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Research 601–630 of 1000+
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Report from the Cicatricial Alopecia Colloquium
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Assessing the role of stressful life events in the induction and recurrence of alopecia areata: A case-control study
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Prevalence and treatment of Alopecia areata in Taif area, KSA
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Exploration of Potential Secondary Plant Metabolites for the Treatment of Alopecia Areata
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Epidemiological Analysis of Alopecia in Migrant Communities at Dr. Hair™ Clinics
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability