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Research 181–210 of 1000+
- Do we need hair follicle stem cells and hair follicle neogenesis to cure common hair loss disorders?
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Alopecia in a 19-Month-Old Boy
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Anatomy and Biology of Hair at Different Ages
- Canine Follicle Stem Cell Candidates Reside in the Bulge and Share Characteristic Features with Human Bulge Cells
- [Hyperandrogenism and pilosebaceous follicles].
- Learning from nudity: lessons from the nude phenotype
- Comparative efficacy of oral dutasteride and low-, medium-, and high-dose oral minoxidil: a six-month prospective trichoscopic and clinical study
- Dermoscopy: what's new?
- Lichen Planopilaris in the Androgenetic Alopecia Area: A Pitfall for Hair Transplantation
- Comma Hairs: A New Dermoscopic Marker for Tinea Capitis
- Hair follicle organoids: advances in construction, applications, and translational challenges
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Artificial Intelligence as the New Backbone of Aesthetic Practice in India: A Comprehensive, Fully Referenced Industry Whitepaper
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Nutrition and Hair
- A Multidimensional Text Mining Approach to Analyze Research Trends on Scalp and Hair in Korea
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A case of congenital pili multigemini
- Pili annulati with fragility: Electron microscopic findings of a case
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis