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Research 691–720 of 1000+
- Discovery and Functional Analysis of Secondary Hair Follicle miRNAs during Annual Cashmere Growth
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Human Hair and the Impact of Cosmetic Procedures: A Review on Cleansing and Shape-Modulating Cosmetics
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Screening of circRNAs Associated with Secondary Wool Follicle Development in Fine-Wool Sheep and Construction of Their ceRNA Network
- Formulation and Evaluation of Polyherbal Hair serum for Hair Strengthening and Antidandruff
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Parallels in signaling between development and regeneration in ectodermal organs
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- 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
- The fundamentals of WNT10A
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Early inductive events in ectodermal appendage morphogenesis
- Integumentary System
- Identification of a secreted BMP antagonist, ectodin, integrating BMP, FGF, and SHH signals from the tooth enamel knot
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Transcriptomic landscape of early hair follicle and epidermal development
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co- option in the evolution of the hair follicle
- Congenital atrichia associated with situs inversus and mesocardia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- N02. Hair and Nails
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ