 - jmg.bmj.com
Background Dental agenesis is the most common, often heritable, developmental anomaly
in humans. Mutations in MSX1, PAX9, AXIN2 and the ectodermal dysplasia genes EDA …

Sweat gland progenitors in development, homeostasis, and wound repair

C Lu, E Fuchs - Cold Spring Harbor perspectives …, 2014 - perspectivesinmedicine.cshlp.org
The human body is covered with several million sweat glands. These tiny coiled tubular skin
appendages produce the sweat that is our primary source of cooling and hydration of the …

Spatiotemporal antagonism in mesenchymal-epithelial signaling in sweat versus hair fate decision

CP Lu, L Polak, BE Keyes, E Fuchs - Science, 2016 - science.org
INTRODUCTION Across the vertebrate kingdom, epithelial appendages—including
mammary, sweat, and salivary glands; hair follicles (HFs); teeth; scales; and feathers—begin …

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation

M Xu, J Horrell, M Snitow, J Cui, H Gochnauer… - Nature …, 2017 - nature.com
Human WNT10A mutations are associated with developmental tooth abnormalities and
adolescent onset of a broad range of ectodermal defects. Here we show that β-catenin …