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

kif1a in Homo sapiensMus musculusRattus norvegicusAll 242 Gene records

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Items: 1 to 20 of 235

1.

Going Too Far Is the Same as Falling Short: Kinesin-3 Family Members in Hereditary Spastic Paraplegia.

Gabrych DR, Lau VZ, Niwa S, Silverman MA.

Front Cell Neurosci. 2019 Sep 26;13:419. doi: 10.3389/fncel.2019.00419. eCollection 2019. Review.

2.

Co-expression network analysis identified hub genes critical to triglyceride and free fatty acid metabolism as key regulators of age-related vascular dysfunction in mice.

Li H, Wang X, Lu X, Zhu H, Li S, Duan S, Zhao X, Zhang F, Alterovitz G, Wang F, Li Q, Tian XL, Xu M.

Aging (Albany NY). 2019 Sep 12;11(18):7620-7638. doi: 10.18632/aging.102275. Epub 2019 Sep 12.

3.

Rett and Rett-like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene.

Wang J, Zhang Q, Chen Y, Yu S, Wu X, Bao X.

Mol Genet Genomic Med. 2019 Sep 11:e968. doi: 10.1002/mgg3.968. [Epub ahead of print]

4.

Control of Intestinal Cell Fate by Dynamic Mitotic Spindle Repositioning Influences Epithelial Homeostasis and Longevity.

Hu DJ, Jasper H.

Cell Rep. 2019 Sep 10;28(11):2807-2823.e5. doi: 10.1016/j.celrep.2019.08.014.

5.

KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia.

Pennings M, Schouten MI, van Gaalen J, Meijer RPP, de Bot ST, Kriek M, Saris CGJ, van den Berg LH, van Es MA, Zuidgeest DMH, Elting MW, van de Kamp JM, van Spaendonck-Zwarts KY, Die-Smulders C, Brilstra EH, Verschuuren CC, de Vries BBA, Bruijn J, Sofou K, Duijkers FA, Jaeger B, Schieving JH, van de Warrenburg BP, Kamsteeg EJ.

Eur J Hum Genet. 2019 Sep 5. doi: 10.1038/s41431-019-0497-z. [Epub ahead of print]

PMID:
31488895
6.

A novel strategy to visualize vesicle-bound kinesins reveals the diversity of kinesin-mediated transport.

Yang R, Bostick Z, Garbouchian A, Luisi J, Banker G, Bentley M.

Traffic. 2019 Nov;20(11):851-866. doi: 10.1111/tra.12692. Epub 2019 Oct 2.

PMID:
31461551
7.

Disease-associated mutations hyperactivate KIF1A motility and anterograde axonal transport of synaptic vesicle precursors.

Chiba K, Takahashi H, Chen M, Obinata H, Arai S, Hashimoto K, Oda T, McKenney RJ, Niwa S.

Proc Natl Acad Sci U S A. 2019 Sep 10;116(37):18429-18434. doi: 10.1073/pnas.1905690116. Epub 2019 Aug 27.

PMID:
31455732
8.

Genetic parameters and genome-wide association study regarding feed efficiency and slaughter traits in Charolais cows.

Martin P, Taussat S, Vinet A, Krauss D, Maupetit D, Renand G.

J Anim Sci. 2019 Sep 3;97(9):3684-3698. doi: 10.1093/jas/skz240.

PMID:
31436836
9.

Genetic heterogeneity in infantile spasms.

Muir AM, Myers CT, Nguyen NT, Saykally J, Craiu D, De Jonghe P, Helbig I, Hoffman-Zacharska D, Guerrini R, Lehesjoki AE, Marini C, Møller RS, Serratosa J, Štěrbová K, Striano P, von Spiczak S, Weckhuysen S, Mefford HC; EuroEPINOMICS-RES NLES working group, Sarah Weckhuysen.

Epilepsy Res. 2019 Oct;156:106181. doi: 10.1016/j.eplepsyres.2019.106181. Epub 2019 Jul 29.

PMID:
31394400
10.

SerThr-PhosphoProteome of Brain from Aged PINK1-KO+A53T-SNCA Mice Reveals pT1928-MAP1B and pS3781-ANK2 Deficits, as Hub between Autophagy and Synapse Changes.

Auburger G, Gispert S, Torres-Odio S, Jendrach M, Brehm N, Canet-Pons J, Key J, Sen NE.

Int J Mol Sci. 2019 Jul 4;20(13). pii: E3284. doi: 10.3390/ijms20133284.

11.

Author Correction: Formation of helical membrane tubes around microtubules by single-headed kinesin KIF1A.

Oriola D, Roth S, Dogterom M, Casademunt J.

Nat Commun. 2019 Jul 2;10(1):2941. doi: 10.1038/s41467-019-11010-5.

12.

The Conserved IgSF9 Protein Borderless Regulates Axonal Transport of Presynaptic Components and Color Vision in Drosophila.

Shaw HS, Cameron SA, Chang WT, Rao Y.

J Neurosci. 2019 Aug 28;39(35):6817-6828. doi: 10.1523/JNEUROSCI.0075-19.2019. Epub 2019 Jun 24.

PMID:
31235647
13.

βII-spectrin promotes mouse brain connectivity through stabilizing axonal plasma membranes and enabling axonal organelle transport.

Lorenzo DN, Badea A, Zhou R, Mohler PJ, Zhuang X, Bennett V.

Proc Natl Acad Sci U S A. 2019 Jul 30;116(31):15686-15695. doi: 10.1073/pnas.1820649116. Epub 2019 Jun 17.

PMID:
31209033
14.

A Brownian Ratchet Model Explains the Biased Sidestepping of Single-Headed Kinesin-3 KIF1A.

Mitra A, Suñé M, Diez S, Sancho JM, Oriola D, Casademunt J.

Biophys J. 2019 Jun 18;116(12):2266-2274. doi: 10.1016/j.bpj.2019.05.011. Epub 2019 May 18.

PMID:
31155147
15.

Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: De novo mutation of the KIF1A gene, a new hope in prognosis.

Urtiaga Valle S, Fournier Gil B, Ramiro León MS, Martínez Menéndez B.

Neurologia. 2019 Mar 9. pii: S0213-4853(18)30197-X. doi: 10.1016/j.nrl.2018.07.001. [Epub ahead of print] English, Spanish. No abstract available.

16.

Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.

Elert-Dobkowska E, Stepniak I, Krysa W, Ziora-Jakutowicz K, Rakowicz M, Sobanska A, Pilch J, Antczak-Marach D, Zaremba J, Sulek A.

Neurogenetics. 2019 Mar;20(1):27-38. doi: 10.1007/s10048-019-00565-6. Epub 2019 Feb 19.

17.

Polyglutamylation of tubulin's C-terminal tail controls pausing and motility of kinesin-3 family member KIF1A.

Lessard DV, Zinder OJ, Hotta T, Verhey KJ, Ohi R, Berger CL.

J Biol Chem. 2019 Apr 19;294(16):6353-6363. doi: 10.1074/jbc.RA118.005765. Epub 2019 Feb 15.

PMID:
30770469
18.

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. 2019 Jan 21;29(2):268-282.e8. doi: 10.1016/j.cub.2018.11.065. Epub 2019 Jan 3.

PMID:
30612907
19.

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.

20.

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.

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