17 Matching Annotations
  1. Nov 2024
  2. 52.53.155.43 52.53.155.43
    ccr-24-1240-html.html
    1
    1. scibot 14 Nov 2024
      RRID:SCR_007000

      DOI: 10.1158/1078-0432.ccr-24-1240

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
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    52.53.155.43/6cf3ca03fe9336b8c2f71d4e78c72374e9cc1cef/ccr-24-1240-html.html
  3. Nov 2023
  4. aacrjournals.org aacrjournals.org
    Integrative genomic analyses identify lncRNA regulatory networks across pediatric leukemias and solid tumors
    1
    1. scibot 10 Nov 2023
      RRID:SCR_007000

      DOI: 10.1158/0008-5472.CAN-22-3186

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

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      RRID:SCR_007000
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    aacrjournals.org/cancerres/article/83/20/3462/729497/Integrative-Genomic-Analyses-Identify-LncRNA
  5. Oct 2023
  6. 52.53.155.43 52.53.155.43
    can-22-3186-html.html
    1
    1. scibot 07 Oct 2023
      RRID:SCR_007000

      DOI: 10.1158/0008-5472.can-22-3186

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

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      RRID:SCR_007000
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    52.53.155.43/f31f36f9b40930b6ccd28ff367973b288930c09e/can-22-3186-html.html
  7. Sep 2023
  8. 52.53.155.43 52.53.155.43
    can-22-3186-html.html
    1
    1. scibot 22 Sep 2023
      RRID:SCR_007000

      DOI: 10.1158/0008-5472.can-22-3186

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

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      RRID:SCR_007000
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    52.53.155.43/f31f36f9b40930b6ccd28ff367973b288930c09e/can-22-3186-html.html
  9. Feb 2023
  10. onlinelibrary.wiley.com onlinelibrary.wiley.com
    A novel heterozygous ATP1A2 pathogenic variant in a Chinese child with MELAS-like alternating hemiplegia
    1
    1. scibot 08 Feb 2023
      RRID:SCR_007000

      DOI: 10.1002/mgg3.2146

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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    onlinelibrary.wiley.com/doi/10.1002/mgg3.2146
  11. Jun 2022
  12. europepmc.org europepmc.org
    A Role for Gene-Environment Interactions in Autism Spectrum Disorder Is Supported by Variants in Genes Regulating the Effects of Exposure to Xenobiotics
    1
    1. scibot 07 Jun 2022
      RRID:SCR_007000

      DOI: 10.3389/fnins.2022.862315

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
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    europepmc.org/article/PMC/PMC9161282
  13. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    A Role for Gene-Environment Interactions in Autism Spectrum Disorder Is Supported by Variants in Genes Regulating the Effects of Exposure to Xenobiotics
    1
    1. scibot 04 Jun 2022
      RRID:SCR_007000

      DOI: 10.3389/fnins.2022.862315

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

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      RRID:SCR_007000
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    ncbi.nlm.nih.gov/pmc/articles/PMC9161282/
  14. May 2022
  15. gigabytejournal.com gigabytejournal.com
    LT1, an ONT long-read-based assembly scaffolded with Hi-C data and polished with short reads
    1
    1. scibot 10 May 2022
      RRID:SCR_007000

      DOI: 10.46471/gigabyte.51

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
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    gigabytejournal.com/articles/51
  16. Feb 2022
  17. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Solitary Median Maxillary Central Incisor Syndrome: An Exploration of the Pathogenic Mechanism
    2
    1. scibot 11 Feb 2022
      RRID:SCR_007000

      DOI: 10.3389/fgene.2022.780930

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
    2. scibot 10 Feb 2022
      RRID:SCR_007000

      DOI: 10.3389/fgene.2022.780930

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
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    ncbi.nlm.nih.gov/pmc/articles/PMC8819842/
  18. Aug 2021
  19. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Untitled document
    1
    1. scibot 12 Aug 2021
      RRID:SCR_007000

      DOI: 10.1523/JNEUROSCI.3155-16.2017

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

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    ncbi.nlm.nih.gov/pmc/articles/PMC5426185/
  20. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Untitled document
    1
    1. scibot 05 Aug 2021
      SCR_007000

      DOI: 10.1002/brb3.1134

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @scibot

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000
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    ncbi.nlm.nih.gov/pmc/articles/PMC6236233/
  21. Mar 2021
  22. academic.oup.com academic.oup.com
    Germline EGFR variants are over-represented in adolescents and young adults (AYA) with adrenocortical carcinoma
    1
    1. scibot 03 Mar 2021
      RRID:SCR_007000

      DOI: 10.1093/hmg/ddaa268

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @Naa003

      SciCrunch record: RRID:SCR_007000

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      RRID:SCR_007000 RRIDCUR:Validated
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    academic.oup.com/hmg/article/29/22/3679/6035190
  23. Sep 2020
  24. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Novel and de novo point and large microdeletion mutation in PRRT2‐related epilepsy
    1
    1. scibot 15 Sep 2020
      RRID:SCR_007000

      DOI: 10.1002/brb3.1597

      Resource: Database of Genomic Variants (RRID:SCR_007000)

      Curator: @Naa003

      SciCrunch record: RRID:SCR_007000

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      RRIDCUR:Validated RRID:SCR_007000
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    onlinelibrary.wiley.com/doi/10.1002/brb3.1597
  25. Nov 2018
  26. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Untitled document
    1
    1. scibot 05 Nov 2018
      RRID:SCR_007000

      Resource used:

      (Database of Genomic Variants: A curated catalogue of structural variation in the human genome, RRID:SCR_007000)

      SciCrunch record: RRID:SCR_007000

      Alternate resolvers: SciCrunch xml N2T identifiers.org

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      RRID:SCR_007000
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1134
  27. Nov 2017
  28. www.jneurosci.org www.jneurosci.org
    New Repeat Polymorphism in the AKT1 Gene Predicts Striatal Dopamine D2/D3 Receptor Availability and Stimulant-Induced Dopamine Release in the Healthy Human Brain
    1
    1. scibot 09 Nov 2017
      SCR_007000

      Curator: @Zeljana_Babic

      Resource used:

      (Database of Genomic Variants: A curated catalogue of structural variation in the human genome, RRID:SCR_007000)

      SciCrunch record: RRID:SCR_007000

      Alternate resolvers: SciCrunch xml N2T identifiers.org

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      RRID:SCR_007000 RRIDCUR:Validated
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    jneurosci.org/content/37/19/4982
  29. www.jneurosci.org www.jneurosci.org
    Untitled document
    1
    1. scibot 08 Nov 2017
      SCR_007000

      Resource used:

      (Database of Genomic Variants: A curated catalogue of structural variation in the human genome, RRID:SCR_007000)

      SciCrunch record: RRID:SCR_007000

      Alternate resolvers: SciCrunch xml N2T identifiers.org

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      RRID:SCR_007000
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    jneurosci.org/content/37/19/4982.long