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2. Congenital and Inherited Cataracts

7. Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism

9. Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two Pedigrees

11. Zonule Associated Gene Variants in Isolated Ectopia Lentis and Glaucoma

12. The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia

18. Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma

22. Truncation mutations in MYRF underlie primary angle closure glaucoma

28. CLCC1 c. 75C>A Mutation in Pakistani Derived Retinitis Pigmentosa Families Likely Originated With a Single Founder Mutation 2,000–5,000 Years Ago

30. Retinal Development and Pathophysiology in Kcnj13 Knockout Mice

34. Lens Biology and Biochemistry

35. Preface

36. Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts

38. Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis

41. A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes

42. Crystallin Genes: Templates for Lens Transparency

43. Vision

44. List of Contributors

46. Whole genome sequencing data of multiple individuals of Pakistani descent

48. MITF protects against oxidative damage-induced retinal degeneration by regulating the NRF2 pathway in the retinal pigment epithelium

50. Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families

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