Similar articles for PMID: 15565545

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1971	1
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2005	12
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1

mRNA Metabolism and hereditary disorders: a tale of surveillance and escape.

Neu-Yilik G, Kulozik AE. Neu-Yilik G, et al. Klin Padiatr. 2004 Nov-Dec;216(6):304-14. doi: 10.1055/s-2004-832337. Klin Padiatr. 2004. PMID: 15565545 Review.

2

Nucleotide sequence determines the accelerated rate of point mutations.

Kini RM, Chinnasamy A. Kini RM, et al. Toxicon. 2010 Sep 1;56(3):295-304. doi: 10.1016/j.toxicon.2009.12.022. Epub 2010 Apr 1. Toxicon. 2010. PMID: 20362603

3

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

4

Alternative splicing and nonsense-mediated mRNA decay regulate mammalian ribosomal gene expression.

Cuccurese M, Russo G, Russo A, Pietropaolo C. Cuccurese M, et al. Nucleic Acids Res. 2005 Oct 27;33(18):5965-77. doi: 10.1093/nar/gki905. Print 2005. Nucleic Acids Res. 2005. PMID: 16254077 Free PMC article.

5

Characterization and functional significance of myotrophin: a gene with multiple transcripts.

Adhikary G, Gupta S, Sil P, Saad Y, Sen S. Adhikary G, et al. Gene. 2005 Jun 20;353(1):31-40. doi: 10.1016/j.gene.2005.03.045. Gene. 2005. PMID: 15946807

6

Disease-causing mutations improving the branch site and polypyrimidine tract: pseudoexon activation of LINE-2 and antisense Alu lacking the poly(T)-tail.

Meili D, Kralovicova J, Zagalak J, Bonafé L, Fiori L, Blau N, Thöny B, Vorechovsky I. Meili D, et al. Hum Mutat. 2009 May;30(5):823-31. doi: 10.1002/humu.20969. Hum Mutat. 2009. PMID: 19280650

7

RNA-protein interactions and control of mRNA stability in neurons.

Bolognani F, Perrone-Bizzozero NI. Bolognani F, et al. J Neurosci Res. 2008 Feb 15;86(3):481-9. doi: 10.1002/jnr.21473. J Neurosci Res. 2008. PMID: 17853436 Review.

8

The meaning of nonsense.

Stalder L, Mühlemann O. Stalder L, et al. Trends Cell Biol. 2008 Jul;18(7):315-21. doi: 10.1016/j.tcb.2008.04.005. Epub 2008 Jun 2. Trends Cell Biol. 2008. PMID: 18524595 Review.

9

Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).

Bergmann C, Küpper F, Schmitt CP, Vester U, Neuhaus TJ, Senderek J, Zerres K. Bergmann C, et al. J Med Genet. 2005 Oct;42(10):e63. doi: 10.1136/jmg.2005.032318. J Med Genet. 2005. PMID: 16199545 Free PMC article.

10

Structure of the bovine VASAP-60/PRKCSH gene, functional analysis of the promoter, and gene expression analysis.

Brûlé S, Sayasith K, Sirois J, Silversides DW, Lussier JG. Brûlé S, et al. Gene. 2007 Apr 15;391(1-2):63-75. doi: 10.1016/j.gene.2006.12.012. Epub 2006 Dec 22. Gene. 2007. PMID: 17250974

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