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Research 211–240 of 762
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- The Dermal Papilla: An Instructive Niche for Epithelial Stem and Progenitor Cells in Development and Regeneration of the Hair Follicle
- Feather arrays are patterned by interacting signalling and cell density waves
- Genetic prediction of male pattern baldness
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Biology and Genetics of Hair
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Inhibition of SARS-CoV-2 entry through the ACE2/TMPRSS2 pathway: a promising approach for uncovering early COVID-19 drug therapies
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Stem cell plasticity enables hair regeneration following Lgr5+ cell loss
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- What does acne genetics teach us about disease pathogenesis?
- Diagnostic approach to low‐renin hypertension
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia