Search
for
Sort by
Research 271–300 of 391
- Enhancement of hair growth through stimulation of hair follicle stem cells by prostaglandin E2 collagen matrix
- Hair That Is Difficult to Manage in a Hispanic Girl
- New aspects of the structure of human hair on the basis of optical microscopic observations of disassembled hair parts.
- The Requirement to Monitor Low-dose Oral Minoxidil in the Management of Hair Loss
- Diffuse face and ear hypertrichosis caused by 5% topical minoxidil in an adult woman with spontaneous resolution
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Facial hair enhancement with minoxidil—an off-label use
- Hair Root Dermoscopy from Shed Hair: A Simple Diagnostic Tool in Telogen Effluvium
- Low-Dose Oral Minoxidil for Alopecia: A Comprehensive Review
- Oral minoxidil in trichology: A review
- Doctor, my armpit hair has turned yellow! Malodorous yellowish axillary hair in an adolescent patient
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- The Catalog of Human Hair Keratins
- Dermoscopy in General Dermatology: A Practical Overview
- Minoxidil and its use in hair disorders: a review
- Hox in hair growth and development
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Trichoscopy in alopecias: Diagnosis simplified
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Keratins and disease at a glance
- The molecular basis of human keratin disorders
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Trichoscopy (hair and scalp videodermoscopy) in the healthy female. Method standardization and norms for measurable parameters