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Research 181–210 of 1000+
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Polycystic ovarian syndrome: Prevalence and its correlates among adolescent girls
- Efficacy of Low-level Laser Therapy in Minimising Morbidity Associated with Removal of Impacted Mandibular Third Molar - A Comparative Study
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Steroids excreted by human skin. I. C19-steroids in axillary hair.
- Dental cell type atlas reveals stem and differentiated cell types in mouse and human teeth
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Developmental Plasticity of Patterned and Regenerating Oral Organs
- Mesenchymal stem cell‐derived exosomes for organ development and cell‐free therapy
- Molecular mechanisms of ectodermal dysplasia syndromes
- Stable Isotopes And Multiple Tissue Analysis: Reconstructing Life Histories For Individuals From Dakhleh Oasis, Egypt
- Pomegranate-peel-chitosan-gelatin composite: A hemostatic dental sponge with antibacterial enhancement
- PA05 A rare case of cardiocutaneous syndrome in a young child
- A girl struggling with extremely unruly hair
- Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Dermatologic Signs in Patients with Eating Disorders
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- 2,3,7,8‐Tetrachlorodibenzo‐<i>p</i>‐dioxin causes an increase in protein kinases growth hepatic associated with epidermal factor receptor in the plasma membrane
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Comparison of prevalence of periodontal disease in women with polycystic ovary syndrome and healthy controls
- Pharmacological Efficacy of Tamarix aphylla: A Comprehensive Review
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
- Thymosin β4 and Actin: Binding Modes, Biological Functions and Clinical Applications
- Light emitting diodes technology-based photobiomodulation therapy (PBMT) for dermatology and aesthetics: Recent applications, challenges, and perspectives
- Connexin mutations in human disease