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Research 871–900 of 1000+
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Congenital triangular alopecia - A case report
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children
- Acquired Generalized Hypertrichosis Due to Diazoxide
- Alopecia and Periodontitis: Exploring the connecting dots
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Treatment of Alopecia in Children
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Gene Expression Analysis of Chondrogenic Markers in Hair Follicle Dermal Papillae Cells Under the Effect of Laser Photobiomodulation and the Synovial Fluid
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Dysfunction of keratinocyte adhesion
- Exploring the Differentiation Abilities of Hair Follicle and Dental Pulp Stem Cells Into Islet Like Cells
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Formulation and Evaluation of Herbal Hair Serum in Treatment of Various Hair- Related Problems
- THERAPEUTIC ASPECTS OF ONION IN TREATMENT OF CANCER AND RELATED ISSUES: A REVIEW
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Platelet Rich Plasma Treatment of Androgenetic Alopecia in Men and Women
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Mesenchymal stem cells and their extracellular vesicle-based therapies in skin and hair rejuvenation: a scoping review
- Fully functional hair follicle organ regeneration using organ-inductive potential stem cells with an accessory mesenchymal cell population in an in vitro culture system
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Morphological and Morphometric Analysis of Animal Hair From 18th Century Burial Sites in Mazamet (Southwest France)
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population