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 *

124 related articles for article (PubMed ID: 24010702)

  • 21. Sustained correction of OTC deficiency in spf( ash) mice using optimized self-complementary AAV2/8 vectors.
    Wang L; Wang H; Morizono H; Bell P; Jones D; Lin J; McMenamin D; Yu H; Batshaw ML; Wilson JM
    Gene Ther; 2012 Apr; 19(4):404-10. PubMed ID: 21850052
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular characterization of a new mutation E122G of human ornithine transcarbamylase gene].
    Gao H; Li W; Yan ZH; Jiang MH; Rui DR; He YS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):19-22. PubMed ID: 12579493
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Gene therapy for ornithine transcarbamylase deficiency.
    Kiwaki K; Matsuda I
    Acta Paediatr Jpn; 1996 Apr; 38(2):189-92. PubMed ID: 8677801
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel human pathological mutations. Gene symbol: OTC. Disease: ornithine transcarbamylase deficiency.
    Lin HY; Lin HY; Lin SP
    Hum Genet; 2010 Apr; 127(4):475. PubMed ID: 21488237
    [No Abstract]   [Full Text] [Related]  

  • 25. Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
    Koya Y; Shibata M; Senju M; Honma Y; Hiura M; Ishii M; Matsumoto S; Harada M
    Intern Med; 2019 Apr; 58(7):937-942. PubMed ID: 30449781
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Vector-related tumorigenesis not found in ornithine transcarbamylase-deficient mice.
    Koeberl DD
    Mol Ther; 2006 Jul; 14(1):1-2. PubMed ID: 16750655
    [No 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. A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice.
    Yang Y; Wang L; Bell P; McMenamin D; He Z; White J; Yu H; Xu C; Morizono H; Musunuru K; Batshaw ML; Wilson JM
    Nat Biotechnol; 2016 Mar; 34(3):334-8. PubMed ID: 26829317
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia.
    Mohamed S; Hamad MH; Kondkar AA; Abu-Amero KK
    Saudi Med J; 2015 Oct; 36(10):1229-32. PubMed ID: 26446336
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Analysis of clinical features, biochemical analysis and gene mutations in one Chinese pedigree with neonatal-onset ornithine transcarbamylase deficiency].
    Sun WH; Yang Y; Zhang YP; Li XT; Zhang M; Cao Y; Wang Y
    Zhonghua Er Ke Za Zhi; 2011 May; 49(5):356-60. PubMed ID: 21624287
    [TBL] [Abstract][Full Text] [Related]  

  • 31. First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency.
    Ray PF; Gigarel N; Bonnefont JP; Attié T; Hamamah S; Frydman N; Vekemans M; Frydman R; Munnich A
    Prenat Diagn; 2000 Dec; 20(13):1048-54. PubMed ID: 11180228
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation: clinical, biochemical and DNA analyses in a four-generation family.
    Ausems MG; Bakker E; Berger R; Duran M; van Diggelen OP; Keulemans JL; de Valk HW; Kneppers AL; Dorland L; Eskes PF; Beemer FA; Poll-The BT; Smeitink JA
    Am J Med Genet; 1997 Jan; 68(2):236-9. PubMed ID: 9028466
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency.
    Hoshide R; Matsuura T; Komaki S; Koike E; Ueno I; Matsuda I
    J Inherit Metab Dis; 1993; 16(5):857-62. PubMed ID: 8295401
    [No Abstract]   [Full Text] [Related]  

  • 35. Ornithine transcarbamylase deficiency in pregnancy.
    Cordero DR; Baker J; Dorinzi D; Toffle R
    J Inherit Metab Dis; 2005; 28(2):237-40. PubMed ID: 15877212
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH.
    Shchelochkov OA; Li FY; Geraghty MT; Gallagher RC; Van Hove JL; Lichter-Konecki U; Fernhoff PM; Copeland S; Reimschisel T; Cederbaum S; Lee B; Chinault AC; Wong LJ
    Mol Genet Metab; 2009 Mar; 96(3):97-105. PubMed ID: 19138872
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ornithine transcarbamylase deficiency: a novel splice site mutation in a family with meiotic recombination and a new useful SNP for diagnosis.
    Azevedo L; Vilarinho L; Teles EL; Amorim A
    Mol Genet Metab; 2002 May; 76(1):68-70. PubMed ID: 12175783
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Analysis of clinical features, metabolic profiling and gene mutations of patients with ornithine transcarbamylase deficiency].
    Wang Y; Liu X; Wu H; Liu H; Wang C; He X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):148-51. PubMed ID: 24711021
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector.
    Stratford-Perricaudet LD; Levrero M; Chasse JF; Perricaudet M; Briand P
    Hum Gene Ther; 1990; 1(3):241-56. PubMed ID: 2081192
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Clinical and gene mutation analyses of three patients with ornithine carbamoyltransferase deficiency].
    Mo WQ; Liu L; Chen YY; Cheng J; Li XZ; Zhou ZH; Mao XJ; Zhang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):328-31. PubMed ID: 21644234
    [TBL] [Abstract][Full Text] [Related]  

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