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Research 481–510 of 1000+
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Fibroblasts: Origins, definitions, and functions in health and disease
- Macrophage Related Chronic Inflammation in Non-Healing Wounds
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Role of FGFR2-signaling in the pathogenesis of acne
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Skin tissue engineering
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Radiation Dermatitis: Radiation-Induced Effects on the Structural and Immunological Barrier Function of the Epidermis
- Current Genetics in Hair Diseases
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- 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.
- A newborn presenting with congenital blistering
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Diseases of the Canine Prostate Gland