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Research 601–630 of 1000+
- Significance of stress keratin expression in normal and diseased epithelia
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Transcutaneous electrical acustimulation promotes wound healing in mice by modulating signaling molecules and mitochondria function
- Exploring the Role of GLP‐1 Agents in Managing Diabetic Foot Ulcers: A Narrative and Systematic Review
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Skin regeneration with conical and hair follicle structure of deep second-degree scalding injuries via combined expression of the EPO receptor and beta common receptor by local subcutaneous injection of nanosized rhEPO
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- CME examination
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Cell Cycle Regulation and Regeneration
- Formulation and Evaluation of PLGA Nanoparticulate-Based Microneedle System for Potential Treatment of Neurological Diseases
- A Screening Study on Dermatoses in Pregnancy
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Hair care practices and scalp/hair disease in African American girls
- 282 WITHDRAWN
- Efluvio anágeno. Hallazgos tricoscópicos
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Multicolor Cell Barcoding Technology for Long-Term Surveillance of Epithelial Regeneration in Zebrafish
- Loose anagen hair of childhood: The phenomenon of easily pluckable hair
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Anticancer effects of metformin on neuroendocrine tumor cells in vitro
- Contraception and the dermatologist
- <i>In Vitro</i> Analysis of Finasteride Activity against Candida albicans Urinary Biofilm Formation and Filamentation
- Sequence and expression of human hair keratin genes
- Forehead reduction and orbital contouring in facial feminisation surgery for transgender females