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Connection

David Simpson to Mutation

This is a "connection" page, showing publications David Simpson has written about Mutation.

 
Connection Strength
 
 
 
0.210
 
  1. Zhao L, Wang F, Wang H, Li Y, Alexander S, Wang K, Willoughby CE, Zaneveld JE, Jiang L, Soens ZT, Earle P, Simpson D, Silvestri G, Chen R. Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland. Hum Genet. 2015 Feb; 134(2):217-30.
    View in: PubMed
    Score: 0.058
  2. Simpson D, Crosby RM, Skopek TR. A method for specific cloning and sequencing of human hprt cDNA for mutation analysis. Biochem Biophys Res Commun. 1988 Feb 29; 151(1):487-92.
    View in: PubMed
    Score: 0.036
  3. Burger JA, Robak T, Demirkan F, Bairey O, Moreno C, Simpson D, Munir T, Stevens DA, Dai S, Cheung LWK, Kwei K, Lal I, Hsu E, Kipps TJ, Tedeschi A. Up to 6.5 years (median 4 years) of follow-up of first-line ibrutinib in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma and high-risk genomic features: integrated analysis of two phase 3 studies. Leuk Lymphoma. 2022 06; 63(6):1375-1386.
    View in: PubMed
    Score: 0.024
  4. Manna P, Hung ST, Mukherjee S, Friis P, Simpson DM, Lo MN, Palmer AE, Jimenez R. Directed evolution of excited state lifetime and brightness in FusionRed using a microfluidic sorter. Integr Biol (Camb). 2018 09 17; 10(9):516-526.
    View in: PubMed
    Score: 0.019
  5. S?rensen MB, M?ller M, Skerritt J, Simpson D. Hordein promoter methylation and transcriptional activity in wild-type and mutant barley endosperm. Mol Gen Genet. 1996 Apr 10; 250(6):750-60.
    View in: PubMed
    Score: 0.016
  6. Choi JY, Hightower GK, Wong JK, Heaton R, Woods S, Grant I, Marcotte TD, Ellis RJ, Letendre SL, Collier AC, Marra CM, Clifford DB, Gelman BB, McArthur JC, Morgello S, Simpson DM, McCutchan JA, Richman DD, Smith DM. Genetic features of cerebrospinal fluid-derived subtype B HIV-1 tat. J Neurovirol. 2012 Apr; 18(2):81-90.
    View in: PubMed
    Score: 0.012
  7. Recio L, Simpson D, Cochrane J, Liber H, Skopek TR. Molecular analysis of hprt mutants induced by 2-cyanoethylene oxide in human lymphoblastoid cells. Mutat Res. 1990 Nov; 242(3):195-208.
    View in: PubMed
    Score: 0.011
  8. Recio L, Cochrane J, Simpson D, Skopek TR, O'Neill JP, Nicklas JA, Albertini RJ. DNA sequence analysis of in vivo hprt mutation in human T lymphocytes. Mutagenesis. 1990 Sep; 5(5):505-10.
    View in: PubMed
    Score: 0.011
  9. Skopek TR, Recio L, Simpson D, Dallaire L, Melancon SB, Ogier H, O'Neill JP, Falta MT, Nicklas JA, Albertini RJ. Molecular analyses of a Lesch-Nyhan syndrome mutation (hprtMontreal) by use of T-lymphocyte cultures. Hum Genet. 1990 Jun; 85(1):111-6.
    View in: PubMed
    Score: 0.011
  10. Wang Y, Chen W, Simpson DM, Elion EA. Cdc24 regulates nuclear shuttling and recruitment of the Ste5 scaffold to a heterotrimeric G protein in Saccharomyces cerevisiae. J Biol Chem. 2005 Apr 01; 280(13):13084-96.
    View in: PubMed
    Score: 0.007
  11. Flotho A, Simpson DM, Qi M, Elion EA. Localized feedback phosphorylation of Ste5p scaffold by associated MAPK cascade. J Biol Chem. 2004 Nov 05; 279(45):47391-401.
    View in: PubMed
    Score: 0.007
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.

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