Citations for
1PEPD
Serum prolidase activity and oxidative status in patients with stage I endometrial cancer.
Arioz DT, Camuzcuoglu H, Toy H, Kurt S, Celik H, Aksoy N.
Int J Gynecol Cancer 19(7):1244-7.PMID: 19823062 2009
2PEPD
Diagnostic value of serum prolidase enzyme activity to predict the liver histological lesions in non-alcoholic fatty liver disease: a surrogate marker to distinguish steatohepatitis from simple steatosis.
Kayadibi H, Gültepe M, Yasar B, Ince AT, Ozcan O, Ipcioglu OM, Kurdas OO, Bolat B, Benek YZ, Guveli H, Atalay S, Ozkara S, Keskin O.
Dig Dis Sci 54(8):1764-71. Epub 2008 Nov 7.PMID: 18989777 2009
3PEPD
The association of serum prolidase activity with the presence and severity of coronary artery disease.
Yildiz A, Demirbag R, Yilmaz R, Gur M, Altiparmak IH, Akyol S, Aksoy N, Ocak AR, Erel O.
Coron Artery Dis 19(5):319-25.PMID: 18607169 2008
4PEPD
Association of prolidase activity, oxidative parameters, and presence of atrial fibrillation in patients with mitral stenosis.
Rabus M, Demirbag R, Yildiz A, Tezcan O, Yilmaz R, Ocak AR, Alp M, Erel O, Aksoy N, Yakut C.
Arch Med Res 39(5):519-24. Epub 2008 Apr 28.PMID: 18514097 2008
5PEPD
Prolidase activity in serum and pleural fluids in patients with tuberculous pleural effusion [correction of effussion].
Ipcioglu OM, Ozcan O, Gultepe M, Deniz O, Akgul EO.
Clin Biochem 41(9):670-5. Epub 2008 Mar 20.PMID: 18387361 2008
6PEPD
Extracellular matrix and HIF-1 signaling: the role of prolidase.
Surazynski A, Donald SP, Cooper SK, Whiteside MA, Salnikow K, Liu Y, Phang JM.
Int J Cancer 122(6):1435-40.PMID: 17999410 2008
7PEPD
Serum prolidase activity in patients with hypertension and its relation with left ventricular hypertrophy.
Demirbag R, Yildiz A, Gur M, Yilmaz R, Elçi K, Aksoy N.
Clin Biochem 40(13-14):1020-5. Epub 2007 Jun 8.PMID: 17604013 2007
8PEPD
A nonsense mutation of PEPD in four Amish children with prolidase deficiency.
Wang H, Kurien BT, Lundgren D, Patel NC, Kaufman KM, Miller DL, Porter AC, D'Souza A, Nye L, Tumbush J, Hupertz V, Kerr DS, Kurono S, Matsumoto H, Scofield RH.
Am J Med Genet A 140(6):580-5. 2006
9PEPD
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts.
Forlino A, Lupi A, Vaghi P, Icaro Cornaglia A, Calligaro A, Campari E, Cetta G.
Hum Genet 111(4-5):314-22. Epub 2002 Aug 14. 2002
10PEPD
FAK-independent regulation of prolidase activity and collagen biosynthesis in MCF-7 cells.
Surazynski A, Palka J.
Folia Histochem Cytobiol 39 Suppl 2:212-3. 2001
11PEPD
A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiency.
Kikuchi S, Tanoue A, Endo F, Wakasugi S, Matsuo N, Tsujimoto G.
J Hum Genet 45(2):102-4. 2000
12PEPD
Expression and molecular analysis of mutations in prolidase deficiency.
Ledoux P, et al.
Am J Hum Genet 59 : 1035-1039. 1996
13PEPD
Four novel PEPD alleles causing prolidase deficiency.
Ledoux P, et al.
Am J Hum Genet 54 : 1014-1021. 1994
14PEPD
Molecular basis of prolidase (peptidase D) deficiency.
Endo F, et al.
Mol Biol Med 8 : 117-127. 1991
15PEPD
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide.
Tanoue A, et al.
J Clin Invest 87 : 1171-1176. 1991
16PEPD
A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cells.
Tanoue A, et al.
J Clin Invest 86 : 351-355. 1990
17PEPD
Primary structure and gene localization of human prolidase.
Endo F, Tanoue A, Nakai H, Hata A, Indo Y, Titani K, Matsuda I.
J Biol Chem 264 : 4476-4481. 1989
18PEPD
Prolidase deficiency : biochemical classification of alleles.
Boright AP, et al.
Am J Hum Genet 44 : 731-740. 1989
19PEPD
New linkage data on chromosome 19 with particular reference to PEPD.
Davis MB, et al.
(HGM9) Cytogenet Cell Genet 46 : 604. 1987
20PEPD
Localization of PEPD to the long arm of chromosome 19.
Davis MB, et al.
Ann Hum Genet 51 : 195-199. 1987
21CYP2@, PEPD
Linkage between the loci for peptidase D and cytochrome P-450 (CYP1) on chromosome 19.
Davis MB.
Ann Hum Genet 51 : 9-12. 1987
22APOC1, APOC2, APOE, C3, LDLR, PEPD, GPI
Regional mapping of human chromosome 19 : Organisation of genes for plasma lipid transport (APOC1,-C2, and -E and LDLR) and the genes C3, PEPD, and GPI.
Lusis AJ, et al.
Proc Natl Acad Sci U S A 83 : 3929-3933. 1986
23GSD2, MAN2B1, PEPD
Further regional localization of the genes for human acid alpha glucosidase (GAA), peptidase D (PEPD), and î-mannosidase (MANB) by somatic cell hybridization.
Martiniuk F, et al.
Hum Genet 69 : 109-111. 1985
24APOC2, PEPD
Linkage between the loci for peptidase D and apolipoprotein CII on chromosome 19.
Ball SP, et al.
Ann Hum Genet 49 : 129-134. 1985
25C3, PEPD, GPI, APOE
Mapping studies with peptidase D (PEPD).
Ball S, et al.
(HGM7) Cytogenet Cell Genet 37 : 411-412. 1984
26C3, FUT2, LE, PEPD, BCAM
Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
Eiberg H, et al.
Clin Genet 24 : 159-170. 1983
27DM1, PEPD
Genetic linkage between the loci for myotonic dystrophy and peptidase D.
O'Brien T, et al.
Ann Hum Genet 47 : 117-121. 1983
28PEPD
Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man.
McAlpine PJ, et al.
Cytogenet Cell Genet 16 : 204-205. 1976
29PEPD
A prolidase deficiency in man with iminopeptiduria.
Powell GF, et al.
Metabolism 23 : 505-513. 1974
30PEPD
A syndrome resembling lathyrism associated with iminodipeptiduria.
Goodman SI, et al.
Am J Med 45 : 52-59. 1968