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Research 301–330 of 602
- Mnemonics in dermatology
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Metabolomic analysis of SMP30/GNL knockout mice treated with fermented vegetable and fruit extract (OM-X®)
- Female Antiandrogens
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Ingestion of topical steroid triggering pustular psoriasis?
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- A regenerative stem cell-derived matrix accelerates functional dermal wound repair in a preclinical diabetic model
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- An isotope dilution-liquid chromatography-tandem mass spectrometry-based candidate reference measurement procedure for the quantification of 5-alpha-dihydrotestosterone in human serum and plasma
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- LEADING SECTOR OF HEALTH TOURISM; HAIR TRANSPLANTATION APPLICATIONS: A BIBLIOMETRIC ANALYSIS
- Multidimensional assessment of adverse events of finasteride：a real-world pharmacovigilance analysis based on FDA Adverse Event Reporting System (FAERS) from 2004 to April 2024
- ラット精巣におけるビタミンD 代謝関連遺伝子の発現解析
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Integrating herbal components into pharmaceutical formulations for hair woes
- If Women Just had Their Hormones Back the Way they Were!
- Cosmetic Considerations in Dark-Skinned Patients
- En Coup de Sabre in a Pediatric Patient Treated With Calcipotriene
- Hair loss after covid 19 - case series
- Inherited Epidermolysis Bullosa: A Clinical Case
- Abstract presented at the Joint meeting of the 21st meeting of the Japanese Research Society of clinical anatomy and the 6th meeting of the Society for aging image
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- 877 Small T antigen from a folliculotropic polyomavirus activates canonical Wnt/β-catenin signaling in vivo
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation