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Research 61–90 of 1000+
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Finding bald spots on chromosome 20p11
- Transcriptomic analysis of human skin wound healing and rejuvenation following ablative fractional laser treatment
- Structure of human type II 5 alpha-reductase gene.
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- Modelling androgen synthesis and action during human sexual differentiation
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- British Society for Dermatopathology
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Identification of key genes induced by platelet-rich plasma in human dermal papilla cells using bioinformatics methods
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- 5α-Reductase Inhibitors, Chemical and Clinical Models
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Effects of anticonvulsant drugs on chromosomes.
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis