Search
for
Sort by
Research 421–450 of 1000+
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- IL-15 in alopecia areata: the immune tolerance mechanistic insights and translational perspectives
- Systemic Lupus Erythematosus: What Every Clinician Needs to Know
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- CircERCC6 Positively Regulates the Induced Activation of SHF Stem Cells in Cashmere Goats via the miR-412-3p/BNC2 Axis in an m6A-Dependent Manner
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Alopecias
- SMC-specific IGF1 suppresses a 45 kDa LAMP2 isoform to mediate the anti-atherosclerotic effect of ferulic acid
- Coffea arabica: An Emerging Active Ingredient in Dermato-Cosmetic Applications
- International Society for the Study of Women's Sexual Health Clinical Practice Guideline for the Use of Systemic Testosterone for Hypoactive Sexual Desire Disorder in Women
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- A Rare Case of Cutis Verticis Gyrata with Underlying Cerebriform Intradermal Nevus
- A New Horizon in Facial Plastic Surgery: Skin Tissue-Engineering and Stem Cell Therapy—Reality or Dream?
- Possibilities and Limitations for Reversal of Age-Related Hair Loss
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Congenital adrenal hyperplasia
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- The human keratins: biology and pathology
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Gender differences in skin: A review of the literature
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Replicative stress, stem cells and aging
- Nonclassic adrenal hyperplasia
- Wnt signaling: the good and the bad
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- Alopecia Areata
- Main Plenary Sessions: Summaries of Papers
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia