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Items: 1 to 20 of 103

1.

Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity.

Josifova DJ, Monroe GR, Tessadori F, de Graaff E, van der Zwaag B, Mehta SG; DDD Study, Harakalova M, Duran KJ, Savelberg SM, Nijman IJ, Jungbluth H, Hoogenraad CC, Bakkers J, Knoers NV, Firth HV, Beales PL, van Haaften G, van Haelst MM.

Hum Mol Genet. 2016 Jun 1;25(11):2158-2167. Epub 2016 Mar 22.

PMID:
27005418
2.

Novel Kidins220/ARMS Splice Isoforms: Potential Specific Regulators of Neuronal and Cardiovascular Development.

Schmieg N, Thomas C, Yabe A, Lynch DS, Iglesias T, Chakravarty P, Schiavo G.

PLoS One. 2015 Jun 17;10(6):e0129944. doi: 10.1371/journal.pone.0129944. eCollection 2015.

3.

Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures.

Mero IL, Mørk HH, Sheng Y, Blomhoff A, Opheim GL, Erichsen A, Vigeland MD, Selmer KK.

Hum Mol Genet. 2017 Oct 1;26(19):3792-3796. doi: 10.1093/hmg/ddx263.

PMID:
28934391
4.

Ankyrin repeat-rich membrane spanning/Kidins220 protein interacts with mammalian Septin 5.

Park HJ, Park HW, Lee SJ, Arevalo JC, Park YS, Lee SP, Paik KS, Chao MV, Chang MS.

Mol Cells. 2010 Aug;30(2):143-8. doi: 10.1007/s10059-010-0099-7. Epub 2010 Jul 23.

5.

Kidins220/ARMS regulates Rac1-dependent neurite outgrowth by direct interaction with the RhoGEF Trio.

Neubrand VE, Thomas C, Schmidt S, Debant A, Schiavo G.

J Cell Sci. 2010 Jun 15;123(Pt 12):2111-23. doi: 10.1242/jcs.064055.

6.

Kidins220/ARMS is transported by a kinesin-1-based mechanism likely to be involved in neuronal differentiation.

Bracale A, Cesca F, Neubrand VE, Newsome TP, Way M, Schiavo G.

Mol Biol Cell. 2007 Jan;18(1):142-52. Epub 2006 Nov 1.

7.

Kidins220/ARMS downregulation by excitotoxic activation of NMDARs reveals its involvement in neuronal survival and death pathways.

López-Menéndez C, Gascón S, Sobrado M, Vidaurre OG, Higuero AM, Rodríguez-Peña A, Iglesias T, Díaz-Guerra M.

J Cell Sci. 2009 Oct 1;122(Pt 19):3554-65. doi: 10.1242/jcs.056473.

8.

Kidins220/ARMS is dynamically expressed during Xenopus laevis development.

Marracci S, Giannini M, Vitiello M, Andreazzoli M, Dente L.

Int J Dev Biol. 2013;57(9-10):787-92. doi: 10.1387/ijdb.130080sm.

9.

Ankyrin Repeat-rich Membrane Spanning/Kidins220 protein regulates dendritic branching and spine stability in vivo.

Wu SH, Arévalo JC, Sarti F, Tessarollo L, Gan WB, Chao MV.

Dev Neurobiol. 2009 Aug;69(9):547-57. doi: 10.1002/dneu.20723.

10.

Kidins220/ARMS interacts with Pdzrn3, a protein containing multiple binding domains.

Andreazzoli M, Gestri G, Landi E, D'Orsi B, Barilari M, Iervolino A, Vitiello M, Wilson SW, Dente L.

Biochimie. 2012 Sep;94(9):2054-7. doi: 10.1016/j.biochi.2012.05.002. Epub 2012 May 15.

11.

Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity.

Parente DJ, Garriga C, Baskin B, Douglas G, Cho MT, Araujo GC, Shinawi M.

Am J Med Genet A. 2017 Jan;173(1):213-216. doi: 10.1002/ajmg.a.37977. Epub 2016 Nov 16.

PMID:
27865048
12.

Kidins220/ARMS as a functional mediator of multiple receptor signalling pathways.

Neubrand VE, Cesca F, Benfenati F, Schiavo G.

J Cell Sci. 2012 Apr 15;125(Pt 8):1845-54. doi: 10.1242/jcs.102764. Epub 2012 May 4.

13.

Developmental and activity-dependent regulation of ARMS/Kidins220 in cultured rat hippocampal neurons.

Cortés RY, Arévalo JC, Magby JP, Chao MV, Plummer MR.

Dev Neurobiol. 2007 Nov;67(13):1687-98.

14.

Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment.

Liu YF, Sowell SM, Luo Y, Chaubey A, Cameron RS, Kim HG, Srivastava AK.

PLoS One. 2015 Apr 22;10(4):e0123106. doi: 10.1371/journal.pone.0123106. eCollection 2015.

15.

Kidins220/ARMS modulates the activity of microtubule-regulating proteins and controls neuronal polarity and development.

Higuero AM, Sánchez-Ruiloba L, Doglio LE, Portillo F, Abad-Rodríguez J, Dotti CG, Iglesias T.

J Biol Chem. 2010 Jan 8;285(2):1343-57. doi: 10.1074/jbc.M109.024703. Epub 2009 Nov 10.

16.

Development of a neuroprotective peptide that preserves survival pathways by preventing Kidins220/ARMS calpain processing induced by excitotoxicity.

Gamir-Morralla A, López-Menéndez C, Ayuso-Dolado S, Tejeda GS, Montaner J, Rosell A, Iglesias T, Díaz-Guerra M.

Cell Death Dis. 2015 Oct 22;6:e1939. doi: 10.1038/cddis.2015.307.

17.

Ankyrin repeat-rich membrane spanning protein (kidins220) is required for neurotrophin and ephrin receptor-dependent dendrite development.

Chen Y, Fu WY, Ip JP, Ye T, Fu AK, Chao MV, Ip NY.

J Neurosci. 2012 Jun 13;32(24):8263-9. doi: 10.1523/JNEUROSCI.1264-12.2012.

18.

Differential regulation of kidins220 isoforms in Huntington's disease.

Sebastián-Serrano Á, Simón-García A, Belmonte-Alfaro A, Pose-Utrilla J, Santos-Galindo M, Del Puerto A, García-Guerra L, Hernández IH, Schiavo G, Campanero MR, Lucas JJ, Iglesias T.

Brain Pathol. 2019 Jul 2. doi: 10.1111/bpa.12761. [Epub ahead of print]

PMID:
31264746
19.

Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalance.

López-Menéndez C, Gamir-Morralla A, Jurado-Arjona J, Higuero AM, Campanero MR, Ferrer I, Hernández F, Ávila J, Díaz-Guerra M, Iglesias T.

Hum Mol Genet. 2013 Feb 1;22(3):466-82. doi: 10.1093/hmg/dds446. Epub 2012 Oct 31.

PMID:
23118350
20.

Identification of a novel FRMD7 splice variant and functional analysis of two FRMD7 transcripts during human NT2 cell differentiation.

Li Y, Pu J, Liu Z, Xu S, Jin F, Zhu L, Tian J, Luo J, Zhang B.

Mol Vis. 2011;17:2986-96. Epub 2011 Nov 17.

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