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Research 841–870 of 1000+
- Matrix Metalloproteinase-19 Expression in Normal and Diseased Skin: Dysregulation by Epidermal Proliferation
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Transgender Competent Provider
- A Comment on Coronavirus Disease 2019 and the Hair
- Thrombospondin-1 Plays a Critical Role in the Induction of Hair Follicle Involution and Vascular Regression During the Catagen Phase
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Milestones in Photocarcinogenesis
- The Molecular Biology of the Vitamin D Receptor
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Chronic overlapping pain conditions and nociplastic pain
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Hair and Scalp Variation Related to Gender
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Syndromes of Severe Insulin Resistance (SSIRs)
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- HAIR AND SYSTEMATIC DISEASE