Ngo L - Search Results

1

Disease-associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex.

Hemming IA, Clément O, Gladwyn-Ng IE, Cullen HD, Ng HL, See HB, Ngo L, Ulgiati D, Pfleger KDG, Agostino M, Heng JI. Hemming IA, et al. Among authors: ngo l. Hum Mutat. 2019 Oct;40(10):1841-1855. doi: 10.1002/humu.23803. Epub 2019 Jul 3. Hum Mutat. 2019. PMID: 31112317 Free article.

2

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation.

Haas MA, Ngo L, Li SS, Schleich S, Qu Z, Vanyai HK, Cullen HD, Cardona-Alberich A, Gladwyn-Ng IE, Pagnamenta AT, Taylor JC, Stewart H, Kini U, Duncan KE, Teleman AA, Keays DA, Heng JI. Haas MA, et al. Among authors: ngo l. Cell Rep. 2016 Jun 7;15(10):2251-2265. doi: 10.1016/j.celrep.2016.04.090. Epub 2016 May 26. Cell Rep. 2016. PMID: 27239039 Free PMC article.

3

Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons.

Gladwyn-Ng I, Huang L, Ngo L, Li SS, Qu Z, Vanyai HK, Cullen HD, Davis JM, Heng JI. Gladwyn-Ng I, et al. Among authors: ngo l. Neural Dev. 2016 Mar 11;11:7. doi: 10.1186/s13064-016-0062-1. Neural Dev. 2016. PMID: 26969432 Free PMC article.

4

Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex.

Gladwyn-Ng IE, Li SS, Qu Z, Davis JM, Ngo L, Haas M, Singer J, Heng JI. Gladwyn-Ng IE, et al. Among authors: ngo l. Neural Dev. 2015 Mar 31;10:9. doi: 10.1186/s13064-015-0032-z. Neural Dev. 2015. PMID: 25888806 Free PMC article.

5

The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome.

Li SS, Qu Z, Haas M, Ngo L, Heo YJ, Kang HJ, Britto JM, Cullen HD, Vanyai HK, Tan SS, Chan-Ling T, Gunnersen JM, Heng JI. Li SS, et al. Among authors: ngo l. Sci Rep. 2016 Jul 11;6:29514. doi: 10.1038/srep29514. Sci Rep. 2016. PMID: 27404227 Free PMC article.

6

Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway.

Edvardson S, Tian G, Cullen H, Vanyai H, Ngo L, Bhat S, Aran A, Daana M, Da'amseh N, Abu-Libdeh B, Cowan NJ, Heng JI, Elpeleg O. Edvardson S, et al. Among authors: ngo l. Hum Mol Genet. 2016 Nov 1;25(21):4635-4648. doi: 10.1093/hmg/ddw292. Hum Mol Genet. 2016. PMID: 28158450 Free PMC article.

7

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

Ngo L, Haas M, Qu Z, Li SS, Zenker J, Teng KS, Gunnersen JM, Breuss M, Habgood M, Keays DA, Heng JI. Ngo L, et al. Hum Mol Genet. 2014 Oct 1;23(19):5147-58. doi: 10.1093/hmg/ddu238. Epub 2014 May 15. Hum Mol Genet. 2014. PMID: 24833723 Free article.

8

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, Xie Y, Robson KJ, Rani DS, Thangaraj K, Clausen T, Chelly J, Cowan NJ, Keays DA. Breuss M, et al. Among authors: ngo l. Cell Rep. 2012 Dec 27;2(6):1554-62. doi: 10.1016/j.celrep.2012.11.017. Epub 2012 Dec 13. Cell Rep. 2012. PMID: 23246003 Free PMC article. Clinical Trial.

9

Nuclear export of RNA: Different sizes, shapes and functions.

Williams T, Ngo LH, Wickramasinghe VO. Williams T, et al. Semin Cell Dev Biol. 2018 Mar;75:70-77. doi: 10.1016/j.semcdb.2017.08.054. Epub 2017 Sep 1. Semin Cell Dev Biol. 2018. PMID: 28866329 Review.

10

Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands.

Verloes A, David A, Ngô L, Bottani A. Verloes A, et al. Among authors: ngo l. J Med Genet. 1995 Aug;32(8):605-11. doi: 10.1136/jmg.32.8.605. J Med Genet. 1995. PMID: 7473651 Free PMC article.

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