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Research 361–390 of 1000+
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Genetic Susceptibility to Alopecia
- Plant Extracts in Skin Care Products
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- CD4 expression controls epidermal stem cell balance
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Alopecia por diluição da cor em uma cadela Staffordshire Bull Terrier azul: Relato de caso
- Penis Endocrinology
- B‐ RAF , naevi and melanoma: a complex relationship
- Abstracts Pt.30
- Syndromes of Severe Insulin Resistance (SSIRs)
- Epidermal β-catenin activation remodels the dermis via paracrine signalling to distinct fibroblast lineages
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Behavioural characterization of Vitamin D receptor knockout mice
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation