Connection

Sherine Chan to Humans

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

0.135
  1. Inherited mitochondrial genomic instability and chemical exposures. Toxicology. 2017 11 01; 391:75-83.
    View in: PubMed
    Score: 0.023
  2. The cellular and molecular progression of mitochondrial dysfunction induced by 2,4-dinitrophenol in developing zebrafish embryos. Differentiation. 2015 Mar-Apr; 89(3-4):51-69.
    View in: PubMed
    Score: 0.019
  3. De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome. Mitochondrion. 2009 Sep; 9(5):340-5.
    View in: PubMed
    Score: 0.013
  4. Functional analysis of mutant mitochondrial DNA polymerase proteins involved in human disease. Methods Mol Biol. 2009; 554:59-72.
    View in: PubMed
    Score: 0.013
  5. DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations. Biochim Biophys Acta. 2009 May; 1787(5):312-9.
    View in: PubMed
    Score: 0.012
  6. Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders. Hum Mol Genet. 2006 Dec 01; 15(23):3473-83.
    View in: PubMed
    Score: 0.011
  7. Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a patient with Alpers syndrome. DNA Repair (Amst). 2005 Dec 08; 4(12):1381-9.
    View in: PubMed
    Score: 0.010
  8. The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit. J Biol Chem. 2005 Sep 09; 280(36):31341-6.
    View in: PubMed
    Score: 0.010
  9. A sensitive assay for the measurement of serum chondroitin sulfate 3B3(-) epitope levels in human rheumatic diseases. Clin Exp Rheumatol. 2001 Sep-Oct; 19(5):533-40.
    View in: PubMed
    Score: 0.008
  10. Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency. Hum Mol Genet. 2014 Jul 01; 23(13):3596-606.
    View in: PubMed
    Score: 0.004
  11. Mitochondrial disorders of DNA polymerase ? dysfunction: from anatomic to molecular pathology diagnosis. Arch Pathol Lab Med. 2011 Jul; 135(7):925-34.
    View in: PubMed
    Score: 0.004
  12. Disease mutations in the human mitochondrial DNA polymerase thumb subdomain impart severe defects in mitochondrial DNA replication. J Biol Chem. 2009 Jul 17; 284(29):19501-10.
    View in: PubMed
    Score: 0.003
  13. Molecular diagnosis of Alpers syndrome. J Hepatol. 2006 Jul; 45(1):108-16.
    View in: PubMed
    Score: 0.003
  14. Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase gamma. Lab Invest. 2007 Apr; 87(4):326-35.
    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.