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Research 271–300 of 1000+
- Role of Swasthavritta to maintain healthy hair
- Selected topics in pediatric hair loss
- Determination of Anti-Dandruff and Hair Growth Promoting Activity of combined coconut oil extract of Marking Nut
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Artepillin C and Other Herbal PAK1-blockers: Effects on Hair Cell Proliferation and Related PAK1-dependent Biological Function in Cell Culture
- Exosomes: A Promising Strategy for Repair, Regeneration and Treatment of Skin Disorders
- Kaempferol enhances hair growth by regulating JAK3/STAT6 and TGF-β/Smad signaling in human dermal papilla cells and a C57BL/6 mousemodel
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Adenosine Promotes Human Hair Growth and Inhibits Catagen Transition In Vitro: Role of the Outer Root Sheath Keratinocytes
- Neural Mechanisms of Hair Growth Control
- The role of marine-derived nutraceuticals in enhancing skin and hair health
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Autoimmune Disease Induction in a Healthy Human Organ: A Humanized Mouse Model of Alopecia Areata
- Skin features in myotonic dystrophy type 1: An observational study
- Alopecia areata: recognition, diagnosis and management
- Extensive Challenges and Pending Advances in the Study of 5-Alpha-Reductase Isoenzymes. A Literature Review
- Targeting receptor–regulator interactions
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Ptosis in childhood
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome