Search
for
Sort by
Research 121–150 of 1000+
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- TLR2 Regulates Hair Follicle Cycle and Regeneration via BMP Signaling
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Ontogenetic Transition in Fetal Wound Transforming Growth Factor-β Regulation Correlates with Collagen Organization
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- Overexpression of Hedgehog Signaling Is Associated with Epidermal Tumor Formation in Vitamin D Receptor–Null Mice
- Transcutaneous electrical acustimulation promotes wound healing in mice by modulating signaling molecules and mitochondria function
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Regulation of stem cell function by protein ubiquitylation
- Plerixafor Biases CXCR4 Signaling Through β-Arrestin to Promote Melanogenesis via β-Catenin–MITF Activation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Atroposelective Synthesis of Biaryl <i>N</i>‐Oxides via Cu‐Catalyzed De Novo Heteroaromatic <i>N</i>‐Oxide Ring Formation
- Gene Expression Profiles of Melanocytes Over-Expressing miR-5110 in Alpaca
- Epidermal Notch signalling: differentiation, cancer and adhesion
- S100A6: molecular function and biomarker role
- The Vitamin D Receptor as Tumor Suppressor in Skin
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The Localization of Label-Retaining Cells in Mouse Nails
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- The potential of Clausena anisata (Willd.) Hook.f. ex Benth against Propionibacterium acnes