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Research 181–210 of 1000+
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- An Update of Congenital Adrenal Hyperplasia
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Biology and Genetics of Hair
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- The dermatological consequences of obesity
- Biotinidase deficiency characterized by skin and hair findings
- Epidermal expression of receptor for advanced glycation end products (RAGE) is related to inflammation and apoptosis in human skin
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Nano-Enabled CRISPR-Cas Gene Editing for Cancer Therapeutics
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- The Trotter collection: A review of Mildred Trotter's hair research and an update for studies of human variation
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Main Plenary Sessions: Summaries of Papers
- Nonalcoholic fatty liver disease and polycystic ovary syndrome