Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 178

1.

Interaction between LIS1 and doublecortin, two lissencephaly gene products.

Caspi M, Atlas R, Kantor A, Sapir T, Reiner O.

Hum Mol Genet. 2000 Sep 22;9(15):2205-13.

2.

Doublecortin, a stabilizer of microtubules.

Horesh D, Sapir T, Francis F, Wolf SG, Caspi M, Elbaum M, Chelly J, Reiner O.

Hum Mol Genet. 1999 Sep;8(9):1599-610.

3.

A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function.

Faulkner NE, Dujardin DL, Tai CY, Vaughan KT, O'Connell CB, Wang Y, Vallee RB.

Nat Cell Biol. 2000 Nov;2(11):784-91.

PMID:
11056532
4.

Colocalization of doublecortin with the microtubules: an ex vivo colocalization study of mutant doublecortin.

Yoshiura K, Noda Y, Kinoshita A, Niikawa N.

J Neurobiol. 2000 May;43(2):132-9.

PMID:
10770842
5.
6.

NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins.

Sweeney KJ, Prokscha A, Eichele G.

Mech Dev. 2001 Mar;101(1-2):21-33.

7.

Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes.

Friocourt G, Kappeler C, Saillour Y, Fauchereau F, Rodriguez MS, Bahi N, Vinet MC, Chafey P, Poirier K, Taya S, Wood SA, Dargemont C, Francis F, Chelly J.

Mol Cell Neurosci. 2005 Jan;28(1):153-64.

PMID:
15607950
8.

Neurabin II mediates doublecortin-dephosphorylation on actin filaments.

Tsukada M, Prokscha A, Eichele G.

Biochem Biophys Res Commun. 2006 May 12;343(3):839-47. Epub 2006 Mar 20.

PMID:
16564023
9.

Doublecortin mutations cluster in evolutionarily conserved functional domains.

Sapir T, Horesh D, Caspi M, Atlas R, Burgess HA, Wolf SG, Francis F, Chelly J, Elbaum M, Pietrokovski S, Reiner O.

Hum Mol Genet. 2000 Mar 22;9(5):703-12. Erratum in: Hum Mol Genet 2000 May 22;9(9):1461.

10.

Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration.

Tanaka T, Serneo FF, Higgins C, Gambello MJ, Wynshaw-Boris A, Gleeson JG.

J Cell Biol. 2004 Jun 7;165(5):709-21. Epub 2004 Jun 1.

11.

Doublecortin association with actin filaments is regulated by neurabin II.

Tsukada M, Prokscha A, Ungewickell E, Eichele G.

J Biol Chem. 2005 Mar 25;280(12):11361-8. Epub 2005 Jan 4.

12.

Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different.

Viot G, Sonigo P, Simon I, Simon-Bouy B, Chadeyron F, Beldjord C, Tantau J, Martinovic J, Esculpavit C, Brunelle F, Munnich A, Vekemans M, Encha-Razavi F.

Am J Med Genet A. 2004 Apr 15;126A(2):123-8.

PMID:
15057976
13.

Lis1 and Ndel1 influence the timing of nuclear envelope breakdown in neural stem cells.

Hebbar S, Mesngon MT, Guillotte AM, Desai B, Ayala R, Smith DS.

J Cell Biol. 2008 Sep 22;182(6):1063-71. doi: 10.1083/jcb.200803071.

14.

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.

Pilz DT, Kuc J, Matsumoto N, Bodurtha J, Bernadi B, Tassinari CA, Dobyns WB, Ledbetter DH.

Hum Mol Genet. 1999 Sep;8(9):1757-60.

15.

Missense mutations resulting in type 1 lissencephaly.

Reiner O, Coquelle FM.

Cell Mol Life Sci. 2005 Feb;62(4):425-34. Review.

PMID:
15719169
16.

Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.

Couillard-Despres S, Uyanik G, Ploetz S, Karl C, Koch H, Winkler J, Aigner L.

Neurogenetics. 2004 Jun;5(2):83-93. Epub 2004 Mar 25.

PMID:
15045646
17.
18.

Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization.

Cahana A, Escamez T, Nowakowski RS, Hayes NL, Giacobini M, von Holst A, Shmueli O, Sapir T, McConnell SK, Wurst W, Martinez S, Reiner O.

Proc Natl Acad Sci U S A. 2001 May 22;98(11):6429-34. Epub 2001 May 8.

19.

Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects.

Pramparo T, Libiger O, Jain S, Li H, Youn YH, Hirotsune S, Schork NJ, Wynshaw-Boris A.

PLoS Genet. 2011 Mar;7(3):e1001331. doi: 10.1371/journal.pgen.1001331. Epub 2011 Mar 10.

20.

Location and type of mutation in the LIS1 gene do not predict phenotypic severity.

Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Ad├Ęs L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J.

Neurology. 2007 Jul 31;69(5):442-7.

PMID:
17664403
Items per page

Supplemental Content

Write to the Help Desk