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Research 91–120 of 1000+
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- Characterisation of Four New Genes in the Ovine KAP19 Family
- BJD Editor's Choice
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Past, Present and Future Perspectives of Forensic Genetics
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Disease causing homozygous variants in the human hairless gene
- Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Genome-wide association study of skin complex diseases
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice