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Research 361–390 of 1000+
- Table of Contents
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- Prevalence of cervical insufficiency in polycystic ovarian syndrome
- Inhibition of Hair Growth by Testosterone in the Presence of Dermal Papilla Cells from the Frontal Bald Scalp of the Postpubertal Stumptailed Macaque
- Activation of Cilia-Independent Hedgehog/GLI1 Signaling as a Novel Concept for Neuroblastoma Therapy
- Genomic Analysis of Trichotillomania
- Hoxc13 and homologs of mammalian hair keratins are required for the cornification of nuptial pads in Xenopus frogs
- Glycogen phase separation drives macromolecular rearrangement and asymmetric division in E. coli
- The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway
- Facile and Efficient Enzymatic Methods for Harvesting or Removal of Cuticle Cells from Human Hair Shafts
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Lepidoptera Lexicon: Metaphorical Descriptors in Dermatology
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Effect of the Hypoxic Chamber Training Series on Skin Characteristics of Overweight and Obese Women
- Curl pattern classification: A potential tool for communication and risk stratification
- Adipose Tissue‐Derived Exosomes in the Treatment of Lichen Planopilaris: A Case Report
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A Profuse Pipeline of Promising Options