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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2004 | 1 |
2005 | 1 |
2009 | 3 |
2018 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 20589
6 results
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Impaired Local Translation of β-actin mRNA in Ighmbp2-Deficient Motoneurons: Implications for Spinal Muscular Atrophy with respiratory Distress (SMARD1).
Neuroscience. 2018 Aug 21;386:24-40. doi: 10.1016/j.neuroscience.2018.06.019. Epub 2018 Jun 19.
Neuroscience. 2018.
PMID: 29928949
Devastation of bone tissue in the appendicular skeleton parallels the progression of neuromuscular disease.
Lee BJ, Cox GA, Maddatu TP, Judex S, Rubin CT.
Lee BJ, et al.
J Musculoskelet Neuronal Interact. 2009 Oct-Dec;9(4):215-24.
J Musculoskelet Neuronal Interact. 2009.
PMID: 19949279
Free article.
Item in Clipboard
Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery.
de Planell-Saguer M, Schroeder DG, Rodicio MC, Cox GA, Mourelatos Z.
de Planell-Saguer M, et al.
Hum Mol Genet. 2009 Jun 15;18(12):2115-26. doi: 10.1093/hmg/ddp134. Epub 2009 Mar 19.
Hum Mol Genet. 2009.
PMID: 19299493
Free PMC article.
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IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1).
Guenther UP, Handoko L, Laggerbauer B, Jablonka S, Chari A, Alzheimer M, Ohmer J, Plöttner O, Gehring N, Sickmann A, von Au K, Schuelke M, Fischer U.
Guenther UP, et al.
Hum Mol Genet. 2009 Apr 1;18(7):1288-300. doi: 10.1093/hmg/ddp028. Epub 2009 Jan 20.
Hum Mol Genet. 2009.
PMID: 19158098
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Dilated cardiomyopathy in the nmd mouse: transgenic rescue and QTLs that improve cardiac function and survival.
Maddatu TP, Garvey SM, Schroeder DG, Zhang W, Kim SY, Nicholson AI, Davis CJ, Cox GA.
Maddatu TP, et al.
Hum Mol Genet. 2005 Nov 1;14(21):3179-89. doi: 10.1093/hmg/ddi349. Epub 2005 Sep 20.
Hum Mol Genet. 2005.
PMID: 16174646
Free PMC article.
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Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M.
Grohmann K, et al.
Hum Mol Genet. 2004 Sep 15;13(18):2031-42. doi: 10.1093/hmg/ddh222. Epub 2004 Jul 21.
Hum Mol Genet. 2004.
PMID: 15269181
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