Keyword Analysis & Research: eys


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Keyword CPC PCC Volume Score Length of keyword
eys1.810.37651603

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Keyword CPC PCC Volume Score
eys0.040.4982393

Search Results related to eys on Search Engine

  • Inside EY’s $22 million strategy to get workers back into the office

    hrexecutive.com

    https://hrexecutive.com/inside-eys-22-million-strategy-to-get-workers-back-into-the-office/

    WEBJul 25, 2022 · EY’s fund benefits were instituted in February and, at least for now, ended at the end of the fiscal year—June 30. The benefit was used by a whopping 29,500 EY employees, and reimbursements totaled $22 million. Not only did the fund have a big impact for employees on their willingness to return to office, Giampietro says, but the program is ...

    DA: 7 PA: 66 MOZ Rank: 60

  • Dissecting the role of EYS in retinal degeneration: clinical and

    biomedcentral.com

    https://ojrd.biomedcentral.com/articles/10.1186/s13023-021-01843-z

    WEBMay 17, 2021 · Mutations in the EYS gene are one of the major causes of autosomal recessive retinitis pigmentosa. EYS-retinopathy presents a severe clinical phenotype, and patients currently have no therapeutic options. The progress in personalised medicine and gene and cell therapies hold promise for treating this degenerative disease.

    DA: 21 PA: 84 MOZ Rank: 4

  • Genetic Spectrum of EYS-associated Retinal Disease in a Large …

    nature.com

    https://www.nature.com/articles/s41598-020-62119-3

    WEBMar 26, 2020 · The purpose of this study was to identify pathogenic EYS variants, to determine the clinical/genetic spectrum of EYS-associated retinal disease (EYS-RD), and to discover disease-associated...

    DA: 25 PA: 94 MOZ Rank: 47

  • EYS Mutations Causing Autosomal Recessive Retinitis …

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541311/

    WEBJul 12, 2017 · Mutations in the EYS (eyes shut homolog) gene are a common cause of autosomal recessive (ar) retinitis pigmentosa (RP). Without a mammalian model of human EYS disease, there is limited understanding of details of disease

    DA: 12 PA: 71 MOZ Rank: 5

  • EY's Business Split Plan Gives Partners Seven-Figure Payouts: …

    businessinsider.com

    https://www.businessinsider.com/eys-business-split-plan-gives-partners-seven-figure-payouts-wsj-2022-6

    WEBJun 20, 2022 · EY partners are eyeing multimillion-dollar payouts from a possible split of the corporate giant's consulting and auditing businesses. A plan to split EY's consulting and auditing businesses will ...

    DA: 61 PA: 98 MOZ Rank: 17

  • Genotypic spectrum and phenotype correlations of EYS ... - Nature

    nature.com

    https://www.nature.com/articles/s41433-021-01794-6

    WEBOct 23, 2021 · Results. Thirty-six novel variants, three hot mutations of EYS (30.3%, c.6416G>A, c.6557G>A, c.7492G>C) and one hot region (49.06%, Laminin G domains) were identified. In all, 36.84% of the ...

    DA: 91 PA: 33 MOZ Rank: 76

  • EY login – My EY

    ey.com

    https://login.ey.com/myey/home

    WEBEY login – My EY

    DA: 1 PA: 21 MOZ Rank: 82

  • EYS mutations and implementation of minigene assay for variant

    nih.gov

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032658/

    WEBApr 8, 2021 · We showed that EYS gene is a common cause of arRP in northern Sweden and some of the Swedish patients share an EYS founder allele present in Finnish population. We also illustrated benefits of a minigene assay for demonstration of effects of intronic variants on splicing of the EYS gene in human embryonic kidney cells, HEK293T …

    DA: 36 PA: 10 MOZ Rank: 100

  • EYS Gene - GeneCards | EYS Protein | EYS Antibody

    genecards.org

    https://www.genecards.org/cgi-bin/carddisp.pl?gene=EYS

    WEBApr 3, 2024 · EYS (Eyes Shut Homolog) is a Protein Coding gene. Diseases associated with EYS include Retinitis Pigmentosa 25 and Retinitis Pigmentosa. Gene Ontology (GO) annotations related to this gene include calcium ion binding. An important paralog of this gene is FBLN2.

    DA: 20 PA: 94 MOZ Rank: 39

  • JCI Insight - Phototoxicity avoidance is a potential therapeutic

    jci.org

    https://insight.jci.org/articles/view/174179

    WEB5 days ago · EYS is missing or interrupted in the genome of several mammalian lineages, including the most common animal models: mouse, rat, and guinea pig , and this has made it difficult to investigate EYS-associated retinal dystrophies (EYS-RDs). Thus, zebrafish have been used as an alternative vertebrate model to study the role of the Eys protein.

    DA: 22 PA: 56 MOZ Rank: 47