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Research 31–60 of 1000+
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- PCOS: update and diagnostic approach
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- Organization and Expression of Hair Follicle Genes.
- Alopecia totalis in an infant
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- A genetically informed brain atlas for enhancing brain imaging genomics
- Collective heterogeneity of mitochondrial potential in contact inhibition of proliferation
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
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- Outbreak of recombinant lumpy skin disease virus in yaks: high mortality and systemic pathogenesis in Qinghai-Tibet Plateau yak herds
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Research on Mental Stress Recognition of Depressive Disorders in Patients With Androgenic Alopecia Based on Machine Learning and Fuzzy K-Means Clustering
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Hair cluster detection model based on dermoscopic images
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- What does acne genetics teach us about disease pathogenesis?
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Polarized microscopy in genetic hair disorders: case series
- Recent advances in the genetics of alopecia areata
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria