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Research 121–150 of 1000+
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Clinical and epidemiological characteristics and associated factors of hair graying: a population-based, cross-sectional study in Turkey
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Retrospective Study about the Causes and the Effects of Korean Medicine Treatment on Alopecia - Focused on Acquired Febrile Alopecia -
- Isolation and Characterization of Cutaneous Epithelial Stem Cells
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Prevalence of Androgenetic Alopecia Among Adults in Sulaimani Governorate (2023): Epidemiology, Pathophysiology, and Clinical Implications
- Effects of different concentrations of androgens on KAP24.1 gene expression in Hetian sheep and Karakul sheep
- Viewpoint 1
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Editorial: Animal fibers
- Expression and Analysis of TBX3 Gene in the Skin from Three Locations on Dun Mongolian Bider Horse
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- A Powerful Method for Pleiotropic Analysis under Composite Null Hypothesis Identifies Novel Shared Loci Between Type 2 Diabetes and Prostate Cancer
- PARIETAL AND OCCIPITAL HAIR LOSS PATTERNS IN INITIAL STAGES OF ANDROGENIC ALOPECIA IN MEN
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease
- Finding bald spots on chromosome 20p11
- This Month in the Journal
- Whole-genome sequencing of eight goat populations for the detection of selection signatures underlying production and adaptive traits
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation