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Results: 1 to 20 of 119

1.

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.

Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N.

Cell. 2001 Jun 1;105(5):587-97. Erratum in: Cell 2001 Jul 13;106(1):127.

PMID:
11389829
[PubMed - indexed for MEDLINE]
Free Article
2.

A novel kinesin-like protein, KIF1Bbeta3 is involved in the movement of lysosomes to the cell periphery in non-neuronal cells.

Matsushita M, Tanaka S, Nakamura N, Inoue H, Kanazawa H.

Traffic. 2004 Mar;5(3):140-51.

PMID:
15086790
[PubMed - indexed for MEDLINE]
3.

Genomic structure and mutational analysis of the human KIF1Balpha gene located at 1p36.2 in neuroblastoma.

Chen YY, Takita J, Chen YZ, Yang HW, Hanada R, Yamamoto K, Hayashi Y.

Int J Oncol. 2003 Sep;23(3):737-44.

PMID:
12888911
[PubMed - indexed for MEDLINE]
4.

The major brain isoform of kif1b lacks the putative mitochondria-binding domain.

Conforti L, Buckmaster EA, Tarlton A, Brown MC, Lyon MF, Perry VH, Coleman MP.

Mamm Genome. 1999 Jun;10(6):617-22.

PMID:
10341097
[PubMed - indexed for MEDLINE]
5.

Kif1Bbeta isoform is enriched in motor neurons but does not change in a mouse model of amyotrophic lateral sclerosis.

Conforti L, Dell'Agnello C, Calvaresi N, Tortarolo M, Giorgini A, Coleman MP, Bendotti C.

J Neurosci Res. 2003 Mar 1;71(5):732-9.

PMID:
12584731
[PubMed - indexed for MEDLINE]
6.

Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene.

Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E.

Neurology. 2004 May 11;62(9):1522-5.

PMID:
15136675
[PubMed - indexed for MEDLINE]
7.

The kinesin superfamily protein Rab6KIFL is not involved in the pathophysiology of Charcot-Marie-Tooth disease type 4C.

Nagura M, Nagao Y, Takita J, Igarashi T, LeGuern E, Hayashi Y.

Int J Mol Med. 2003 Jan;11(1):45-7.

PMID:
12469216
[PubMed - indexed for MEDLINE]
8.

KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria.

Nangaku M, Sato-Yoshitake R, Okada Y, Noda Y, Takemura R, Yamazaki H, Hirokawa N.

Cell. 1994 Dec 30;79(7):1209-20.

PMID:
7528108
[PubMed - indexed for MEDLINE]
9.

Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport.

Pérez-Ollé R, López-Toledano MA, Goryunov D, Cabrera-Poch N, Stefanis L, Brown K, Liem RK.

J Neurochem. 2005 May;93(4):861-74.

PMID:
15857389
[PubMed - indexed for MEDLINE]
10.

Altered motor activity of alternative splice variants of the mammalian kinesin-3 protein KIF1B.

Matsushita M, Yamamoto R, Mitsui K, Kanazawa H.

Traffic. 2009 Nov;10(11):1647-54. doi: 10.1111/j.1600-0854.2009.00975.x. Epub 2009 Aug 10.

PMID:
19744141
[PubMed - indexed for MEDLINE]
12.

Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.

Cartoni R, Arnaud E, Médard JJ, Poirot O, Courvoisier DS, Chrast R, Martinou JC.

Brain. 2010 May;133(Pt 5):1460-9. doi: 10.1093/brain/awq082.

PMID:
20418531
[PubMed - indexed for MEDLINE]
Free Article
13.

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N.

Am J Hum Genet. 2002 Mar;70(3):726-36. Epub 2002 Jan 17. Erratum in: Am J Hum Genet 2002 Apr;70(4):1075.

PMID:
11799477
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Defect in synaptic vesicle precursor transport and neuronal cell death in KIF1A motor protein-deficient mice.

Yonekawa Y, Harada A, Okada Y, Funakoshi T, Kanai Y, Takei Y, Terada S, Noda T, Hirokawa N.

J Cell Biol. 1998 Apr 20;141(2):431-41.

PMID:
9548721
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2.

Yang HW, Chen YZ, Takita J, Soeda E, Piao HY, Hayashi Y.

Oncogene. 2001 Aug 16;20(36):5075-83.

PMID:
11526494
[PubMed - indexed for MEDLINE]
Free Article
16.

KIF1Bbeta2, capable of interacting with CHP, is localized to synaptic vesicles.

Nakamura N, Miyake Y, Matsushita M, Tanaka S, Inoue H, Kanazawa H.

J Biochem. 2002 Sep;132(3):483-91.

PMID:
12204119
[PubMed - indexed for MEDLINE]
Free Article
17.

KIF1Bβ transports dendritically localized mRNPs in neurons and is recruited to synapses in an activity-dependent manner.

Charalambous DC, Pasciuto E, Mercaldo V, Pilo Boyl P, Munck S, Bagni C, Santama N.

Cell Mol Life Sci. 2013 Jan;70(2):335-56. doi: 10.1007/s00018-012-1108-0. Epub 2012 Sep 4.

PMID:
22945799
[PubMed - indexed for MEDLINE]
18.

Molecular motors: from one motor many tails to one motor many tales.

Goldstein LS.

Trends Cell Biol. 2001 Dec;11(12):477-82. Review.

PMID:
11719052
[PubMed - indexed for MEDLINE]
19.

Loss of alpha-tubulin polyglutamylation in ROSA22 mice is associated with abnormal targeting of KIF1A and modulated synaptic function.

Ikegami K, Heier RL, Taruishi M, Takagi H, Mukai M, Shimma S, Taira S, Hatanaka K, Morone N, Yao I, Campbell PK, Yuasa S, Janke C, Macgregor GR, Setou M.

Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3213-8. Epub 2007 Feb 20.

PMID:
17360631
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Novel dendritic kinesin sorting identified by different process targeting of two related kinesins: KIF21A and KIF21B.

Marszalek JR, Weiner JA, Farlow SJ, Chun J, Goldstein LS.

J Cell Biol. 1999 May 3;145(3):469-79.

PMID:
10225949
[PubMed - indexed for MEDLINE]
Free PMC Article

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