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Research 511–540 of 1000+
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Human epithelial stem cell survival within their niche requires “tonic” cannabinoid receptor 1‐signalling—Lessons from the hair follicle
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- The hair shaft: normality, abnormality, and genetics
- Biotinidase deficiency characterized by skin and hair findings
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Epidermal expression of receptor for advanced glycation end products (RAGE) is related to inflammation and apoptosis in human skin
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Tetrahydroxystilbene Glucoside Effectively Prevents Apoptosis Induced Hair Loss
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- Woolly Antics between the Sheaths
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Severe Hypernatremia as Presentation of Netherton Syndrome
- COX2-ATP Synthase Regulates Spine Follicle Size in Hedgehogs
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese