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Research 811–840 of 1000+
- 1315 An Integrated model of alopecia areata biomarkers highlights both Th1/Th2 upregulation, with stronger correlations between Th2 activation and disease severity
- 1312 Nrf2 activation enhances the healing of cutaneous wounds through the activation of hair follicle stem cells
- 1311 Efficacy of topical tofacitinib in promoting hair growth in non-scarring alopecia
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Cycle pilaire et alopécie X chez le chien
- Australasian Society for Dermatology Research Meeting, May 2006
- Syndromes of Severe Insulin Resistance (SSIRs)
- Psychiatry, Medicine
- Dictionary
- Health Messages
- Skin precancer.
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Therapeutic effects of minoxidil high extra combination therapy in patients with androgenetic alopecia.
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Abstract 10845: Spontaneous Coronary Artery Dissection as the Primary Presentation of Ana-Negative Lupus
- [Treatment of androgenic alopecia with minoxidil].
- The investigation of insulin resistance and metabolic syndrome in male patients with early-onset androgenetic alopecia
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- A descriptive study of alopecia patterns and their relation to thyroid dysfunction
- Abstract ED05-04: Presurgical models to effectively screen preventive agents
- Adult bone-marrow-derived mesenchymal stem cells contribute to wound healing of skin appendages
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Pharmacologic Therapy of Polycystic Ovary Syndrome
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Congenital atrichia associated with nevus flammeus: A rare association
- Sex Hormones and Related Compounds, Including Hormonal Contraceptives
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Autosomal recessive hereditary hypotrichosis simplex: A case report