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Results: 1 to 20 of 321

PubMed for Gene (Select 2316)

1.

A mechanism of global shape-dependent recognition and phosphorylation of filamin by protein kinase A.

Ithychanda SS, Fang X, Mohan ML, Zhu L, Tirupula KC, Naga Prasad SV, Wang YX, Karnik SS, Qin J.

J Biol Chem. 2015 Mar 27;290(13):8527-38. doi: 10.1074/jbc.M114.633446. Epub 2015 Feb 9.

PMID:
25666618
2.

Phosphorylation of filamin A by Cdk1 regulates filamin A localization and daughter cell separation.

Szeto SG, Williams EC, Rudner AD, Lee JM.

Exp Cell Res. 2015 Jan 15;330(2):248-66. doi: 10.1016/j.yexcr.2014.10.024. Epub 2014 Nov 13.

PMID:
25445790
3.

[Filamin A as a mediator of alterations in cancer cells].

Wieczorek K, Niewiarowska J.

Postepy Biochem. 2014;60(1):77-83. Review. Polish.

PMID:
25033545
4.

Filamin A expression correlates with proliferation and invasive properties of human metastatic melanoma tumors: implications for survival in patients.

Zhang K, Zhu T, Gao D, Zhang Y, Zhao Q, Liu S, Su T, Bernier M, Zhao R.

J Cancer Res Clin Oncol. 2014 Nov;140(11):1913-26. doi: 10.1007/s00432-014-1722-3. Epub 2014 Jun 8.

PMID:
24908328
5.

Interactions between filamin A and MMP-9 regulate proliferation and invasion in renal cell carcinoma.

Sun GG, Wei CD, Jing SW, Hu WN.

Asian Pac J Cancer Prev. 2014;15(8):3789-95.

6.

Force-dependent isomerization kinetics of a highly conserved proline switch modulates the mechanosensing region of filamin.

Rognoni L, Möst T, Žoldák G, Rief M.

Proc Natl Acad Sci U S A. 2014 Apr 15;111(15):5568-73. doi: 10.1073/pnas.1319448111. Epub 2014 Apr 2.

7.

An antiproliferative gene FLNA regulates migration and invasion of gastric carcinoma cell in vitro and its clinical significance.

Sun GG, Sheng SH, Jing SW, Hu WN.

Tumour Biol. 2014 Mar;35(3):2641-8. doi: 10.1007/s13277-013-1347-1. Epub 2013 Nov 16.

PMID:
24241900
8.

Absent expression of FLNA is correlated with poor prognosis of nasopharyngeal cancer.

Sun GG, Lu YF, Cheng YJ, Hu WN.

Tumour Biol. 2014 Apr;35(4):2967-74. doi: 10.1007/s13277-013-1381-z. Epub 2013 Nov 12.

PMID:
24218340
9.

Novel no-stop FLNA mutation causes multi-organ involvement in males.

Oegema R, Hulst JM, Theuns-Valks SD, van Unen LM, Schot R, Mancini GM, Schipper ME, de Wit MC, Sibbles BJ, de Coo IF, Nanninga V, Hofstra RM, Halley DJ, Brooks AS.

Am J Med Genet A. 2013 Sep;161A(9):2376-84. doi: 10.1002/ajmg.a.36109. Epub 2013 Jul 19.

PMID:
23873601
10.

Heterogeneity of platelet functional alterations in patients with filamin A mutations.

Berrou E, Adam F, Lebret M, Fergelot P, Kauskot A, Coupry I, Jandrot-Perrus M, Nurden A, Favier R, Rosa JP, Goizet C, Nurden P, Bryckaert M.

Arterioscler Thromb Vasc Biol. 2013 Jan;33(1):e11-8. doi: 10.1161/ATVBAHA.112.300603. Epub 2012 Nov 1.

11.

Electron microscopy and 3D reconstruction reveals filamin Ig domain binding to F-actin.

Suphamungmee W, Nakamura F, Hartwig JH, Lehman W.

J Mol Biol. 2012 Dec 14;424(5):248-56. doi: 10.1016/j.jmb.2012.09.025. Epub 2012 Oct 4.

12.

Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutations.

van der Werf CS, Sribudiani Y, Verheij JB, Carroll M, O'Loughlin E, Chen CH, Brooks AS, Liszewski MK, Atkinson JP, Hofstra RM.

Genet Med. 2013 Apr;15(4):310-3. doi: 10.1038/gim.2012.123. Epub 2012 Oct 4.

PMID:
23037936
13.

Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.

Reinstein E, Frentz S, Morgan T, García-Miñaúr S, Leventer RJ, McGillivray G, Pariani M, van der Steen A, Pope M, Holder-Espinasse M, Scott R, Thompson EM, Robertson T, Coppin B, Siegel R, Bret Zurita M, Rodríguez JI, Morales C, Rodrigues Y, Arcas J, Saggar A, Horton M, Zackai E, Graham JM, Rimoin DL, Robertson SP.

Eur J Hum Genet. 2013 May;21(5):494-502. doi: 10.1038/ejhg.2012.209. Epub 2012 Oct 3.

14.

Filamin A-hinge region 1-EGFP: a novel tool for tracking the cellular functions of filamin A in real-time.

Planagumà J, Minsaas L, Pons M, Myhren L, Garrido G, Aragay AM.

PLoS One. 2012;7(8):e40864. doi: 10.1371/journal.pone.0040864. Epub 2012 Aug 1.

15.

Filamin A mutation associated with normal reading skills and dyslexia in a family with periventricular heterotopia.

Reinstein E, Chang BS, Robertson SP, Rimoin DL, Katzir T.

Am J Med Genet A. 2012 Aug;158A(8):1897-901. doi: 10.1002/ajmg.a.35455. Epub 2012 Jun 27.

PMID:
22740120
16.

The C-terminal rod 2 fragment of filamin A forms a compact structure that can be extended.

Ruskamo S, Gilbert R, Hofmann G, Jiang P, Campbell ID, Ylänne J, Pentikäinen U.

Biochem J. 2012 Sep 1;446(2):261-9. doi: 10.1042/BJ20120361.

PMID:
22676060
17.

Atypical male and female presentations of FLNA-related periventricular nodular heterotopia.

Fergelot P, Coupry I, Rooryck C, Deforges J, Maurat E, Solé G, Boute O, Dieux-Coeslier A, David A, Marchal C, Thambo JB, Lacombe D, Arveiler B, Goizet C.

Eur J Med Genet. 2012 May;55(5):313-8. doi: 10.1016/j.ejmg.2012.01.018. Epub 2012 Feb 8.

PMID:
22366253
18.

Cytoskeletal protein filamin A is a nucleolar protein that suppresses ribosomal RNA gene transcription.

Deng W, Lopez-Camacho C, Tang JY, Mendoza-Villanueva D, Maya-Mendoza A, Jackson DA, Shore P.

Proc Natl Acad Sci U S A. 2012 Jan 31;109(5):1524-9. doi: 10.1073/pnas.1107879109. Epub 2012 Jan 17.

19.

FLNA genomic rearrangements cause periventricular nodular heterotopia.

Clapham KR, Yu TW, Ganesh VS, Barry B, Chan Y, Mei D, Parrini E, Funalot B, Dupuis L, Nezarati MM, du Souich C, van Karnebeek C, Guerrini R, Walsh CA.

Neurology. 2012 Jan 24;78(4):269-78. doi: 10.1212/WNL.0b013e31824365e4. Epub 2012 Jan 11.

20.

Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome.

Nurden P, Debili N, Coupry I, Bryckaert M, Youlyouz-Marfak I, Solé G, Pons AC, Berrou E, Adam F, Kauskot A, Lamazière JM, Rameau P, Fergelot P, Rooryck C, Cailley D, Arveiler B, Lacombe D, Vainchenker W, Nurden A, Goizet C.

Blood. 2011 Nov 24;118(22):5928-37. doi: 10.1182/blood-2011-07-365601. Epub 2011 Sep 29.

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