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Items: 16

1.

PEPD is a pivotal regulator of p53 tumor suppressor.

Yang L, Li Y, Bhattacharya A, Zhang Y.

Nat Commun. 2017 Dec 12;8(1):2052. doi: 10.1038/s41467-017-02097-9.

2.

The Many Faces of the Flavivirus NS5 Protein in Antagonism of Type I Interferon Signaling.

Best SM.

J Virol. 2017 Jan 18;91(3). pii: e01970-16. doi: 10.1128/JVI.01970-16. Print 2017 Feb 1. Review.

3.

Prolidase Deficiency in a Mexican-American Patient Identified by Array CGH Reveals a Novel and the Largest PEPD Gene Deletion.

Hintze JP, Kirby A, Torti E, Batanian JR.

Mol Syndromol. 2016 May;7(2):80-6. doi: 10.1159/000445397. Epub 2016 Apr 14.

4.

Dual inhibition of ErbB1 and ErbB2 in cancer by recombinant human prolidase mutant hPEPD-G278D.

Yang L, Li Y, Bhattacharya A, Zhang Y.

Oncotarget. 2016 Jul 5;7(27):42340-42352. doi: 10.18632/oncotarget.9851.

5.

A plasma proteolysis pathway comprising blood coagulation proteases.

Yang L, Li Y, Bhattacharya A, Zhang Y.

Oncotarget. 2016 Jul 5;7(27):40919-40938. doi: 10.18632/oncotarget.7261.

6.

Flavivirus Antagonism of Type I Interferon Signaling Reveals Prolidase as a Regulator of IFNAR1 Surface Expression.

Lubick KJ, Robertson SJ, McNally KL, Freedman BA, Rasmussen AL, Taylor RT, Walts AD, Tsuruda S, Sakai M, Ishizuka M, Boer EF, Foster EC, Chiramel AI, Addison CB, Green R, Kastner DL, Katze MG, Holland SM, Forlino A, Freeman AF, Boehm M, Yoshii K, Best SM.

Cell Host Microbe. 2015 Jul 8;18(1):61-74. doi: 10.1016/j.chom.2015.06.007.

7.

Prolidase activity in chronic plaque psoriasis patients.

Sürücü HA, Aksoy N, Ozgöztas O, Sezen H, Yesilova Y, Turan E.

Postepy Dermatol Alergol. 2015 Apr;32(2):82-7. doi: 10.5114/pdia.2015.48049. Epub 2015 Mar 30.

8.

Enalapril stimulates collagen biosynthesis through prolidase-dependent mechanism in cultured fibroblasts.

Szoka L, Karna E, Morka RP, Palka JA.

Naunyn Schmiedebergs Arch Pharmacol. 2015 Jun;388(6):677-83. doi: 10.1007/s00210-015-1114-5. Epub 2015 Mar 17.

9.

Structural basis of substrate selectivity of E. coli prolidase.

Weaver J, Watts T, Li P, Rye HS.

PLoS One. 2014 Oct 29;9(10):e111531. doi: 10.1371/journal.pone.0111531. eCollection 2014.

10.

Brain morphological defects in prolidase deficient mice: first report.

Insolia V, Piccolini VM.

Eur J Histochem. 2014 Sep 17;58(3):2417. doi: 10.4081/ejh.2014.2417.

11.

Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue.

Besio R, Gioia R, Cossu F, Monzani E, Nicolis S, Cucca L, Profumo A, Casella L, Tenni R, Bolognesi M, Rossi A, Forlino A.

PLoS One. 2013;8(3):e58792. doi: 10.1371/journal.pone.0058792. Epub 2013 Mar 13.

12.

Partial Rescue of Biochemical Parameters After Hematopoietic Stem Cell Transplantation in a Patient with Prolidase Deficiency Due to Two Novel PEPD Mutations.

Caselli D, Cimaz R, Besio R, Rossi A, De Lorenzi E, Colombo R, Cantarini L, Riva S, Spada M, Forlino A, Aricò M.

JIMD Rep. 2012;3:71-7. doi: 10.1007/8904_2011_62. Epub 2011 Sep 27.

13.

Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature review.

Butbul Aviel Y, Mandel H, Avitan Hersh E, Bergman R, Adiv OE, Luder A, Brik R.

Pediatr Rheumatol Online J. 2012 Jun 22;10(1):18. doi: 10.1186/1546-0096-10-18.

14.

A snapshot of the Ixodes scapularis degradome.

Mulenga A, Erikson K.

Gene. 2011 Aug 15;482(1-2):78-93. doi: 10.1016/j.gene.2011.04.008. Epub 2011 Apr 28.

15.

Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.

Lillvis JH, Kyo Y, Tromp G, Lenk GM, Li M, Lu Q, Igo RP Jr, Sakalihasan N, Ferrell RE, Schworer CM, Gatalica Z, Land S, Kuivaniemi H.

BMC Med Genet. 2011 Jan 19;12:14. doi: 10.1186/1471-2350-12-14.

16.

Arginine metabolism and nutrition in growth, health and disease.

Wu G, Bazer FW, Davis TA, Kim SW, Li P, Marc Rhoads J, Carey Satterfield M, Smith SB, Spencer TE, Yin Y.

Amino Acids. 2009 May;37(1):153-68. doi: 10.1007/s00726-008-0210-y. Epub 2008 Nov 23. Review.

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