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 *

86 related articles for article (PubMed ID: 30242216)

  • 1. mRNA alterations mimic genetic mutations.
    Seton-Rogers S
    Nat Rev Cancer; 2018 Nov; 18(11):664-665. PubMed ID: 30242216
    [No Abstract]   [Full Text] [Related]  

  • 2. Neuronal tissue-specific ribonucleoprotein complex formation on SOD1 mRNA: alterations by ALS SOD1 mutations.
    Ge WW; Leystra-Lantz C; Sanelli TR; McLean J; Wen W; Strong W; Strong MJ
    Neurobiol Dis; 2006 Aug; 23(2):342-50. PubMed ID: 16730180
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nonsense mutations and diminished mRNA levels.
    McIntosh I; Hamosh A; Dietz HC
    Nat Genet; 1993 Jul; 4(3):219. PubMed ID: 8358428
    [No Abstract]   [Full Text] [Related]  

  • 4. Qualitative and quantitative analysis of FBN1 mRNA from 16 patients with Marfan Syndrome.
    Tjeldhorn L; Amundsen SS; Barøy T; Rand-Hendriksen S; Geiran O; Frengen E; Paus B
    BMC Med Genet; 2015 Dec; 16():113. PubMed ID: 26684006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hprt activities and RNA phenotypes in 6-thioguanine resistant human T-lymphocytes.
    Steen AM; Sahlén S; Hou SM; Lambert B
    Mutat Res; 1993 Apr; 286(2):209-15. PubMed ID: 7681532
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Directing ribosomes to a single mRNA species: a method to study ribosomal RNA mutations and their effects on translation of a single messenger in Escherichia coli.
    Hui A; Jhurani P; de Boer HA
    Methods Enzymol; 1987; 153():432-52. PubMed ID: 2828845
    [No Abstract]   [Full Text] [Related]  

  • 7. Nature and mRNA effect of 282 different NF1 point mutations: focus on splicing alterations.
    Pros E; Gómez C; Martín T; Fábregas P; Serra E; Lázaro C
    Hum Mutat; 2008 Sep; 29(9):E173-93. PubMed ID: 18546366
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Insulin receptor messenger ribonucleic acid sequence alterations detected by ribonuclease cleavage in patients with syndromes of insulin resistance.
    Goldstein BJ; Kahn CR
    J Clin Endocrinol Metab; 1989 Jul; 69(1):15-24. PubMed ID: 2732294
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4).
    Abed AA; Günther K; Kraus C; Hohenberger W; Ballhausen WG
    Hum Mutat; 2001 Nov; 18(5):397-410. PubMed ID: 11668633
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lymphocyte mRNA as a resource for detection of mutations and polymorphisms in the CF gene.
    Chalkley G; Harris A
    J Med Genet; 1991 Nov; 28(11):777-80. PubMed ID: 1770535
    [No Abstract]   [Full Text] [Related]  

  • 11. Angiotensinogen messenger RNA stabilization by angiotensin II.
    Klett CP; Printz MP; Bader M; Ganten D; Eggena P
    J Hypertens Suppl; 1996 Dec; 14(5):S25-36. PubMed ID: 9120681
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The influence of codon context on genetic code translation.
    Bossi L; Roth JR
    Nature; 1980 Jul; 286(5769):123-7. PubMed ID: 7402305
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations.
    Sijbrands EJ; Lombardi MP; Westendorp RG; Leuven JA; Meinders AE; Van der Laarse A; Frants RR; Havekes LM; Smelt AH
    Atherosclerosis; 1998 Feb; 136(2):247-54. PubMed ID: 9543095
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New amber mutation in a beta-thalassemic gene with nonmeasurable levels of mutant messenger RNA in vivo.
    Atweh GF; Brickner HE; Zhu XX; Kazazian HH; Forget BG
    J Clin Invest; 1988 Aug; 82(2):557-61. PubMed ID: 3403716
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of point mutations in type I collagen by RNase digestion of RNA/RNA hybrids.
    Grange DK; Gottesman GS; Lewis MB; Marini JC
    Nucleic Acids Res; 1990 Jul; 18(14):4227-36. PubMed ID: 1696002
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of F8 mRNA in haemophilia A patients with silent mutations or presumptive splice site mutations.
    Zimmermann MA; Gehrig A; Oldenburg J; Müller CR; Rost S
    Haemophilia; 2013 Mar; 19(2):310-7. PubMed ID: 23088352
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Messenger RNA processing and its role in diabetes.
    Harries LW
    Diabet Med; 2011 Sep; 28(9):1010-7. PubMed ID: 21699562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A-->G, 2751+2T-->A, 296+1G-->C, 1717-9T-->C-D565G) and one nonsense mutation (E822X) in the CFTR gene.
    Tzetis M; Efthymiadou A; Doudounakis S; Kanavakis E
    Hum Genet; 2001 Dec; 109(6):592-601. PubMed ID: 11810271
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Signs of Selection in Synonymous Sites of the Mitochondrial Cytochrome b Gene of Baikal Oilfish (Comephoridae) by mRNA Secondary Structure Alterations.
    Teterina VI; Mamontov AM; Sukhanova LV; Kirilchik SV
    Biomed Res Int; 2015; 2015():387913. PubMed ID: 26114105
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TERT promoter mutations and TERT mRNA but not FGFR3 mutations are urinary biomarkers in Han Chinese patients with urothelial bladder cancer.
    Wang K; Liu T; Liu C; Meng Y; Yuan X; Liu L; Ge N; Liu J; Wang C; Ren H; Yan K; Hu S; Xu Z; Fan Y; Xu D
    Oncologist; 2015 Mar; 20(3):263-9. PubMed ID: 25657201
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.