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Research 751–780 of 1000+
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- The spectrum of nephrocutaneous diseases and associations
- Infertility: Evaluation and Initial Management
- Darier Sign: A Historical Note
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Cronkhite-Canada Syndrome: A Case Report
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Clinical experience on follicular unit extraction megasession for severe androgenetic alopecia
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Microneedles as a perspective for transdermal therapeutic systems
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Hypothyroidism in Dogs
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- THE PEDIATRICIAN AND THE SEXUALLY ACTIVE ADOLESCENT
- The urine as a diagnostic key for a homozygous EGFR mutation
- Biotin
- Inconsolable Crying in Infants: Differential Diagnosis in the Pediatric Emergency Department
- The Relationship between Lichen Planus and Carotid Intima Media Thickness.
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Diagnosis and treatment of polycystic ovarian syndrome: an update
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Diuretics
- People’s experiences of eyebrow transplantation: A qualitative study