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Research 391–420 of 1000+
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Clonal expansion from standing genetic variation underpins the evolution of an emerging plant pathogen in Australia
- Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Impact of Premature Greying of Hair on Socio-cultural Adjustment and Self-esteem among Medical Undergraduates in Foundation University, Islamabad
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Why Some Women Look Young for Their Age
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- PEDL-XAI: A Hybrid Probabilistic Ensemble Deep Learning Approach for Hair Disorder Diagnosis
- On the etiology of vitiligo and gray hair
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Aging, alopecia, and stem cells
- Genetic Defects of Female Sexual Differentiation
- Polarized microscopy in genetic hair disorders: case series
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Genetic prediction of male pattern baldness
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders