Connection

OGUZ KANCA to Drosophila melanogaster

This is a "connection" page, showing publications OGUZ KANCA has written about Drosophila melanogaster.
Connection Strength

1.453
  1. Raeppli: a whole-tissue labeling tool for live imaging of Drosophila development. Development. 2014 Jan; 141(2):472-80.
    View in: PubMed
    Score: 0.274
  2. Drospondin, a glial glycoprotein with similarities to human Reelin/F-spondin, contributes to Drosophila brain development and function. Proc Natl Acad Sci U S A. 2026 Feb 03; 123(5):e2502307123.
    View in: PubMed
    Score: 0.159
  3. Revealing the nervous system requirements of Alzheimer disease risk genes in Drosophila. Am J Hum Genet. 2025 12 04; 112(12):2870-2887.
    View in: PubMed
    Score: 0.156
  4. Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders. Dis Model Mech. 2025 07 01; 18(7).
    View in: PubMed
    Score: 0.152
  5. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. Am J Hum Genet. 2019 08 01; 105(2):413-424.
    View in: PubMed
    Score: 0.101
  6. A gene-specific T2A-GAL4 library for Drosophila. Elife. 2018 03 22; 7.
    View in: PubMed
    Score: 0.092
  7. Establishment of a Developmental Compartment Requires Interactions between Three Synergistic Cis-regulatory Modules. PLoS Genet. 2015 Oct; 11(10):e1005376.
    View in: PubMed
    Score: 0.078
  8. The Drosophila melanogaster Mutants apblot and apXasta Affect an Essential apterous Wing Enhancer. G3 (Bethesda). 2015 Apr 02; 5(6):1129-43.
    View in: PubMed
    Score: 0.075
  9. Fluorescent fusion protein knockout mediated by anti-GFP nanobody. Nat Struct Mol Biol. 2011 Dec 11; 19(1):117-21.
    View in: PubMed
    Score: 0.060
  10. Two lysosomal genes ATP13A2 and GBA1 interact to drive neurodegeneration. Mol Neurodegener. 2026 Jan 30; 21(1).
    View in: PubMed
    Score: 0.040
  11. Rab4 spatially and functionally converges with Rab7 in the degradative endolysosomal network. Mol Biol Cell. 2026 Mar 01; 37(3):ar18.
    View in: PubMed
    Score: 0.040
  12. Resolving SLC6A1 variable expressivity with deep clinical phenotyping and Drosophila models. HGG Adv. 2026 Jan 15; 7(1):100541.
    View in: PubMed
    Score: 0.039
  13. Functional analysis of pathogenic variants in LAMB1-related leukoencephalopathy reveals genotype-phenotype correlations and suggests its role in glial cells. Hum Mol Genet. 2025 May 17; 34(11):990-999.
    View in: PubMed
    Score: 0.038
  14. C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder. Genet Med. 2025 Jul; 27(7):101429.
    View in: PubMed
    Score: 0.037
  15. Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila. Nat Commun. 2024 Apr 18; 15(1):3326.
    View in: PubMed
    Score: 0.035
  16. Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. Nat Rev Genet. 2024 Jan; 25(1):46-60.
    View in: PubMed
    Score: 0.033
  17. TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. Am J Hum Genet. 2021 09 02; 108(9):1669-1691.
    View in: PubMed
    Score: 0.029
  18. Protein knockouts in living eukaryotes using deGradFP and green fluorescent protein fusion targets. Curr Protoc Protein Sci. 2013 Sep 24; 73:30.2.1-30.2.13.
    View in: PubMed
    Score: 0.017
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.