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Research 91–120 of 1000+
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- 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
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Cicatricial alopecia
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- 601 Hair growth properties of Cinchona succirubra Extract, Leontopodium alpinum Extract and Manganese PCA in human hair follicle dermal papilla cells
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Anagen effluvium
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Biotin
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Discovery and Functional Analysis of Secondary Hair Follicle miRNAs during Annual Cashmere Growth
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Connexin mutations in human disease
- Diversity of Trichocyte Keratins and Keratin Associated Proteins