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Results: 1 to 20 of 105

Similar articles for PubMed (Select 12185600)

2.

Genomic organization and expression profile of the human and mouse WAVE gene family.

Sossey-Alaoui K, Head K, Nowak N, Cowell JK.

Mamm Genome. 2003 May;14(5):314-22.

PMID:
12856283
5.

Identification of two human WAVE/SCAR homologues as general actin regulatory molecules which associate with the Arp2/3 complex.

Suetsugu S, Miki H, Takenawa T.

Biochem Biophys Res Commun. 1999 Jun 24;260(1):296-302.

PMID:
10381382
6.
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10.

Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.

Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N.

Eur J Cancer. 1995;31A(4):523-6.

PMID:
7576958
11.

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.

12.

WAVE3 promotes cell motility and invasion through the regulation of MMP-1, MMP-3, and MMP-9 expression.

Sossey-Alaoui K, Ranalli TA, Li X, Bakin AV, Cowell JK.

Exp Cell Res. 2005 Aug 1;308(1):135-45. Erratum in: Exp Cell Res. 2013 Mar 10;319(5):775. Exp Cell Res. 2010 Oct 15;316(17):3006.

PMID:
15907837
13.

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
14.

Genome analysis and gene expression profiling of neuroblastoma and ganglioneuroblastoma reveal differences between neuroblastic and Schwannian stromal cells.

Coco S, Defferrari R, Scaruffi P, Cavazzana A, Di Cristofano C, Longo L, Mazzocco K, Perri P, Gambini C, Moretti S, Bonassi S, Tonini GP.

J Pathol. 2005 Nov;207(3):346-57.

PMID:
16178058
16.

WAVE3 functions as a negative regulator of LDOC1.

Mizutani K, Koike D, Suetsugu S, Takenawa T.

J Biochem. 2005 Nov;138(5):639-46.

PMID:
16272576
17.

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint.

Tentler D, Brandberg G, Betancur C, Gillberg C, Annerén G, Orsmark C, Green ED, Carlsson B, Dahl N.

Am J Med Genet. 2001 Dec 8;105(8):729-36.

PMID:
11803521
19.

WAVE3-mediated cell migration and lamellipodia formation are regulated downstream of phosphatidylinositol 3-kinase.

Sossey-Alaoui K, Li X, Ranalli TA, Cowell JK.

J Biol Chem. 2005 Jun 10;280(23):21748-55. Epub 2005 Apr 11.

20.

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.

Hearn T, Renforth GL, Spalluto C, Hanley NA, Piper K, Brickwood S, White C, Connolly V, Taylor JF, Russell-Eggitt I, Bonneau D, Walker M, Wilson DI.

Nat Genet. 2002 May;31(1):79-83. Epub 2002 Apr 8.

PMID:
11941370
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