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42 Matching Annotations

Apr 2025
www.biorxiv.org www.biorxiv.org

Investigation of the Role of the LC3 Conjugation System in Autophagy for Human Reward System Reactivity

1
1. scibot 03 Apr 2025
  
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  RRID:SCR_002338
  
  DOI: 10.1101/2025.03.26.645396
  
  Resource: dbSNP (RRID:SCR_002338)
  
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biorxiv.org/content/10.1101/2025.03.26.645396v1
Jan 2025
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

Predisposition footprints in the somatic genome of Wilms tumours

1
1. scibot 24 Jan 2025
  
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  RRID:SCR_002338
  
  DOI: 10.1158/2159-8290.CD-24-0878
  
  Resource: dbSNP (RRID:SCR_002338)
  
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pmc.ncbi.nlm.nih.gov/articles/PMC7617291/
Dec 2024
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

Modeling Drug Responses and Evolutionary Dynamics using Patient-Derived Xenografts Reveals Precision Medicine Strategies for Triple Negative Breast Cancer

1
1. scibot 21 Dec 2024
  
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  SCR_002338
  
  DOI: 10.1158/0008-5472.CAN-24-1703
  
  Resource: dbSNP (RRID:SCR_002338)
  
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pmc.ncbi.nlm.nih.gov/articles/PMC7617242/
Nov 2024
52.53.155.43 52.53.155.43

can-24-1703-html.html

1
1. scibot 14 Nov 2024
  
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  SCR_002338
  
  DOI: 10.1158/0008-5472.can-24-1703
  
  Resource: dbSNP (RRID:SCR_002338)
  
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52.53.155.43/8b203bbc7fbd88b2067024854eff5a07e6929833/can-24-1703-html.html
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

SMARTER-database: a tool to integrate SNP array datasets for sheep and goat breeds

1
1. scibot 07 Nov 2024
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.46471/gigabyte.139
  
  Resource: dbSNP (RRID:SCR_002338)
  
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pmc.ncbi.nlm.nih.gov/articles/PMC11519891/
Jul 2024
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study

1
1. scibot 02 Jul 2024
  
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  RRID:SCR_002338
  
  DOI: 10.1158/2767-9764.CRC-24-0026
  
  Resource: dbSNP (RRID:SCR_002338)
  
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ncbi.nlm.nih.gov/pmc/articles/PMC11210444/
Jun 2024
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

MONET: a database for prediction of neoantigens derived from microsatellite loci

1
1. scibot 09 Jun 2024
  
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  RRID:SCR_002338
  
  DOI: 10.3389/fimmu.2024.1394593
  
  Resource: dbSNP (RRID:SCR_002338)
  
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ncbi.nlm.nih.gov/pmc/articles/PMC11148240/
May 2024
aacrjournals.org aacrjournals.org

Negative hyperselection of resistance mutations for panitumumab maintenance in RAS wild-type metastatic colorectal cancer (PanaMa phase II trial, AIO KRK 0212)

1
1. scibot 23 May 2024
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-23-3023
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @abever99
  
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  DOI:10.1158/1078-0432.CCR-23-3023 RRID:SCR_002338
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aacrjournals.org/clincancerres/article/30/7/1256/741834/Negative-Hyperselection-of-Resistance-Mutations
Feb 2024
aacrjournals.org aacrjournals.org

Absence of BTK, BCL2, and PLCG2 Mutations in Chronic Lymphocytic Leukemia Relapsing after First-Line Treatment with Fixed-Duration Ibrutinib plus Venetoclax

3
1. scibot 23 Feb 2024
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-22-3934
  
  Resource: dbSNP (RRID:SCR_002338)
  
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2. scibot 23 Feb 2024
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-22-3934
  
  Resource: dbSNP (RRID:SCR_002338)
  
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3. scibot 03 Feb 2024
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-22-3934
  
  Resource: dbSNP (RRID:SCR_002338)
  
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aacrjournals.org/clincancerres/article/30/3/498/733548/Absence-of-BTK-BCL2-and-PLCG2-Mutations-in-Chronic
Dec 2023
dx.doi.org dx.doi.org

Genetic Predictors of Ibrutinib-Related Cardiovascular Side Effects in Patients with Chronic Lymphocytic Leukemia

1
1. scibot 09 Dec 2023
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-23-0421
  
  Resource: dbSNP (RRID:SCR_002338)
  
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dx.doi.org/10.1158/1078-0432.CCR-23-0421
52.53.155.43 52.53.155.43

ccr-23-0421-html.html

1
1. scibot 01 Dec 2023
  
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  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.ccr-23-0421
  
  Resource: dbSNP (RRID:SCR_002338)
  
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52.53.155.43/c24147616d5f2329d3280c85e26c941ba165dc03/ccr-23-0421-html.html
Oct 2023
52.53.155.43 52.53.155.43

ccr-23-0421-html.html

1
1. scibot 07 Oct 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.ccr-23-0421
  
  Resource: dbSNP (RRID:SCR_002338)
  
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52.53.155.43/c24147616d5f2329d3280c85e26c941ba165dc03/ccr-23-0421-html.html
Jun 2023
aacrjournals.org aacrjournals.org

Enhanced glutaminolysis drives hypoxia-induced chemoresistance in pancreatic cancer

1
1. scibot 03 Jun 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/0008-5472.CAN-22-2045
  
  Resource: dbSNP (RRID:SCR_002338)
  
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aacrjournals.org/cancerres/article/83/5/735/716680/Enhanced-Glutaminolysis-Drives-Hypoxia-Induced
May 2023
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Mutational Landscape of CEBPA in Mexican Pediatric Acute Myeloid Leukemia Patients: Prognostic Implications

2
1. scibot 05 May 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.3389/fped.2022.899742
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
  SciCrunch record: RRID:SCR_002338
  
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  RRID:SCR_002338
2. scibot 05 May 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.3389/fped.2022.899742
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
  SciCrunch record: RRID:SCR_002338
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9367218/
Mar 2023
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Association study between polymorphisms in DNA methylation-related genes and testicular germ cell tumor risk

1
1. scibot 05 Mar 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/1055-9965.EPI-22-0123
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9444936/
Feb 2023
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
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1002/mgg3.2146
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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onlinelibrary.wiley.com/doi/10.1002/mgg3.2146
Jan 2023
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Circulating Tumor DNA in Stage III Colorectal Cancer, beyond Minimal Residual Disease Detection, toward Assessment of Adjuvant Therapy Efficacy and Clinical Behavior of Recurrences

1
1. scibot 12 Jan 2023
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/1078-0432.CCR-21-2404
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9401484/
Nov 2022
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Phase I trial of ribociclib with platinum chemotherapy in ovarian cancer

1
1. scibot 24 Nov 2022
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1172/jci.insight.160573
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9675476/
Sep 2022
www.nature.com www.nature.com

ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP

1
1. scibot 24 Sep 2022
  
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  RRID:SCR_002338
  
  DOI: 10.1038/s41598-022-20343-z
  
  Resource: dbSNP (RRID:SCR_002338)
  
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nature.com/articles/s41598-022-20343-z
Aug 2022
www.sciencedirect.com www.sciencedirect.com

Protocol to identify host-viral protein interactions between coagulation-related proteins and their genetic variants with SARS-CoV-2 proteins

1
1. scibot 27 Aug 2022
  
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  RRID:SCR_002338
  
  DOI: 10.1016/j.xpro.2022.101648
  
  Resource: dbSNP (RRID:SCR_002338)
  
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sciencedirect.com/science/article/pii/S2666166722005287
Jul 2022
52.53.155.43 52.53.155.43

epi-22-0123-html.html

1
1. scibot 29 Jul 2022
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/1055-9965.EPI-22-0123
  
  Resource: dbSNP (RRID:SCR_002338)
  
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52.53.155.43/3de3cb90d6c0869d24f8e6633a22fe84eaf377d7/epi-22-0123-html.html
May 2022
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
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.46471/gigabyte.51
  
  Resource: dbSNP (RRID:SCR_002338)
  
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gigabytejournal.com/articles/51
Apr 2022
journals.physiology.org journals.physiology.org

Whole genome sequencing identifies a deletion mutation in the unknown-functional KCNG2 from familial sick sinus syndrome

1
1. scibot 29 Apr 2022
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1152/physiolgenomics.00132.2021
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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journals.physiology.org/doi/full/10.1152/physiolgenomics.00132.2021
Nov 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Pharmacogenomics characterization of the MDM2 inhibitor MI-773 reveals candidate tumours and predictive biomarkers

1
1. scibot 05 Nov 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1038/s41698-021-00235-7
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8553758/
Oct 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

1
1. scibot 02 Oct 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.7554/eLife.68610
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8476128/
Aug 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Gene mutations in a Han Chinese Alzheimer's disease cohort

1
1. scibot 11 Aug 2021
  
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  SCR_002338
  
  DOI: 10.1002/brb3.1180
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC6346667/
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Studying immunotherapy resistance in a melanoma autologous humanized mouse xenograft.

1
1. scibot 06 Aug 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/1541-7786.MCR-20-0686
  
  Resource: dbSNP (RRID:SCR_002338)
  
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ncbi.nlm.nih.gov/pmc/articles/PMC7864867/
Jul 2021
onlinelibrary.wiley.com onlinelibrary.wiley.com

Gene mutations in a Han Chinese Alzheimer's disease cohort

1
1. scibot 30 Jul 2021
  
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  SCR_002338
  
  DOI: 10.1002/brb3.1180
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
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onlinelibrary.wiley.com/doi/full/10.1002/brb3.1180
onlinelibrary.wiley.com onlinelibrary.wiley.com

Untitled document

1
1. scibot 29 Jul 2021
  
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  RRID:SCR_002338
  
  DOI: 10.1002/jcb.27636
  
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onlinelibrary.wiley.com/doi/full/10.1002/jcb.27636
europepmc.org europepmc.org

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

2
1. scibot 29 Jul 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.7554/eLife.30490
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
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  RRID:SCR_002338 RRIDCUR:Duplicate RRIDCUR:Validated
2. scibot 29 Jul 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.7554/eLife.30490
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
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  RRID:SCR_002338 RRIDCUR:Validated
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europepmc.org/articles/PMC5764568/
May 2021
cancerres.aacrjournals.org cancerres.aacrjournals.org

Bladder tumor subtype commitment occurs in carcinoma in-situ driven by key signaling pathways including ECM remodeling

1
1. scibot 10 May 2021
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1158/0008-5472.CAN-20-2336
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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cancerres.aacrjournals.org/content/81/6/1552
Mar 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Triple-Negative Essential Thrombocythemia: Clinical-Pathological and Molecular Features. A Single-Center Cohort Study

1
1. scibot 31 Mar 2021
  
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  RRID:SCR_002338
  
  DOI: 10.3389/fonc.2021.637116
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @scibot
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8006378/
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
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1093/hmg/ddaa268
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:SCR_002338
  
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  RRIDCUR:Validated RRID:SCR_002338
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URL

academic.oup.com/hmg/article/29/22/3679/6035190
Sep 2020
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract

1
1. scibot 26 Sep 2020
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1371/journal.pone.0227859
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
  SciCrunch record: RRID:SCR_002338
  
  What is this?
  
  RRID:SCR_002338 RRIDCUR:Validated
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RRIDCUR:Validated

RRID:SCR_002338

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scibot

URL

ncbi.nlm.nih.gov/pmc/articles/PMC6959596/
Jan 2020
www.sciencedirect.com www.sciencedirect.com

Genome-wide Analyses of Chromatin State in Human Mast Cells Reveal Molecular Drivers and Mediators of Allergic and Inflammatory Diseases

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1016/j.immuni.2019.09.021
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:SCR_002338
  
  What is this?
  
  RRID:SCR_002338 RRIDCUR:Validated
Visit annotations in context

Tags

RRIDCUR:Validated

RRID:SCR_002338

Annotators

scibot

URL

sciencedirect.com/science/article/pii/S1074761319304170
www.sciencedirect.com www.sciencedirect.com

A Patient-Derived Glioblastoma Organoid Model and Biobank Recapitulates Inter- and Intra-tumoral Heterogeneity

1
1. scibot 13 Jan 2020
  
  in Public
  
  RRID:SCR_002338
  
  DOI: 10.1016/j.cell.2019.11.036
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @ethanbadger
  
  SciCrunch record: RRID:SCR_002338
  
  What is this?
  
  RRID:SCR_002338 RRIDCUR:Validated
Visit annotations in context

Tags

RRIDCUR:Validated

RRID:SCR_002338

Annotators

scibot

URL

sciencedirect.com/science/article/pii/S0092867419313212
onlinelibrary.wiley.com onlinelibrary.wiley.com

Gene mutations in a Han Chinese Alzheimer's disease cohort

1
1. scibot 13 Jan 2020
  
  in Public
  
  SCR_002338
  
  DOI: 10.1002/brb3.1180
  
  Resource: dbSNP (RRID:SCR_002338)
  
  Curator: @evieth
  
  SciCrunch record: SCR_002338
  
  What is this?
  
  RRID:SCR_002338 RRIDCUR:Validated
Visit annotations in context

Tags

RRIDCUR:Validated

RRID:SCR_002338

Annotators

scibot

URL

onlinelibrary.wiley.com/doi/full/10.1002/brb3.1180
Apr 2019
www.sciencedirect.com www.sciencedirect.com

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

1
1. scibot 05 Apr 2019
  
  in Public
  
  nif-0000-02734
  
  Resource used:
  
  (dbSNP, RRID:SCR_002338)
  
  SciCrunch record: RRID:nif-0000-02734
  
  Alternate resolvers: SciCrunch xml N2T identifiers.org
  
  What is this?
  
  RRID:SCR_002338
Visit annotations in context

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RRID:SCR_002338

Annotators

scibot

URL

sciencedirect.com/science/article/pii/S0896627315008375