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Research 91–120 of 159
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Biomedical applications of organoids in genetic diseases
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- The Flavonol Quercitrin Hinders GSK3 Activity and Potentiates the Wnt/β-Catenin Signaling Pathway
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Skin Development and Disease: A Molecular Perspective
- A rare case of woolly hair with unusual associations
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Collodion baby case series: the success of oral retinoic acid
- Current Genetics in Hair Diseases
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Calcium blockers protect against sensory epithelial damage and hearing loss in Cx26-cKO mice
- Abstract 21: Preoperative Versus Postoperative Language Specialization in Infants with Sagittal Craniosynostosis: An ERP Study
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Molecular Basis of Hereditary Hair Diseases
- Connexin mutations in human disease
- Woolly hair generalizado: caso clínico e revisão da literatura
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Skin disease in pregnancy
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates