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Research 481–510 of 802
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Hair Growth Defects of Diabetic and Hypercholesterolemic Wistar Albino Rats and Amelioration of Fish Oil-Treatment
- Registrars’ Symposium: Summaries of Papers
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Monilethrix Treated with Minoxidil
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Frontal fibrosing alopecia: a review of eleven patients
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Molecular Genetics of Human Hair Diseases
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- p63: a crucial player in epithelial stemness regulation
- Validation of TrichoScan® technology as a fully-automated tool for evaluation of hair growth parameters