These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 12384772)

  • 1. 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; 2002 Oct; 111(4-5):314-22. PubMed ID: 12384772
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; Endo F; Kitano A; Matsuda I
    J Clin Invest; 1990 Jul; 86(1):351-5. PubMed ID: 2365824
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients.
    Zanaboni G; Dyne KM; Rossi A; Monafo V; Cetta G
    Haematologica; 1994; 79(1):13-8. PubMed ID: 15378943
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations.
    Lupi A; Tenni R; Rossi A; Cetta G; Forlino A
    Amino Acids; 2008 Nov; 35(4):739-52. PubMed ID: 18340504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growth.
    Dolenga M; Hechtman P
    Pediatr Res; 1992 Oct; 32(4):479-82. PubMed ID: 1437403
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of prolidase as an enzyme participating in the metabolism of collagen.
    Pałka JA
    Rocz Akad Med Bialymst; 1996; 41(2):149-60. PubMed ID: 9020526
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide.
    Tanoue A; Endo F; Akaboshi I; Oono T; Arata J; Matsuda I
    J Clin Invest; 1991 Apr; 87(4):1171-6. PubMed ID: 2010534
    [TBL] [Abstract][Full Text] [Related]  

  • 8. N-benzyloxycarbonyl-L-proline: an in vitro and in vivo inhibitor of prolidase.
    Lupi A; Rossi A; Vaghi P; Gallanti A; Cetta G; Forlino A
    Biochim Biophys Acta; 2005 Jun; 1744(2):157-63. PubMed ID: 15878628
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intracellular delivery of liposome-encapsulated prolidase in cultured fibroblasts from prolidase-deficient patients.
    Perugini P; Hassan K; Genta I; Modena T; Pavanetto F; Cetta G; Zanone C; Iadarola P; Asti A; Conti B
    J Control Release; 2005 Jan; 102(1):181-90. PubMed ID: 15653144
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.
    Lupi A; De Riso A; Torre SD; Rossi A; Campari E; Vilarinho L; Cetta G; Forlino A
    J Hum Genet; 2004; 49(9):500-506. PubMed ID: 15309682
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome.
    Hershkovitz T; Hassoun G; Indelman M; Shlush LI; Bergman R; Pollack S; Sprecher E
    Clin Exp Dermatol; 2006 May; 31(3):435-40. PubMed ID: 16681595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies.
    Lupi A; Della Torre S; Campari E; Tenni R; Cetta G; Rossi A; Forlino A
    FEBS J; 2006 Dec; 273(23):5466-78. PubMed ID: 17081196
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biodegradable microspheres for prolidase delivery to human cultured fibroblasts.
    Lupi A; Perugini P; Genta I; Modena T; Conti B; Casado B; Cetta G; Pavanetto F; Iadarola P
    J Pharm Pharmacol; 2004 May; 56(5):597-603. PubMed ID: 15142336
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family.
    Lupi A; Rossi A; Campari E; Pecora F; Lund AM; Elcioglu NH; Gultepe M; Di Rocco M; Cetta G; Forlino A
    J Med Genet; 2006 Dec; 43(12):e58. PubMed ID: 17142620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of prolidase causes a bone phenotype both in human and in mouse.
    Besio R; Maruelli S; Gioia R; Villa I; Grabowski P; Gallagher O; Bishop NJ; Foster S; De Lorenzi E; Colombo R; Diaz JL; Moore-Barton H; Deshpande C; Aydin HI; Tokatli A; Kwiek B; Kasapkara CS; Adisen EO; Gurer MA; Di Rocco M; Phang JM; Gunn TM; Tenni R; Rossi A; Forlino A
    Bone; 2015 Mar; 72():53-64. PubMed ID: 25460580
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis of prolidase (peptidase D) deficiency.
    Endo F; Matsuda I
    Mol Biol Med; 1991 Feb; 8(1):117-27. PubMed ID: 1943683
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer.
    Ikeda K; Tohyama J; Tsujino S; Sato K; Oono T; Arata J; Endo F; Sakuragawa N
    Jpn J Hum Genet; 1997 Sep; 42(3):401-8. PubMed ID: 12503186
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of prolidase activity by nickel causes decreased growth of proline auxotrophic CHO cells.
    Miltyk W; Surazynski A; Kasprzak KS; Fivash MJ; Buzard GS; Phang JM
    J Cell Biochem; 2005 Apr; 94(6):1210-7. PubMed ID: 15696600
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.
    Endo F; Tanoue A; Kitano A; Arata J; Danks DM; Lapière CM; Sei Y; Wadman SK; Matsuda I
    J Clin Invest; 1990 Jan; 85(1):162-9. PubMed ID: 1688567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.