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Research 331–360 of 1000+
- Epidermal growth factor, innovation and safety
- Black dots in trichoscopy after COVID‐19. Can it be telogen effluvium?
- Molecular interactions of natural and synthetic steroids in female hamsters’ flank organs
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Stem cells and aberrant signaling of molecular systems in skin aging
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Genome-wide association study of skin complex diseases
- Efectos de la alteración de los niveles de allopregnanolona durante periodos críticos del neurodesarrollo en la vulnerabilidad al consumo de alcohol
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Laparoscopic Extirpation of Adrenal Gland Ganglioneuroma Incidentally Diagnosed during Evaluation for Patchy Alopecia Areata in an Adolescent Boy
- Androgen excess: a hallmark of polycystic ovary syndrome
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Management of CAH during pregnancy
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3
- Role of caffeine in the management of androgenetic alopecia
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Androgenic alopecia: A counterproductive outcome of the anabolic effect of androgens
- Full investigation of patients with polycystic ovary syndrome (PCOS) presenting to four different clinical specialties reveals significant differences and undiagnosed morbidity
- Neonatal allopregnanolone or finasteride administration modifies hippocampal K+ Cl− co-transporter expression during early development in male rats
- Relative binding affinity of novel steroids to androgen receptors in hamster prostate
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy