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1. Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia

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

3. SARS-CoV-2 ORF3A interacts with the Clic-like chloride channel-1 (CLCC1) and triggers an unfolded protein response

4. Changes in DNA methylation hallmark alterations in chromatin accessibility and gene expression for eye lens differentiation

5. A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts

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

7. Retinal Development and Pathophysiology in Kcnj13 Knockout Mice

8. Autophagy Requirements for Eye Lens Differentiation and Transparency

9. Molecular Genetic Analysis of Ukrainian Families with Congenital Cataracts

10. Hierarchies of evidence applied to lifestyle Medicine (HEALM): introduction of a strength-of-evidence approach based on a methodological systematic review

11. Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression

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

14. A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa

17. FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

21. SARS-CoV-2 ORF3A interacts with the Clic-like chloride channel-1 (CLCC1) and triggers an unfolded protein response.

24. A Mouse Model with Ablated Asparaginase and Isoaspartyl Peptidase 1 (Asrgl1) Develops Early Onset Retinal Degeneration (RD) Recapitulating the Human Phenotype

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

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

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

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

31. Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3

33. Congenital and Inherited Cataracts

36. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.

46. A mutation in IFT43 causes non-syndromic recessive retinal degeneration

47. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani FamiliesPakistani RP Study

48. Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy

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