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Research 451–480 of 1000+
- Dermal white adipose tissue: Development and impact on hair follicles, skin defense, and fibrosis
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- 664 Understanding the pathogenesis of seborrhea-like dermatitis in the Mpzl3 knockout mice
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- 136 Physiological function of Krox20 (Egr2) in epithelial stem cells
- LB999 Role of transcription factor Ovol2 in skin epithelial regeneration and repair
- Analysis of Sonic Hedgehog signalling pathway gene expression in Basal Cell Carcinoma and in GLII induced systems
- BMP signaling in the control of skin development and hair follicle growth
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- A kindred with mutant IKAROS and autoimmunity
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Case report on premature hair graying treated with Melitane 5% and oral hair supplements
- Rapid thawing enhances tissue destruction in a mouse model of cutaneous cryoablation: Insights into oxidative stress and neutrophil activation
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours
- WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of vitamin D receptor mutations in the development of alopecia
- Targeting of Smoothened for therapeutic gain
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- 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.
- Role of the vitamin D receptor in hair follicle biology