Search
for
Sort by
Research 511–540 of 1000+
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Genetic and molecular aspects of androgenetic alopecia
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Cell death by cornification
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- The molecular basis of human keratin disorders
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Genetic Hair Disorders: A Review
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Epidemiologic Study of Gene Distribution in Romanian and Brazilian Patients with Non-Cicatricial Alopecia
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens