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

128 related items for PubMed ID: 35526388

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 3. Generation of a human embryonic stem cell line (WAe009-A-43) carrying a Long QT syndrome related mutation in KCNH2 gene.
    Wu X, Zhao Y, Wang X.
    Stem Cell Res; 2020 Oct; 48():101976. PubMed ID: 32911324
    [Abstract] [Full Text] [Related]

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

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

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Generation of patient-specific induced pluripotent stem cell lines with Type 2 Long QT Syndrome and the KCNH2 c.379C > T pathogenic variant.
    Goual L, Bounasri E, Vincenti M, Amédro P, Desprat R, Bernex F, Lemaitre JM, Pasquié JL, Lacampagne A, Thireau J, Meli AC.
    Stem Cell Res; 2023 Oct; 72():103192. PubMed ID: 37660555
    [Abstract] [Full Text] [Related]

  • 9. Generation of a human embryonic stem cell line WAe009-A-79 carrying a long QT syndrome mutation in KCNQ1.
    Wang H, Guo T, Lan F.
    Stem Cell Res; 2023 Aug; 70():103119. PubMed ID: 37244124
    [Abstract] [Full Text] [Related]

  • 10. The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2.
    Mura M, Mehta A, Ramachandra CJ, Zappatore R, Pisano F, Ciuffreda MC, Barbaccia V, Crotti L, Schwartz PJ, Shim W, Gnecchi M.
    Int J Cardiol; 2017 Aug 01; 240():367-371. PubMed ID: 28433559
    [Abstract] [Full Text] [Related]

  • 11. Generation and characterization of an induced pluripotent stem cell (iPSC) line (NUIGi003-A) from a long QT syndrome type 2 (LQT2) patient harbouring the KCNH2 c.2464G>A pathogenic variant.
    Ge N, Liu M, Krawczyk J, McInerney V, Ward D, Shen S, O'Brien T, Prendiville T.
    Stem Cell Res; 2020 Dec 01; 49():101997. PubMed ID: 33002718
    [Abstract] [Full Text] [Related]

  • 12. Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes.
    O'Hare BJ, John Kim CS, Hamrick SK, Ye D, Tester DJ, Ackerman MJ.
    Circ Genom Precis Med; 2020 Oct 01; 13(5):466-475. PubMed ID: 32940533
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients.
    Ono M, Burgess DE, Schroder EA, Elayi CS, Anderson CL, January CT, Sun B, Immadisetty K, Kekenes-Huskey PM, Delisle BP.
    Biomolecules; 2020 Aug 04; 10(8):. PubMed ID: 32759882
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2.
    Fatima A, Ivanyuk D, Herms S, Heilmann-Heimbach S, O'Shea O, Chapman C, Izsvák Z, Farr M, Hescheler J, Šarić T.
    Stem Cell Res; 2016 Mar 04; 16(2):304-7. PubMed ID: 27345990
    [Abstract] [Full Text] [Related]

  • 17. The Advantages, Challenges, and Future of Human-Induced Pluripotent Stem Cell Lines in Type 2 Long QT Syndrome.
    Cai D, Zheng Z, Jin X, Fu Y, Cen L, Ye J, Song Y, Lian J.
    J Cardiovasc Transl Res; 2023 Feb 04; 16(1):209-220. PubMed ID: 35976484
    [Abstract] [Full Text] [Related]

  • 18. Establishment of a human-induced pluripotent stem cell line, KSCBi014-A, from a long QT syndrome type 2 patient harboring a KCNH2 mutation.
    Lee Y, Koo SK, Kim JH.
    Stem Cell Res; 2021 Dec 04; 57():102570. PubMed ID: 34678663
    [Abstract] [Full Text] [Related]

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

  • 20. A Novel Mutation in the KCNH2 Gene Associatedwith Long QT Syndrome: A Case Report.
    Zha K, Ye Q.
    Ann Clin Lab Sci; 2021 Mar 04; 51(2):258-261. PubMed ID: 33941567
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.