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See also: KIF1A kinesin family member 1A in the Gene database

kif1a in Homo sapiensMus musculusRattus norvegicusAll 223 Gene records

Search results

Items: 1 to 20 of 217

1.

Kinesin-3 Responds to Local Microtubule Dynamics to Target Synaptic Cargo Delivery to the Presynapse.

Guedes-Dias P, Nirschl JJ, Abreu N, Tokito MK, Janke C, Magiera MM, Holzbaur ELF.

Curr Biol. 2018 Dec 28. pii: S0960-9822(18)31595-1. doi: 10.1016/j.cub.2018.11.065. [Epub ahead of print]

PMID:
30612907
2.

The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case.

Yoshikawa K, Kuwahara M, Saigoh K, Ishiura H, Yamagishi Y, Hamano Y, Samukawa M, Suzuki H, Hirano M, Mitsui Y, Tsuji S, Kusunoki S.

eNeurologicalSci. 2018 Nov 22;14:34-37. doi: 10.1016/j.ensci.2018.11.026. eCollection 2019 Mar.

3.

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.

Coe BP, Stessman HAF, Sulovari A, Geisheker MR, Bakken TE, Lake AM, Dougherty JD, Lein ES, Hormozdiari F, Bernier RA, Eichler EE.

Nat Genet. 2019 Jan;51(1):106-116. doi: 10.1038/s41588-018-0288-4. Epub 2018 Dec 17.

PMID:
30559488
4.

Stromalin Constrains Memory Acquisition by Developmentally Limiting Synaptic Vesicle Pool Size.

Phan A, Thomas CI, Chakraborty M, Berry JA, Kamasawa N, Davis RL.

Neuron. 2019 Jan 2;101(1):103-118.e5. doi: 10.1016/j.neuron.2018.11.003. Epub 2018 Nov 28.

PMID:
30503644
5.

Sentryn Acts with a Subset of Active Zone Proteins To Optimize the Localization of Synaptic Vesicles in Caenorhabditis elegans.

Edwards SL, Morrison LM, Manning L, Stec N, Richmond JE, Miller KG.

Genetics. 2018 Nov;210(3):947-968. doi: 10.1534/genetics.118.301466.

6.

PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complex.

Samanta D, Gokden M.

J Clin Neurosci. 2018 Oct 29. pii: S0967-5868(18)31598-4. doi: 10.1016/j.jocn.2018.10.091. [Epub ahead of print]

PMID:
30385166
7.

Insights on UNC-104-dynein/dynactin interactions and their implications on axonal transport in Caenorhabditis elegans.

Chen CW, Peng YF, Yen YC, Bhan P, Muthaiyan Shanmugam M, Klopfenstein DR, Wagner OI.

J Neurosci Res. 2019 Feb;97(2):185-201. doi: 10.1002/jnr.24339. Epub 2018 Oct 12.

PMID:
30311677
8.

Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders.

Kashimada A, Hasegawa S, Nomura T, Shiraku H, Moriyama K, Suzuki T, Nakajima K, Mizuno T, Imai K, Sugawara Y, Morio T, Kumada S, Takagi M.

Brain Dev. 2018 Oct 6. pii: S0387-7604(18)30244-4. doi: 10.1016/j.braindev.2018.09.007. [Epub ahead of print]

PMID:
30301590
9.

Mechanochemical Model of the Power Stroke of the Single-Headed Motor Protein KIF1A.

Liu F, Ji Q, Wang H, Wang J.

J Phys Chem B. 2018 Sep 14. doi: 10.1021/acs.jpcb.8b04433. [Epub ahead of print]

PMID:
30179486
10.

Kinesin-1 Proteins KIF5A, -5B, and -5C Promote Anterograde Transport of Herpes Simplex Virus Enveloped Virions in Axons.

DuRaine G, Wisner TW, Howard P, Johnson DC.

J Virol. 2018 Sep 26;92(20). pii: e01269-18. doi: 10.1128/JVI.01269-18. Print 2018 Oct 15.

PMID:
30068641
11.

Regulation of KIF1A-Driven Dense Core Vesicle Transport: Ca2+/CaM Controls DCV Binding and Liprin-α/TANC2 Recruits DCVs to Postsynaptic Sites.

Stucchi R, Plucińska G, Hummel JJA, Zahavi EE, Guerra San Juan I, Klykov O, Scheltema RA, Altelaar AFM, Hoogenraad CC.

Cell Rep. 2018 Jul 17;24(3):685-700. doi: 10.1016/j.celrep.2018.06.071.

12.

Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients.

Lu C, Li LX, Dong HL, Wei Q, Liu ZJ, Ni W, Gitler AD, Wu ZY.

J Mol Med (Berl). 2018 Jul;96(7):701-712. doi: 10.1007/s00109-018-1655-4. Epub 2018 Jun 11.

PMID:
29934652
13.

The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes.

Travaglini L, Aiello C, Stregapede F, D'Amico A, Alesi V, Ciolfi A, Bruselles A, Catteruccia M, Pizzi S, Zanni G, Loddo S, Barresi S, Vasco G, Tartaglia M, Bertini E, Nicita F.

Neurogenetics. 2018 May;19(2):111-121. doi: 10.1007/s10048-018-0545-9. Epub 2018 Apr 24.

PMID:
29691679
14.

Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?

Demily C, Lesca G, Poisson A, Till M, Barcia G, Chatron N, Sanlaville D, Munnich A.

J Autism Dev Disord. 2018 Aug;48(8):2886-2889. doi: 10.1007/s10803-018-3552-7.

PMID:
29589274
15.

Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy.

Sferra A, Fattori F, Rizza T, Flex E, Bellacchio E, Bruselles A, Petrini S, Cecchetti S, Teson M, Restaldi F, Ciolfi A, Santorelli FM, Zanni G, Barresi S, Castiglioni C, Tartaglia M, Bertini E.

Hum Mol Genet. 2018 Jun 1;27(11):1892-1904. doi: 10.1093/hmg/ddy096.

PMID:
29547997
16.

The C-terminal of CASY-1/Calsyntenin regulates GABAergic synaptic transmission at the Caenorhabditis elegans neuromuscular junction.

Thapliyal S, Vasudevan A, Dong Y, Bai J, Koushika SP, Babu K.

PLoS Genet. 2018 Mar 12;14(3):e1007263. doi: 10.1371/journal.pgen.1007263. eCollection 2018 Mar.

17.

Neuroprotection Exerted by Netrin-1 and Kinesin Motor KIF1A in Secondary Brain Injury following Experimental Intracerebral Hemorrhage in Rats.

Wang J, Zhai W, Yu Z, Sun L, Li H, Shen H, Li X, Liu C, Chen G.

Front Cell Neurosci. 2018 Jan 11;11:432. doi: 10.3389/fncel.2017.00432. eCollection 2017.

18.

Axonal transport in a peripheral diabetic neuropathy model: sex-dimorphic features.

Pesaresi M, Giatti S, Spezzano R, Romano S, Diviccaro S, Borsello T, Mitro N, Caruso D, Garcia-Segura LM, Melcangi RC.

Biol Sex Differ. 2018 Jan 19;9(1):6. doi: 10.1186/s13293-018-0164-z.

19.

Capture of Dense Core Vesicles at Synapses by JNK-Dependent Phosphorylation of Synaptotagmin-4.

Bharat V, Siebrecht M, Burk K, Ahmed S, Reissner C, Kohansal-Nodehi M, Steubler V, Zweckstetter M, Ting JT, Dean C.

Cell Rep. 2017 Nov 21;21(8):2118-2133. doi: 10.1016/j.celrep.2017.10.084.

20.

Multigeneration family with dominant SPG30 hereditary spastic paraplegia.

Roda RH, Schindler AB, Blackstone C.

Ann Clin Transl Neurol. 2017 Oct 14;4(11):821-824. doi: 10.1002/acn3.452. eCollection 2017 Nov.

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