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Research 181–210 of 1000+
- Bicalutamide 25 mg associated with minoxidil 1 mg versus minoxidil 1 mg for female-pattern hair loss: A randomized double-blind clinical trial
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Current Genetics in Hair Diseases
- Congenital hair loss disorders: Rare, but not too rare
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Morpho-Regulation of Ectodermal Organs
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Laser-Induced Koebner-Related Skin Reactions: A Clinical Overview
- Does a male polycystic ovarian syndrome equivalent exist?
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- A randomized double-blind placebo-controlled pilot study to assess the efficacy of a 24-week topical treatment by latanoprost 0.1% on hair growth and pigmentation in healthy volunteers with androgenetic alopecia
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Female pattern hair loss
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- <i>WNT10A</i> , dermatology and dentistry
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Topical minoxidil effectiveness in enhancing facial aesthetics: A systematic review and meta-analysis
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament