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Research 121–150 of 730
- Co-expression of PADI isoforms during progenitor differentiation enables functional diversity
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Plant elicitor Peptides regulate root hair development in Arabidopsis
- E-Poster
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- Biotin and biotinidase deficiency
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Genetic Disorders and Defects in Vitamin D Action
- A Receptor-Like Kinase Mediates Ammonium Homeostasis and Is Important for the Polar Growth of Root Hairs in<i>Arabidopsis</i>
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Ichthyosis with confetti: clinics, molecular genetics and management
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Cytokine Targeted Therapeutics for Alopecia Areata: Lessons from Atopic Dermatitis and Other Inflammatory Skin Diseases
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Antioxidation, Anti-Inflammation, and Regulation of SRD5A Gene Expression of Oryza sativa cv. Bue Bang 3 CMU Husk and Bran Extracts as Androgenetic Alopecia Molecular Treatment Substances
- Current Genetics in Hair Diseases
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
- Modulating immune responses in alopecia: therapeutic insights and potential targets of antisense oligonucleotides
- Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Congenital Adrenal Hyperplasia
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>