Connection

GRAEME MARDON to Humans

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

0.123
  1. CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes. Sci Rep. 2015 Feb 10; 5:8366.
    View in: PubMed
    Score: 0.013
  2. Sds22/PP1 links epithelial integrity and tumor suppression via regulation of myosin II and JNK signaling. Oncogene. 2011 Jul 21; 30(29):3248-60.
    View in: PubMed
    Score: 0.010
  3. Signaling in the third dimension: the peripodial epithelium in eye disc development. Dev Dyn. 2009 Sep; 238(9):2139-48.
    View in: PubMed
    Score: 0.009
  4. Whole-mount analysis reveals normal numbers of dopaminergic neurons following misexpression of alpha-Synuclein in Drosophila. Genesis. 2005 Apr; 41(4):154-9.
    View in: PubMed
    Score: 0.007
  5. Identification of a Clade-Specific HLA-C*03:02 CTL Epitope GY9 Derived from the HIV-1 p17 Matrix Protein. Int J Mol Sci. 2024 Sep 06; 25(17).
    View in: PubMed
    Score: 0.006
  6. Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress. Development. 2004 May; 131(9):2183-94.
    View in: PubMed
    Score: 0.006
  7. Long-term non-progression and risk factors for disease progression among children living with HIV in Botswana and Uganda: A retrospective cohort study. Int J Infect Dis. 2024 Feb; 139:132-140.
    View in: PubMed
    Score: 0.006
  8. Dbest1, a Drosophila homolog of human Bestrophin, is not required for viability or photoreceptor integrity. Genesis. 2001 Nov; 31(3):130-6.
    View in: PubMed
    Score: 0.005
  9. Characterization of mouse Dach2, a homologue of Drosophila dachshund. Mech Dev. 2001 Apr; 102(1-2):169-79.
    View in: PubMed
    Score: 0.005
  10. High-depth African genomes inform human migration and health. Nature. 2020 10; 586(7831):741-748.
    View in: PubMed
    Score: 0.005
  11. Mouse Dach, a homologue of Drosophila dachshund, is expressed in the developing retina, brain and limbs. Dev Genes Evol. 1999 Sep; 209(9):526-36.
    View in: PubMed
    Score: 0.004
  12. Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana. Am J Hum Genet. 2018 05 03; 102(5):731-743.
    View in: PubMed
    Score: 0.004
  13. The collaborative African genomics network training program: a trainee perspective on training the next generation of African scientists. Genet Med. 2017 07; 19(7):826-833.
    View in: PubMed
    Score: 0.004
  14. A Genetic Mechanism for Convergent Skin Lightening during Recent Human Evolution. Mol Biol Evol. 2016 05; 33(5):1177-87.
    View in: PubMed
    Score: 0.003
  15. The endogenous cell-fate factor dachshund restrains prostate epithelial cell migration via repression of cytokine secretion via a cxcl signaling module. Cancer Res. 2015 May 15; 75(10):1992-2004.
    View in: PubMed
    Score: 0.003
  16. Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina. Hum Mol Genet. 2015 Mar 15; 24(6):1584-601.
    View in: PubMed
    Score: 0.003
  17. Research capacity. Enabling the genomic revolution in Africa. Science. 2014 Jun 20; 344(6190):1346-8.
    View in: PubMed
    Score: 0.003
  18. Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nat Genet. 2012 Sep; 44(9):1035-9.
    View in: PubMed
    Score: 0.003
  19. Exome capture sequencing identifies a novel mutation in BBS4. Mol Vis. 2011; 17:3529-40.
    View in: PubMed
    Score: 0.003
  20. Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Hum Mutat. 2011 Dec; 32(12):1450-9.
    View in: PubMed
    Score: 0.003
  21. The enhancer of trithorax and polycomb gene Caf1/p55 is essential for cell survival and patterning in Drosophila development. Development. 2011 May; 138(10):1957-66.
    View in: PubMed
    Score: 0.002
  22. Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis. Hum Genet. 2011 Mar; 129(3):319-27.
    View in: PubMed
    Score: 0.002
  23. Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers. Mol Cell Biol. 1990 Feb; 10(2):681-8.
    View in: PubMed
    Score: 0.002
  24. The Dachshund gene in development and hormone-responsive tumorigenesis. Trends Endocrinol Metab. 2010 Jan; 21(1):41-9.
    View in: PubMed
    Score: 0.002
  25. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. Am J Hum Genet. 2009 Mar; 84(3):380-7.
    View in: PubMed
    Score: 0.002
  26. Mutation survey of known LCA genes and loci in the Saudi Arabian population. Invest Ophthalmol Vis Sci. 2009 Mar; 50(3):1336-43.
    View in: PubMed
    Score: 0.002
  27. Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes. Mech Dev. 2002 Feb; 111(1-2):75-87.
    View in: PubMed
    Score: 0.001
  28. Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. Genes Dev. 1999 Dec 15; 13(24):3231-43.
    View in: PubMed
    Score: 0.001
  29. Putative transcription activator with alternative isoforms encoded by human ZFX gene. Nature. 1989 Dec 07; 342(6250):708-11.
    View in: PubMed
    Score: 0.001
  30. The sex-determining region of the human Y chromosome encodes a finger protein. Cell. 1987 Dec 24; 51(6):1091-104.
    View in: PubMed
    Score: 0.000
  31. Isolation of duplicated human c-src genes located on chromosomes 1 and 20. Mol Cell Biol. 1985 Apr; 5(4):831-8.
    View in: PubMed
    Score: 0.000
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.