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 *

169 related articles for article (PubMed ID: 37762220)

  • 1. Conditional Deletion of
    Cao G; Sun C; Shen H; Qu D; Shen C; Lu H
    Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37762220
    [No Abstract]   [Full Text] [Related]  

  • 2. Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome.
    Wilpert NM; Marguet F; Maillard C; Guimiot F; Martinovic J; Drunat S; Attié-Bitach T; Razavi F; Tessier A; Capri Y; Laquerrière A; Bahi-Buisson N
    Eur J Med Genet; 2021 Sep; 64(9):104282. PubMed ID: 34284163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Conditional Deletion of Foxg1 Alleviates Demyelination and Facilitates Remyelination via the Wnt Signaling Pathway in Cuprizone-Induced Demyelinated Mice.
    Dong F; Liu D; Jiang F; Liu Y; Wu X; Qu X; Liu J; Chen Y; Fan H; Yao R
    Neurosci Bull; 2021 Jan; 37(1):15-30. PubMed ID: 33015737
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Oligodendrocyte precursor cell-intrinsic effect of Rheb1 controls differentiation and mediates mTORC1-dependent myelination in brain.
    Zou Y; Jiang W; Wang J; Li Z; Zhang J; Bu J; Zou J; Zhou L; Yu S; Cui Y; Yang W; Luo L; Lu QR; Liu Y; Chen M; Worley PF; Xiao B
    J Neurosci; 2014 Nov; 34(47):15764-78. PubMed ID: 25411504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Involvement of Mitochondrial Dysfunction in
    Bjerregaard VA; Levy AM; Batz MS; Salehi R; Hildonen M; Hammer TB; Møller RS; Desler C; Tümer Z
    Genes (Basel); 2023 Jan; 14(2):. PubMed ID: 36833172
    [No Abstract]   [Full Text] [Related]  

  • 6. Conditional Deletion of the L-Type Calcium Channel Cav1.2 in Oligodendrocyte Progenitor Cells Affects Postnatal Myelination in Mice.
    Cheli VT; Santiago González DA; Namgyal Lama T; Spreuer V; Handley V; Murphy GG; Paez PM
    J Neurosci; 2016 Oct; 36(42):10853-10869. PubMed ID: 27798140
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PLP1-Targeting Antisense Oligonucleotides Improve FOXG1 Syndrome Mice.
    Tan DCS; Jung S; Deng Y; Morey N; Chan G; Bongers A; Ke YD; Ittner LM; Delerue F
    Int J Mol Sci; 2024 Oct; 25(19):. PubMed ID: 39409184
    [TBL] [Abstract][Full Text] [Related]  

  • 8. mTORC2 Loss in Oligodendrocyte Progenitor Cells Results in Regional Hypomyelination in the Central Nervous System.
    Dahl KD; Almeida AR; Hathaway HA; Bourne J; Brown TL; Finseth LT; Wood TL; Macklin WB
    J Neurosci; 2023 Jan; 43(4):540-558. PubMed ID: 36460463
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypoplastic hippocampus in atypical Rett syndrome with a novel FOXG1 mutation.
    Harada K; Yamamoto M; Konishi Y; Koyano K; Takahashi S; Namba M; Kusaka T
    Brain Dev; 2018 Jan; 40(1):49-52. PubMed ID: 28781028
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
    Ellaway CJ; Ho G; Bettella E; Knapman A; Collins F; Hackett A; McKenzie F; Darmanian A; Peters GB; Fagan K; Christodoulou J
    Eur J Hum Genet; 2013 May; 21(5):522-7. PubMed ID: 22968132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome.
    Das DK; Jadhav V; Ghattargi VC; Udani V
    Gene; 2014 Mar; 538(1):109-12. PubMed ID: 24412290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Impaired Postnatal Myelination in a Conditional Knockout Mouse for the Ferritin Heavy Chain in Oligodendroglial Cells.
    Wan R; Cheli VT; Santiago-González DA; Rosenblum SL; Wan Q; Paez PM
    J Neurosci; 2020 Sep; 40(40):7609-7624. PubMed ID: 32868463
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sox2 Is Essential for Oligodendroglial Proliferation and Differentiation during Postnatal Brain Myelination and CNS Remyelination.
    Zhang S; Zhu X; Gui X; Croteau C; Song L; Xu J; Wang A; Bannerman P; Guo F
    J Neurosci; 2018 Feb; 38(7):1802-1820. PubMed ID: 29335358
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Foxg1 has an essential role in postnatal development of the dentate gyrus.
    Tian C; Gong Y; Yang Y; Shen W; Wang K; Liu J; Xu B; Zhao J; Zhao C
    J Neurosci; 2012 Feb; 32(9):2931-49. PubMed ID: 22378868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of FOXG1 in the postnatal development and survival of mouse cochlear hair cells.
    He Z; Fang Q; Li H; Shao B; Zhang Y; Zhang Y; Han X; Guo R; Cheng C; Guo L; Shi L; Li A; Yu C; Kong W; Zhao C; Gao X; Chai R
    Neuropharmacology; 2019 Jan; 144():43-57. PubMed ID: 30336149
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant.
    Bahi-Buisson N; Nectoux J; Girard B; Van Esch H; De Ravel T; Boddaert N; Plouin P; Rio M; Fichou Y; Chelly J; Bienvenu T
    Neurogenetics; 2010 May; 11(2):241-9. PubMed ID: 19806373
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A FOXG1 mutation in a boy with congenital variant of Rett syndrome.
    Le Guen T; Bahi-Buisson N; Nectoux J; Boddaert N; Fichou Y; Diebold B; Desguerre I; Raqbi F; Daire VC; Chelly J; Bienvenu T
    Neurogenetics; 2011 Feb; 12(1):1-8. PubMed ID: 20734096
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leukemia inhibitory factor regulates the timing of oligodendrocyte development and myelination in the postnatal optic nerve.
    Ishibashi T; Lee PR; Baba H; Fields RD
    J Neurosci Res; 2009 Nov; 87(15):3343-55. PubMed ID: 19598242
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.
    Goubau C; Devriendt K; Van der Aa N; Crepel A; Wieczorek D; Kleefstra T; Willemsen MH; Rauch A; Tzschach A; de Ravel T; Leemans P; Van Geet C; Buyse G; Freson K
    Eur J Hum Genet; 2013 Dec; 21(12):1349-55. PubMed ID: 23632790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.
    Allou L; Lambert L; Amsallem D; Bieth E; Edery P; Destrée A; Rivier F; Amor D; Thompson E; Nicholl J; Harbord M; Nemos C; Saunier A; Moustaïne A; Vigouroux A; Jonveaux P; Philippe C
    Eur J Hum Genet; 2012 Dec; 20(12):1216-23. PubMed ID: 22739344
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.