27 results on '"Javadiyan, Shari"'
Search Results
2. An In Vitro Study Evaluating the Safety of Mesalazine on Human Nasoepithelial Cells
3. The effect of chemical and structural modifiers on the haemostatic process and cytotoxicity of the beta-chitin patch
4. Hydrocortisone metabolism by Staphylococcus: Effects on anti‐inflammatory and antimicrobial action.
5. Hydrocortisone metabolism by Staphylococcus: effects on anti‐inflammatory and antimicrobial action
6. Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse
7. Angiopoietin-1 is required for Schlemm's canal development in mice and humans
8. In Vitro safety and anti‐bacterial efficacy assessment of Acriflavine
9. Green synthesized colloidal silver is devoid of toxic effects on primary human nasal epithelial cells in vitro
10. Investigation of Kappa Carrageenan's muco‐adhesive, antibacterial, and anti‐biofilm properties
11. Acoustic drug delivery to the maxillary sinus
12. Investigation of Kappa Carrageenan's muco‐adhesive, antibacterial, and anti‐biofilm properties.
13. Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
14. Association between viral infection and increased mucosal eosinophils and CD8 + CD103 + T cells in chronic rhinosinusitis
15. Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
16. Additional file 1: Table S1. of Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (AymĂŠ-Gripp syndrome)
17. Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka
18. Congenital glaucoma with anterior segment dysgenesis in individuals with biallelicCPAMD8variants
19. MOESM1 of Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
20. High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
21. Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
22. Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract
23. Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma.
24. Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract
25. Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
26. Association between viral infection and increased mucosal eosinophils and CD8+CD103+ T cells in chronic rhinosinusitis.
27. High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia.
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