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Items: 1 to 20 of 107

1.

A zebrafish model of lethal congenital contracture syndrome 1 reveals Gle1 function in spinal neural precursor survival and motor axon arborization.

Jao LE, Appel B, Wente SR.

Development. 2012 Apr;139(7):1316-26. doi: 10.1242/dev.074344. Epub 2012 Feb 22.

2.

Deficiency in the mRNA export mediator Gle1 impairs Schwann cell development in the zebrafish embryo.

Seytanoglu A, Alsomali NI, Valori CF, McGown A, Kim HR, Ning K, Ramesh T, Sharrack B, Wood JD, Azzouz M.

Neuroscience. 2016 May 13;322:287-97. doi: 10.1016/j.neuroscience.2016.02.039. Epub 2016 Feb 24.

PMID:
26921650
3.

Gle1 functions during mRNA export in an oligomeric complex that is altered in human disease.

Folkmann AW, Collier SE, Zhan X, Aditi, Ohi MD, Wente SR.

Cell. 2013 Oct 24;155(3):582-93. doi: 10.1016/j.cell.2013.09.023. Epub 2013 Oct 24.

4.

Insights into mRNA export-linked molecular mechanisms of human disease through a Gle1 structure-function analysis.

Folkmann AW, Dawson TR, Wente SR.

Adv Biol Regul. 2014 Jan;54:74-91. doi: 10.1016/j.jbior.2013.10.002. Epub 2013 Nov 13. Review.

5.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Levert A, Vidal S, André-Guimont C, Camu W, Bouchard JP, Dupré N, Rouleau GA, Wente SR, Dion PA.

Hum Mol Genet. 2015 Mar 1;24(5):1363-73. doi: 10.1093/hmg/ddu545. Epub 2014 Oct 24.

6.

Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease.

Nousiainen HO, Kestilä M, Pakkasjärvi N, Honkala H, Kuure S, Tallila J, Vuopala K, Ignatius J, Herva R, Peltonen L.

Nat Genet. 2008 Feb;40(2):155-7. doi: 10.1038/ng.2007.65. Epub 2008 Jan 20.

7.

Slow Muscle Precursors Lay Down a Collagen XV Matrix Fingerprint to Guide Motor Axon Navigation.

Guillon E, Bretaud S, Ruggiero F.

J Neurosci. 2016 Mar 2;36(9):2663-76. doi: 10.1523/JNEUROSCI.2847-15.2016.

8.

Nuclear export of the yeast mRNA-binding protein Nab2 is linked to a direct interaction with Gfd1 and to Gle1 function.

Suntharalingam M, Alcázar-Román AR, Wente SR.

J Biol Chem. 2004 Aug 20;279(34):35384-91. Epub 2004 Jun 18.

9.

Expansion of the GLE1-associated arthrogryposis multiplex congenita clinical spectrum.

Smith C, Parboosingh JS, Boycott KM, Bönnemann CG, Mah JK; Care4Rare Canada Consortium., Lamont RE, Micheil Innes A, Bernier FP.

Clin Genet. 2017 Mar;91(3):426-430. doi: 10.1111/cge.12876. Epub 2017 Jan 30.

PMID:
27684565
10.

Knockdown of Pnpla6 protein results in motor neuron defects in zebrafish.

Song Y, Wang M, Mao F, Shao M, Zhao B, Song Z, Shao C, Gong Y.

Dis Model Mech. 2013 Mar;6(2):404-13. doi: 10.1242/dmm.009688. Epub 2012 Sep 20.

11.

Cytoplasmic inositol hexakisphosphate production is sufficient for mediating the Gle1-mRNA export pathway.

Miller AL, Suntharalingam M, Johnson SL, Audhya A, Emr SD, Wente SR.

J Biol Chem. 2004 Dec 3;279(49):51022-32. Epub 2004 Sep 30.

12.

Knockdown of Lingo1b protein promotes myelination and oligodendrocyte differentiation in zebrafish.

Yin W, Hu B.

Exp Neurol. 2014 Jan;251:72-83. doi: 10.1016/j.expneurol.2013.11.012. Epub 2013 Nov 18. Erratum in: Exp Neurol. 2014 Mar;253:111-2.

PMID:
24262204
13.

The SMN binding protein Gemin2 is not involved in motor axon outgrowth.

McWhorter ML, Boon KL, Horan ES, Burghes AH, Beattie CE.

Dev Neurobiol. 2008 Feb 1;68(2):182-94.

14.

Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export.

Weirich CS, Erzberger JP, Flick JS, Berger JM, Thorner J, Weis K.

Nat Cell Biol. 2006 Jul;8(7):668-76. Epub 2006 Jun 18.

PMID:
16783364
15.

Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export.

Alcázar-Román AR, Tran EJ, Guo S, Wente SR.

Nat Cell Biol. 2006 Jul;8(7):711-6. Epub 2006 Jun 18.

PMID:
16783363
16.

Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis.

Carrel TL, McWhorter ML, Workman E, Zhang H, Wolstencroft EC, Lorson C, Bassell GJ, Burghes AH, Beattie CE.

J Neurosci. 2006 Oct 25;26(43):11014-22.

17.

A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function.

Khuchua Z, Yue Z, Batts L, Strauss AW.

Circ Res. 2006 Jul 21;99(2):201-8. Epub 2006 Jun 22.

18.

Protocadherin-18b interacts with Nap1 to control motor axon growth and arborization in zebrafish.

Biswas S, Emond MR, Duy PQ, Hao le T, Beattie CE, Jontes JD.

Mol Biol Cell. 2014 Mar;25(5):633-42. doi: 10.1091/mbc.E13-08-0475. Epub 2013 Dec 26.

19.

Role of the 2 zebrafish survivin genes in vasculo-angiogenesis, neurogenesis, cardiogenesis and hematopoiesis.

Delvaeye M, De Vriese A, Zwerts F, Betz I, Moons M, Autiero M, Conway EM.

BMC Dev Biol. 2009 Mar 26;9:25. doi: 10.1186/1471-213X-9-25.

20.

Zebrafish Parla- and Parlb-deficiency affects dopaminergic neuron patterning and embryonic survival.

Noble S, Ismail A, Godoy R, Xi Y, Ekker M.

J Neurochem. 2012 Jul;122(1):196-207. doi: 10.1111/j.1471-4159.2012.07758.x. Epub 2012 May 9.

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