Connection

ASHUTOSH PANDEY to Humans

This is a "connection" page, showing publications ASHUTOSH PANDEY has written about Humans.
Connection Strength

0.147
  1. NGLY1 Deficiency, a Congenital Disorder of Deglycosylation: From Disease Gene Function to Pathophysiology. Cells. 2022 03 29; 11(7).
    View in: PubMed
    Score: 0.020
  2. Tracing the NGLY1 footprints: insights from Drosophila. J Biochem. 2022 Feb 21; 171(2):153-160.
    View in: PubMed
    Score: 0.020
  3. Multifaceted regulation of Notch signaling by glycosylation. Glycobiology. 2021 01 09; 31(1):8-28.
    View in: PubMed
    Score: 0.019
  4. Sensitized genetic backgrounds reveal differential roles for EGF repeat xylosyltransferases in Drosophila Notch signaling. Glycobiology. 2018 11 01; 28(11):849-859.
    View in: PubMed
    Score: 0.016
  5. An evolutionarily conserved role for the aryl hydrocarbon receptor in the regulation of movement. PLoS Genet. 2014 Sep; 10(9):e1004673.
    View in: PubMed
    Score: 0.012
  6. Functionally enigmatic genes: a case study of the brain ignorome. PLoS One. 2014; 9(2):e88889.
    View in: PubMed
    Score: 0.012
  7. Environmental Chemical-Induced Reactive Oxygen Species Generation and Immunotoxicity: A Comprehensive Review. Antioxid Redox Signal. 2024 04; 40(10-12):691-714.
    View in: PubMed
    Score: 0.006
  8. Child Neurology: Progressive Cerebellar Atrophy and Retinal Dystrophy: Clues to an Ultrarare ACO2-Related Neurometabolic Diagnosis. Neurology. 2023 10 10; 101(15):e1567-e1571.
    View in: PubMed
    Score: 0.006
  9. Immunoinformatics based designing a multi-epitope vaccine against pathogenic Chandipura vesiculovirus. J Cell Biochem. 2022 02; 123(2):322-346.
    View in: PubMed
    Score: 0.005
  10. A conserved role for AMP-activated protein kinase in NGLY1 deficiency. PLoS Genet. 2020 12; 16(12):e1009258.
    View in: PubMed
    Score: 0.005
  11. Exome sequencing and characterization of 49,960 individuals in the UK Biobank. Nature. 2020 10; 586(7831):749-756.
    View in: PubMed
    Score: 0.005
  12. BET Bromodomain Inhibitor iBET151 Impedes Human ILC2 Activation and Prevents Experimental Allergic Lung Inflammation. Front Immunol. 2019; 10:678.
    View in: PubMed
    Score: 0.004
  13. Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy. Hum Mol Genet. 2019 01 15; 28(2):290-306.
    View in: PubMed
    Score: 0.004
  14. Acetylation and phosphorylation of human TFAM regulate TFAM-DNA interactions via contrasting mechanisms. Nucleic Acids Res. 2018 04 20; 46(7):3633-3642.
    View in: PubMed
    Score: 0.004
  15. In Inflamed Intestinal Tissues and Epithelial Cells, Interleukin 22?Signaling Increases Expression of H19 Long Noncoding RNA, Which Promotes Mucosal Regeneration. Gastroenterology. 2018 07; 155(1):144-155.
    View in: PubMed
    Score: 0.004
  16. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Nat Commun. 2017 07 12; 8:16015.
    View in: PubMed
    Score: 0.004
  17. Joint mouse-human phenome-wide association to test gene function and disease risk. Nat Commun. 2016 Feb 02; 7:10464.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.