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

250 related items for PubMed ID: 35947995

  • 1. Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy.
    Nie Z, Wang C, Chen J, Ji Y, Zhang H, Zhao F, Zhou X, Guan MX.
    Hum Mol Genet; 2023 Jan 06; 32(2):231-243. PubMed ID: 35947995
    [Abstract] [Full Text] [Related]

  • 2. Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.
    Chen JR, Chen C, Chen J, Ji Y, Lian Y, Zhang J, Yu J, Li XY, Qu J, Guan MX.
    Hum Mol Genet; 2023 Apr 20; 32(9):1539-1551. PubMed ID: 36611011
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 5. Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Lu Y, Yi Q, Chen M, Xie S, Mao X, Xiao Y, Meng F, Zhang M, Yang R, Guan MX.
    J Biol Chem; 2020 Sep 18; 295(38):13224-13238. PubMed ID: 32723871
    [Abstract] [Full Text] [Related]

  • 6. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Zhang Z, Ji Y, Zhang J, Liang M, Zhao F, Sun YH, Zhang M, Zhou X, Chen Y, Mo JQ, Huang T, Qu J, Guan MX.
    Hum Mol Genet; 2016 Feb 01; 25(3):584-96. PubMed ID: 26647310
    [Abstract] [Full Text] [Related]

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

  • 8. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
    Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, Jiang P, Zhu T, Mo JQ, Huang T, Jiang P, Guan MX.
    Hum Mol Genet; 2019 May 01; 28(9):1515-1529. PubMed ID: 30597069
    [Abstract] [Full Text] [Related]

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

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

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Generation of an induced pluripotent stem cell line from a patient with leber's hereditary optic neuropathy carrying a homoplasmic m.3635G > A mutation in the mitochondrial ND1 gene.
    Ji D, Su X, Hu C, Zhang Z, Wang M, Zou W, Shen L, Liu Y, Liang C, Du Y, Liang D, Cao Y.
    Stem Cell Res; 2022 Aug 01; 63():102858. PubMed ID: 35905669
    [Abstract] [Full Text] [Related]

  • 19. Leber's Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development.
    Karaarslan C.
    Adv Ther; 2019 Dec 01; 36(12):3299-3307. PubMed ID: 31605306
    [Abstract] [Full Text] [Related]

  • 20. A challenging differential diagnosis - Leber's Hereditary Optic Neuropathy.
    Iorga RE, Munteanu-Dănulescu RS, Danielescu C.
    Rom J Ophthalmol; 2024 Dec 01; 68(1):65-71. PubMed ID: 38617721
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.