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Results: 1 to 20 of 106

Similar articles for PubMed (Select 24446295)

1.

No association between FGD1 gene polymorphisms and intellectual developmental disability in the Qinba mountain area.

Li JL, Li YJ, Zhang KJ, Lan L, Shi JG, Yang X, Zhang MJ, Zhang FC, Gao XC.

Genet Mol Res. 2014 Jan 10;13(1):127-33. doi: 10.4238/2014.January.10.3.

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FGD1 as a central regulator of extracellular matrix remodelling--lessons from faciogenital dysplasia.

Genot E, Daubon T, Sorrentino V, Buccione R.

J Cell Sci. 2012 Jul 15;125(Pt 14):3265-70. doi: 10.1242/jcs.093419. Epub 2012 Aug 1.

4.

The Cdc42 guanine nucleotide exchange factor FGD1 regulates osteogenesis in human mesenchymal stem cells.

Gao L, Gorski JL, Chen CS.

Am J Pathol. 2011 Mar;178(3):969-74. doi: 10.1016/j.ajpath.2010.11.051.

7.

The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor.

Zheng Y, Fischer DJ, Santos MF, Tigyi G, Pasteris NG, Gorski JL, Xu Y.

J Biol Chem. 1996 Dec 27;271(52):33169-72.

8.

MLK3 regulates bone development downstream of the faciogenital dysplasia protein FGD1 in mice.

Zou W, Greenblatt MB, Shim JH, Kant S, Zhai B, Lotinun S, Brady N, Hu DZ, Gygi SP, Baron R, Davis RJ, Jones D, Glimcher LH.

J Clin Invest. 2011 Nov;121(11):4383-92. doi: 10.1172/JCI59041. Epub 2011 Oct 3.

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10.

Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.

Pasteris NG, Buckler J, Cadle AB, Gorski JL.

Genomics. 1997 Aug 1;43(3):390-4.

PMID:
9268645
11.

A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome).

Orrico A, Galli L, Falciani M, Bracci M, Cavaliere ML, Rinaldi MM, Musacchio A, Sorrentino V.

FEBS Lett. 2000 Aug 4;478(3):216-20.

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Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients.

Orrico A, Galli L, Cavaliere ML, Garavelli L, Fryns JP, Crushell E, Rinaldi MM, Medeira A, Sorrentino V.

Eur J Hum Genet. 2004 Jan;12(1):16-23.

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18.

Faciogenital dysplasia protein (FGD1) regulates export of cargo proteins from the golgi complex via Cdc42 activation.

Egorov MV, Capestrano M, Vorontsova OA, Di Pentima A, Egorova AV, Mariggiò S, Ayala MI, Tetè S, Gorski JL, Luini A, Buccione R, Polishchuk RS.

Mol Biol Cell. 2009 May;20(9):2413-27. doi: 10.1091/mbc.E08-11-1136. Epub 2009 Mar 4.

20.

First case of deletion of the faciogenital dysplasia 1 (FGD1) gene in a patient with Aarskog-Scott syndrome.

Bedoyan JK, Friez MJ, DuPont B, Ahmad A.

Eur J Med Genet. 2009 Jul-Aug;52(4):262-4. doi: 10.1016/j.ejmg.2008.12.001. Epub 2008 Dec 16.

PMID:
19110080
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