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Research 31–60 of 1000+
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- 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
- Short communication: Clinical evaluation of pea sprout extract in the treatment of hair loss
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Formation of regulator/target gene relationships during evolution
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Evolution of Techniques in Hair Transplantation: A 12-Year Perspective
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Evaluation of ischemia-modified albumin level and parameters related with oxidative stress in early onset androgenetic alopecia
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Skin aging: mechanisms, evaluation, and rejuvenation
- A different approach to PCOS: evaluation of spermiogram results in male patients with a family history of PCOS
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Spatiotemporal Expression Characterization of KRTAP6 Family Genes and Its Effect on Wool Traits
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures