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 *

131 related articles for article (PubMed ID: 1713629)

  • 21. Long-term correction of ornithine transcarbamylase deficiency by WPRE-mediated overexpression using a helper-dependent adenovirus.
    Mian A; McCormack WM; Mane V; Kleppe S; Ng P; Finegold M; O'Brien WE; Rodgers JR; Beaudet AL; Lee B
    Mol Ther; 2004 Sep; 10(3):492-9. PubMed ID: 15336649
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ultrastructural, immunocytochemical and stereological investigation of hepatocytes in a patient with the mutation of the ornithine transcarbamylase gene.
    Zimmer KP; Matsuda I; Matsuura T; Mori M; Colombo JP; Fahimi HD; Koch HG; Ullrich K; Harms E
    Eur J Cell Biol; 1995 May; 67(1):73-83. PubMed ID: 7641731
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Impact of enzyme activity assay on indication in liver transplantation for ornithine transcarbamylase deficiency.
    Wakiya T; Sanada Y; Urahashi T; Ihara Y; Yamada N; Okada N; Ushijima K; Otomo S; Sakamoto K; Murayama K; Takayanagi M; Hakamada K; Yasuda Y; Mizuta K
    Mol Genet Metab; 2012 Mar; 105(3):404-7. PubMed ID: 22264779
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors.
    Ye X; Robinson MB; Batshaw ML; Furth EE; Smith I; Wilson JM
    J Biol Chem; 1996 Feb; 271(7):3639-46. PubMed ID: 8631974
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Import of rat ornithine transcarbamylase precursor into mitochondria: two-step processing of the leader peptide.
    Sztul ES; Hendrick JP; Kraus JP; Wall D; Kalousek F; Rosenberg LE
    J Cell Biol; 1987 Dec; 105(6 Pt 1):2631-9. PubMed ID: 3693395
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene.
    Hata A; Setoyama C; Shimada K; Takeda E; Kuroda Y; Akaboshi I; Matsuda I
    Am J Hum Genet; 1989 Jul; 45(1):123-7. PubMed ID: 2741942
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation.
    Ogino W; Takeshima Y; Nishiyama A; Okizuka Y; Yagi M; Tsuneishi S; Saiki K; Kugo M; Matsuo M
    Kobe J Med Sci; 2007; 53(5):229-40. PubMed ID: 18204299
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogeny.
    McIntyre P; Graf L; Mercer JF; Wake SA; Hudson P; Hoogenraad N
    DNA; 1985 Apr; 4(2):147-56. PubMed ID: 3838931
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expression of amplified DNA sequences for ornithine transcarbamylase in HeLa cells: arginine residues may be required for mitochondrial import of enzyme precursor.
    Horwich AL; Fenton WA; Firgaira FA; Fox JE; Kolansky D; Mellman IS; Rosenberg LE
    J Cell Biol; 1985 May; 100(5):1515-21. PubMed ID: 3988798
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Biogenesis of ornithine transcarbamylase in spfash mutant mice: two cytoplasmic precursors, one mitochondrial enzyme.
    Rosenberg LE; Kalousek F; Orsulak MD
    Science; 1983 Oct; 222(4622):426-8. PubMed ID: 6623083
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations.
    Giorgi M; Morrone A; Donati MA; Ciani F; Bardelli T; Biasucci G; Zammarchi E
    Hum Mutat; 2000 Apr; 15(4):380-1. PubMed ID: 10737985
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal monitoring in a family at high risk for ornithine transcarbamylase (OTC) deficiency: a new mutation of an A-to-C transversion in position +4 of intron 1 of the OTC gene that is likely to abolish enzyme activity.
    Hoshide R; Matsuura T; Sagara Y; Kubo T; Shimadzu M; Endo F; Matsuda I
    Am J Med Genet; 1996 Aug; 64(3):459-64. PubMed ID: 8862622
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectors.
    Ye X; Zimmer KP; Brown R; Pabin C; Batshaw ML; Wilson JM; Robinson MB
    Hum Gene Ther; 2001 Jun; 12(9):1035-46. PubMed ID: 11399226
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular and biochemical features of the mitochondrial enzyme ornithine transcarbamylase: a possible new role as a signaling factor.
    Díaz-Muñoz M; Hernández-Muñoz R
    Curr Med Chem; 2010; 17(21):2253-60. PubMed ID: 20459380
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.
    Maddalena A; Spence JE; O'Brien WE; Nussbaum RL
    J Clin Invest; 1988 Oct; 82(4):1353-8. PubMed ID: 3170748
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosome.
    Slomski R; Braulke I; Behrend C; Schröder E; Colombo JP; Reiss J
    Hum Genet; 1992 Aug; 89(6):632-4. PubMed ID: 1511981
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Separation of ornithine and lysine activities of the ornithine-transcarbamylase-catalyzed reaction.
    Hommes FA; Eller AG; Scott DF; Carter AL
    Enzyme; 1983; 29(4):271-7. PubMed ID: 6409607
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency.
    Li S; Cai Y; Shi C; Liu M; Liu B; Lin L; Xiao X; Hao H
    Med Sci Monit; 2018 Oct; 24():7431-7437. PubMed ID: 30333473
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Restoration of hepatic cytochrome c oxidase activity and expression with acetyl-L-carnitine treatment in spf mice with an ornithine transcarbamylase deficiency.
    Mawal YR; Rama Rao KV; Qureshi IA
    Biochem Pharmacol; 1998 Jun; 55(11):1853-60. PubMed ID: 9714304
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The spfash mouse: a missense mutation in the ornithine transcarbamylase gene also causes aberrant mRNA splicing.
    Hodges PE; Rosenberg LE
    Proc Natl Acad Sci U S A; 1989 Jun; 86(11):4142-6. PubMed ID: 2471197
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.