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Research 301–330 of 1000+
- 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
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- What does acne genetics teach us about disease pathogenesis?
- 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
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- 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
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- 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
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Genetic basis of polycystic ovary syndrome
- Analysis of lncRNAs Expression Profiles in Hair Follicle of Hu Sheep Lambskin
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- New small molecules in dermatology: for the autoimmunity, inflammation and beyond
- Physiology and Medical Treatments for Alopecia
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study