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Research 571–600 of 1000+
- CLINICAL PROFILE AND OUTCOMES OF PATIENTS WITH POLYCYSTIC OVARIAN SYNDROME
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Exploring climate adaptation in European Merino sheep: a landscape genomics approach
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Understanding the Secular Decline in Testosterone: Mechanisms, Consequences, and Clinical Perspectives
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Long-lived proteins and DNA as candidate predictive biomarkers for tissue associated diseases
- Construction of a cDNA library and identification of genes from Liaoning cashmere goat
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Dermatologic care of patients with differences of sex development
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- Propecia-induced spermatogenic failure: a report of two cases
- 85 Primary cutaneous follicle center lymphoma spans yet unrecognised subtypes including polyclonal reactions
- Hair follicle-specific keratins and their diseases
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research