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Research 691–720 of 1000+
- A Novel In Vivo Model for Evaluating Agents that Protect Against Ultraviolet A-induced Photoaging
- Skin tissue engineering
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Apoptosis in Hair and Skin: A Review
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- Current Genetics in Hair Diseases
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Repurposing DPP4-Inhibition to Improve Hair Follicle Activation and Regeneration
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Molecular Mechanisms Regulating Hair Follicle Development
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Genetic Disorders and Defects in Vitamin D Action
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- 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.
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Keloid risk in patients with atopic dermatitis: a nationwide retrospective cohort study in Taiwan
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia