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Research 541–570 of 565
- Ectodysplasin research—Where to next?
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co- option in the evolution of the hair follicle
- A Regulatory Loop between β-Catenin and Extra-cellular Matrix Components during the Proliferative Phase of Cutaneous Wound Healing
- Genetics of Alopecia
- Increased expression of Ectodysplasin A2 Receptor EDA2R is the most remarkable and ubiquitous aging-related transcriptional hallmark
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Mechanical properties characterization of human hair fibers cortex region by multiparametric Atomic Force Microscopy mapping
- Homeostatic maintenance of the murine corneal epithelium in pathophysiological contexts
- Mucocutaneous Findings and Endocrinopathies in Children with Turner Syndrome: A Cross-Sectional Study
- The Effect of the COVID-19 Pandemic on Stress-related Dermatologic Diseases.
- Dermatoloji ve Kozmetolojide D Vitamini
- Hypertrichosis around a leg ulcer being treated with prostaglandin E1 ointment
- Efficacy of topical 5% minoxidil versus oral 5mg biotin versus topical minoxidil and oral biotin on hair growth velocity in men: a randomized, crossover clinical trial
- Efeitos de diferentes doses do Minoxidil oral, em dois tempos de exposição, no complexo prostático de camundongos Balb/C
- Você conhece esta síndrome? * Do you know this syndrome? *
- Farmácia Queija Ferreira, Porto
- As manifestações dermatológicas da síndrome do ovário policístico: Uma revisão bibliográfica
- The efficiency of a complementary approach to Stein-Leventhal Syndrome (Polycystic Ovary Syndrome) - a comprehensive review
- Cyclodextrins as excipients in solid oral dosage forms
- Milk yield and hair coat characteristics of Holstein cows in a hot environment
- A alopecia no câncer de mama
- 0932 Spatiotemporal gradient of mesenchymal stiffness controls sweat gland morphogenesis
- What do we know about 5-alpha reductase inhibitors?
- Frontal fibrosing alopecia: a review of eleven patients
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Current Genetics in Hair Diseases
- Novel missense mutation in the EDA gene in a family affected by oligodontia