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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 39126705

  • 1. Rescue of Scn5a mis-splicing does not improve the structural and functional heart defects of a DM1 heart mouse model.
    Nitschke L, Hu RC, Miller AN, Cooper TA.
    Hum Mol Genet; 2024 Oct 07; 33(20):1789-1799. PubMed ID: 39126705
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. CRISPR -Mediated Expression of the Fetal Scn5a Isoform in Adult Mice Causes Conduction Defects and Arrhythmias.
    Pang PD, Alsina KM, Cao S, Koushik AB, Wehrens XHT, Cooper TA.
    J Am Heart Assoc; 2018 Oct 02; 7(19):e010393. PubMed ID: 30371314
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
    Wahbi K, Algalarrondo V, Bécane HM, Fressart V, Beldjord C, Azibi K, Lazarus A, Berber N, Radvanyi-Hoffman H, Stojkovic T, Béhin A, Laforêt P, Eymard B, Hatem S, Duboc D.
    Arch Cardiovasc Dis; 2013 Dec 02; 106(12):635-43. PubMed ID: 24140416
    [Abstract] [Full Text] [Related]

  • 7. Expression levels of core spliceosomal proteins modulate the MBNL-mediated spliceopathy in DM1.
    Louis JM, Frias JA, Schroader JH, Jones LA, Davey EE, Lennon CD, Chacko J, Cleary JD, Berglund JA, Reddy K.
    Hum Mol Genet; 2024 Nov 05; 33(21):1873-1886. PubMed ID: 39180495
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Reversible cardiac disease features in an inducible CUG repeat RNA-expressing mouse model of myotonic dystrophy.
    Rao AN, Campbell HM, Guan X, Word TA, Wehrens XH, Xia Z, Cooper TA.
    JCI Insight; 2021 Mar 08; 6(5):. PubMed ID: 33497365
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development.
    Michel L, Huguet-Lachon A, Gourdon G.
    PLoS One; 2015 Mar 08; 10(9):e0137620. PubMed ID: 26339785
    [Abstract] [Full Text] [Related]

  • 14. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T, Hayashi H, Suzuki F, Nishiyama Y, Miyamoto Y, Aiba T, Shimizu W, Kimura K.
    J Clin Neurosci; 2020 Apr 08; 74():242-244. PubMed ID: 32063450
    [Abstract] [Full Text] [Related]

  • 15. Reduced cytoplasmic MBNL1 is an early event in a brain-specific mouse model of myotonic dystrophy.
    Wang PY, Lin YM, Wang LH, Kuo TY, Cheng SJ, Wang GS.
    Hum Mol Genet; 2017 Jun 15; 26(12):2247-2257. PubMed ID: 28369378
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Systemic therapy in an RNA toxicity mouse model with an antisense oligonucleotide therapy targeting a non-CUG sequence within the DMPK 3'UTR RNA.
    Yadava RS, Yu Q, Mandal M, Rigo F, Bennett CF, Mahadevan MS.
    Hum Mol Genet; 2020 Jun 03; 29(9):1440-1453. PubMed ID: 32242217
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.