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Research 481–510 of 1000+
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- The genetic basis of dermatophytosis skin infection susceptibility
- Genetic Fate Mapping Using Site-Specific Recombinases
- Molecular Genetics of Alopecias
- Genetic Susceptibility to Alopecia
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Polarized microscopy in genetic hair disorders: case series
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Re: Associations Between Variants in the Cyclooxygenase 2 Enzyme Gene (PTGS2) and Development of Benign Prostate Enlargement
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Biology and Genetics of Hair
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
- Dermatopathology and molecular genetics
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- The hair shaft: normality, abnormality, and genetics
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Melanotrichoblastoma: A Histopathological Case Report of a Rare Pigmented Variant of Trichoblastoma