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Research 781–810 of 1000+
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Confocal microscopy and optical coherence tomography of inflammatory skin diseases in hairs and pilosebaceous units: A systematic review
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Presence of mast cells and mast cell degranulation in scalp biopsies of telogen effluvium
- Monilethrix, a rare inherited hair shaft disorder in siblings
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Bioactive inorganic particles‐based biomaterials for skin tissue engineering
- Effect of discarded keratin-based biocomposite hydrogels on the wound healing process in vivo
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Serum biotin levels in women complaining of hair loss
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Causes and Management of Hypertrichosis
- Mechanical and Immunological Regulation in Wound Healing and Skin Reconstruction
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Psychological interventions in the management of common skin conditions
- Genetic Hair Disorders: A Review
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Transient agonism of the sonic hedgehog pathway triggers a permanent transition of skin appendage fate in the chicken embryo
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Porokeratotic eccrine ostial and dermal duct nevus: A noteworthy presentation
- Hair Follicle Morphogenesis During Embryogenesis, Neogenesis, and Organogenesis
- Monilethrix