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Research 121–150 of 1000+
- Molecular genetics of androgen insensitivity
- Biomaterial-based mechanical regulation facilitates scarless wound healing with functional skin appendage regeneration
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Viable vs. Nonviable Microbiota Evaluation of the Hair Follicle and Scalp Microbiome
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Issue Information - TOC
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Regulation of self-renewal in colorectal cancer cell models
- Epigenetics of Colorectal Cancer
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Inflammatory auxo-action in the stem cell division theory of cancer
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- The Role of Histone Demethylases in Disease
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart