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Similar articles for PubMed (Select 17925330)

1.

LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability.

Dimmer KS, Navoni F, Casarin A, Trevisson E, Endele S, Winterpacht A, Salviati L, Scorrano L.

Hum Mol Genet. 2008 Jan 15;17(2):201-14. Epub 2007 Oct 9.

2.

LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition.

Hart L, Rauch A, Carr AM, Vermeesch JR, O'Driscoll M.

Dis Model Mech. 2014 May;7(5):535-45. doi: 10.1242/dmm.014464. Epub 2014 Mar 13.

3.

LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein.

Schlickum S, Moghekar A, Simpson JC, Steglich C, O'Brien RJ, Winterpacht A, Endele SU.

Genomics. 2004 Feb;83(2):254-61.

PMID:
14706454
4.

A Drosophila mutant of LETM1, a candidate gene for seizures in Wolf-Hirschhorn syndrome.

McQuibban AG, Joza N, Megighian A, Scorzeto M, Zanini D, Reipert S, Richter C, Schweyen RJ, Nowikovsky K.

Hum Mol Genet. 2010 Mar 15;19(6):987-1000. doi: 10.1093/hmg/ddp563. Epub 2009 Dec 21.

5.
6.

Characterization of the mitochondrial protein LETM1, which maintains the mitochondrial tubular shapes and interacts with the AAA-ATPase BCS1L.

Tamai S, Iida H, Yokota S, Sayano T, Kiguchiya S, Ishihara N, Hayashi J, Mihara K, Oka T.

J Cell Sci. 2008 Aug 1;121(Pt 15):2588-600. doi: 10.1242/jcs.026625. Epub 2008 Jul 15.

7.

Letm1, the mitochondrial Ca2+/H+ antiporter, is essential for normal glucose metabolism and alters brain function in Wolf-Hirschhorn syndrome.

Jiang D, Zhao L, Clish CB, Clapham DE.

Proc Natl Acad Sci U S A. 2013 Jun 11;110(24):E2249-54. doi: 10.1073/pnas.1308558110. Epub 2013 May 28.

8.

Association of LETM1 and MRPL36 contributes to the regulation of mitochondrial ATP production and necrotic cell death.

Piao L, Li Y, Kim SJ, Byun HS, Huang SM, Hwang SK, Yang KJ, Park KA, Won M, Hong J, Hur GM, Seok JH, Shong M, Cho MH, Brazil DP, Hemmings BA, Park J.

Cancer Res. 2009 Apr 15;69(8):3397-404. doi: 10.1158/0008-5472.CAN-08-3235. Epub 2009 Mar 24.

9.

The LETM1/YOL027 gene family encodes a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome.

Nowikovsky K, Froschauer EM, Zsurka G, Samaj J, Reipert S, Kolisek M, Wiesenberger G, Schweyen RJ.

J Biol Chem. 2004 Jul 16;279(29):30307-15. Epub 2004 May 11.

10.

Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.

Zollino M, Orteschi D, Ruiter M, Pfundt R, Steindl K, Cafiero C, Ricciardi S, Contaldo I, Chieffo D, Ranalli D, Acquafondata C, Murdolo M, Marangi G, Asaro A, Battaglia D.

Epilepsia. 2014 Jun;55(6):849-57. doi: 10.1111/epi.12617. Epub 2014 Apr 16.

PMID:
24738919
11.

Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome.

Andersen EF, Carey JC, Earl DL, Corzo D, Suttie M, Hammond P, South ST.

Eur J Hum Genet. 2014 Apr;22(4):464-70. doi: 10.1038/ejhg.2013.192. Epub 2013 Aug 21.

12.

Novel components of an active mitochondrial K(+)/H(+) exchange.

Zotova L, Aleschko M, Sponder G, Baumgartner R, Reipert S, Prinz M, Schweyen RJ, Nowikovsky K.

J Biol Chem. 2010 May 7;285(19):14399-414. doi: 10.1074/jbc.M109.059956. Epub 2010 Mar 2.

13.

LETM1-dependent mitochondrial Ca2+ flux modulates cellular bioenergetics and proliferation.

Doonan PJ, Chandramoorthy HC, Hoffman NE, Zhang X, Cárdenas C, Shanmughapriya S, Rajan S, Vallem S, Chen X, Foskett JK, Cheung JY, Houser SR, Madesh M.

FASEB J. 2014 Nov;28(11):4936-49. doi: 10.1096/fj.14-256453. Epub 2014 Jul 30.

PMID:
25077561
14.

Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion.

Roselló M, Monfort S, Orellana C, Ferrer-Bolufer I, Quiroga R, Oltra S, Martínez F.

Cytogenet Genome Res. 2009;125(2):103-8. doi: 10.1159/000227833. Epub 2009 Aug 31.

PMID:
19729912
15.

Electroneutral K+/H+ exchange in mitochondrial membrane vesicles involves Yol027/Letm1 proteins.

Froschauer E, Nowikovsky K, Schweyen RJ.

Biochim Biophys Acta. 2005 Jun 1;1711(1):41-8. Epub 2005 Mar 22.

16.

Association of mitochondrial letm1 with epileptic seizures.

Zhang X, Chen G, Lu Y, Liu J, Fang M, Luo J, Cao Q, Wang X.

Cereb Cortex. 2014 Oct;24(10):2533-40. doi: 10.1093/cercor/bht118. Epub 2013 May 3.

PMID:
23645710
17.
18.

Leucine zipper EF hand-containing transmembrane protein 1 (Letm1) and uncoupling proteins 2 and 3 (UCP2/3) contribute to two distinct mitochondrial Ca2+ uptake pathways.

Waldeck-Weiermair M, Jean-Quartier C, Rost R, Khan MJ, Vishnu N, Bondarenko AI, Imamura H, Malli R, Graier WF.

J Biol Chem. 2011 Aug 12;286(32):28444-55. doi: 10.1074/jbc.M111.244517. Epub 2011 May 25.

19.

Suppression of lung tumorigenesis by leucine zipper/EF hand-containing transmembrane-1.

Hwang SK, Piao L, Lim HT, Minai-Tehrani A, Yu KN, Ha YC, Chae CH, Lee KH, Beck GR, Park J, Cho MH.

PLoS One. 2010 Sep 2;5(9). pii: e12535. doi: 10.1371/journal.pone.0012535.

20.

Mdm38 interacts with ribosomes and is a component of the mitochondrial protein export machinery.

Frazier AE, Taylor RD, Mick DU, Warscheid B, Stoepel N, Meyer HE, Ryan MT, Guiard B, Rehling P.

J Cell Biol. 2006 Feb 13;172(4):553-64.

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