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Items: 9


Sequence features governing aggregation or degradation of prion-like proteins.

Cascarina SM, Paul KR, Machihara S, Ross ED.

PLoS Genet. 2018 Jul 13;14(7):e1007517. doi: 10.1371/journal.pgen.1007517. eCollection 2018 Jul.


Manipulating the aggregation activity of human prion-like proteins.

Cascarina SM, Paul KR, Ross ED.

Prion. 2017 Sep 3;11(5):323-331. doi: 10.1080/19336896.2017.1356560.


Effects of Mutations on the Aggregation Propensity of the Human Prion-Like Protein hnRNPA2B1.

Paul KR, Molliex A, Cascarina S, Boncella AE, Taylor JP, Ross ED.

Mol Cell Biol. 2017 Mar 31;37(8). pii: e00652-16. doi: 10.1128/MCB.00652-16. Print 2017 Apr 15.


Controlling the prion propensity of glutamine/asparagine-rich proteins.

Paul KR, Ross ED.

Prion. 2015;9(5):347-54. doi: 10.1080/19336896.2015.1111506.


Generating new prions by targeted mutation or segment duplication.

Paul KR, Hendrich CG, Waechter A, Harman MR, Ross ED.

Proc Natl Acad Sci U S A. 2015 Jul 14;112(28):8584-9. doi: 10.1073/pnas.1501072112. Epub 2015 Jun 22.


Distinct amino acid compositional requirements for formation and maintenance of the [PSI⁺] prion in yeast.

MacLea KS, Paul KR, Ben-Musa Z, Waechter A, Shattuck JE, Gruca M, Ross ED.

Mol Cell Biol. 2015 Mar;35(5):899-911. doi: 10.1128/MCB.01020-14. Epub 2014 Dec 29.


Increasing prion propensity by hydrophobic insertion.

Gonzalez Nelson AC, Paul KR, Petri M, Flores N, Rogge RA, Cascarina SM, Ross ED.

PLoS One. 2014 Feb 20;9(2):e89286. doi: 10.1371/journal.pone.0089286. eCollection 2014.


De novo design of synthetic prion domains.

Toombs JA, Petri M, Paul KR, Kan GY, Ben-Hur A, Ross ED.

Proc Natl Acad Sci U S A. 2012 Apr 24;109(17):6519-24. doi: 10.1073/pnas.1119366109. Epub 2012 Apr 2.


Letter: malabsorption syndrome.

Chakraborty P, Sen D, Paul KR.

J Indian Med Assoc. 1974 May 1;62(9):329. No abstract available.


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