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Research 331–360 of 1000+
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Clinical Snippets
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- New developments in the molecular treatment of ichthyosis: review of the literature
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Local circadian clock gates cell cycle progression of transient amplifying cells during regenerative hair cycling
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- The nude gene and the skin
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Boron deficiency responses in maize (<i>Zea mays</i> L.) roots
- Hair & Cutaneous Development
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
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- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Types I and II Keratin Intermediate Filaments
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Promotion of homology-directed DNA repair by polyamines
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature