43 results on '"J. Fielding"'
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2. The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia
3. SIRT1 Inhibits High Glucose–Induced TXNIP/NLRP3 Inflammasome Activation and Cataract Formation
4. Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism
5. Patterns of Crystallin Gene Expression in Differentiation State Specific Regions of the Embryonic Chicken Lens
6. The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia
7. SIRT1 Inhibits High Glucose–Induced TXNIP/NLRP3 Inflammasome Activation and Cataract Formation
8. Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts
9. LncRNA NEAT1 Recruits SFPQ to Regulate MITF Splicing and Control RPE Cell Proliferation
10. Patterns of Crystallin Gene Expression in Differentiation State Specific Regions of the Embryonic Chicken Lens
11. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families
12. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening
13. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening
14. Congenital Cataracts: Classification and Association With Anterior Segment Abnormalities
15. Hexokinase 1 and Retinitis Pigmentosa: Insights Into the Retina and the Molecule
16. Hexokinase 1 and Retinitis Pigmentosa: Insights Into the Retina and the Molecule
17. Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort
18. GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness
19. Overexpression of Human γC-crystallin 5 bp Duplication Disrupts Lens Morphology in Transgenic Mice
20. Molecular Analysis of Bardet-Biedl Syndrome Families: Report of 21 Novel Mutations in 10 Genes
21. Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort
22. Mutations in ASCC3L1 on 2q11.2 Are Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family
23. Overexpression of Human γC-crystallin 5 bp Duplication Disrupts Lens Morphology in Transgenic Mice
24. Mutations in ASCC3L1 on 2q11.2 Are Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family
25. Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations inCRYAA,CRYGD, andGJA8
26. Analysis of Ocular Hypopigmentation inRab38cht/chtMice
27. Screening of the Eight BBS Genes in Tunisian Families: No Evidence of Triallelism
28. Increased Sensitivity of Amino-Arm Truncated βA3-Crystallin to UV-Light–Induced Photoaggregation
29. Autosomal Recessive Retinitis Pigmentosa Is Associated with Mutations inRP1in Three Consanguineous Pakistani Families
30. Mutations in βB3-Crystallin Associated with Autosomal Recessive Cataract in Two Pakistani Families
31. Methionine Sulfoxide Reductases B1, B2, and B3 Are Present in the Human Lens and Confer Oxidative Stress Resistance to Lens Cells
32. A New Locus for Autosomal Recessive Nuclear Cataract Mapped to Chromosome 19q13 in a Pakistani Family
33. Analysis of Ocular Hypopigmentation inRab38cht/chtMice
34. Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations inCRYAA,CRYGD, andGJA8
35. Genetic Linkage of Snowflake Vitreoretinal Degeneration to Chromosome 2q36
36. A Homozygous Splice Mutation in theHSF4Gene Is Associated with an Autosomal Recessive Congenital Cataract
37. A Nonsense Mutation in the Glucosaminyl (N-acetyl) Transferase 2 Gene (GCNT2): Association with Autosomal Recessive Congenital Cataracts
38. Screening of the Eight BBS Genes in Tunisian Families: No Evidence of Triallelism
39. Autosomal Recessive Retinitis Pigmentosa Is Associated with Mutations inRP1in Three Consanguineous Pakistani Families
40. Mutations in βB3-Crystallin Associated with Autosomal Recessive Cataract in Two Pakistani Families
41. A New Locus for Autosomal Recessive Nuclear Cataract Mapped to Chromosome 19q13 in a Pakistani Family
42. A Homozygous Splice Mutation in theHSF4Gene Is Associated with an Autosomal Recessive Congenital Cataract
43. A Nonsense Mutation in the Glucosaminyl (N-acetyl) Transferase 2 Gene (GCNT2): Association with Autosomal Recessive Congenital Cataracts
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