19 results on '"TYR"'
Search Results
2. Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
3. Identifying genetic defects in oculocutaneous albinism patients of West Bengal, Eastern India
4. Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights
5. Melatonin inhibits senescence-associated melanin pigmentation through the p53-TYR pathway in human primary melanocytes and the skin of C57BL/6 J mice after UVB irradiation
6. Diagnostic accuracy of a minimal immunohistochemical panel in at/rt molecular subtyping, correlated to dna-methylation profiling
7. Clinical and Molecular Genetic Characteristics of Patients with Oculocutaneous Albinism Type 1
8. NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism
9. Shell Biosynthesis and Pigmentation as Revealed by the Expression of Tyrosinase and Tyrosinase-like Protein Genes in Pacific Oyster (Crassostrea gigas) with Different Shell Colors
10. Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease
11. Thermal stability of the complex of pyrene–β-cyclodextrin dimer with aromatic amino acids
12. Depigmenting effect of argan press-cake extract through the down-regulation of Mitf and melanogenic enzymes expression in B16 murine melanoma cells
13. Identification of a Homozygous Missense Mutation in the TYR Gene in a Chinese Family with OCA1
14. Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations
15. Fluorescence Spectroscopy as a Tool to Unravel the Dynamics of Protein Nanoparticle Formation by Liquid Antisolvent Precipitation
16. Human and cattle remains in a simultaneous deposit in the Hellenistic necropolis of Jal al Bahr in Tyre: Initial investigations
17. ‘ok er hann einhendr’: Tÿr’s Enhanced Functionality
18. A comprehensive study of oculocutaneous albinism type 1 reveals three previously unidentified alleles on the TYR gene
19. Molecular analysis of Korean patients with oculocutaneous albinism
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