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OpenAlex topic

RNA regulation and disease

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 1,541 works 11 author topics

Works

1,541 works

  1. Genome wide analysis reveals characteristics of off target sites bound by the Cas9 endonuclease 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.9%

    No abstract yet.

  2. Characterization of human disease phenotypes associated with mutations in TREX1 RNASEH2A RNASEH2B RNASEH2C SAMHD1 ADAR and IFIH1 2015
    YÖKSİS SJR Q2 JCR Q3 OpenAlex top 1% OpenAlex 99.7%

    Aicardi-Goutières syndrome is an inflammatory disease occurring due to mutations in any of TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR or IFIH1. We report on 374 patients from 299 families with mutations in these seven genes. Most patients conformed to one of two fairly stereotyped clinical profiles; either exhi…

  3. CRISPR C-to-G base editors for inducing targeted DNA transversions in human cells. 2021
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.8%

    No abstract yet.

  4. Cocaine- and amphetamine-regulated transcript peptide immunohistochemical localization in the rat brain 1998
    OpenAlex top 10% OpenAlex 98.0%

    Cocaine- and amphetamine-regulated transcript (CART) is a brain-enriched mRNA with a protein product(s) that is a candidate brain neurotransmitter. We have developed antisera to CART peptide fragment 106-129 and have demonstrated specific immunoreactivity (IR) at the light microscopic level throughout the brain, spina…

  5. CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration. 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%

    No abstract yet.

  6. CLP1 founder mutation links trna splicing and maturation to cerebellar development and neurodegeneration 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.9%

    No abstract yet.

  7. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%

    No abstract yet.

  8. LIN28 Binds Messenger RNAs at GGAGA Motifs and Regulates Splicing Factor Abundance 2012
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.0%

    No abstract yet.

  9. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%

    No abstract yet.

  10. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%

    No abstract yet.

  11. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.8%

    No abstract yet.

  12. A Polymorphism in IRF4 Affects Human Pigmentation through a Tyrosinase Dependent MITF TFAP2A Pathway 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.1%

    No abstract yet.

Academicians

11 academicians