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Results: 1 to 20 of 79

Related Citations for PubMed (Select 21455166)

1.

Molecular genetics: The sound of silence.

Hurst LD.

Nature. 2011 Mar 31;471(7340):582-3. doi: 10.1038/471582a. No abstract available.

PMID:
21455166
2.

Listening to silence and understanding nonsense: exonic mutations that affect splicing.

Cartegni L, Chew SL, Krainer AR.

Nat Rev Genet. 2002 Apr;3(4):285-98. Review.

PMID:
11967553
3.

The power of point mutations.

Maquat LE.

Nat Genet. 2001 Jan;27(1):5-6. No abstract available.

PMID:
11137984
4.

Are splicing mutations the most frequent cause of hereditary disease?

López-Bigas N, Audit B, Ouzounis C, Parra G, Guigó R.

FEBS Lett. 2005 Mar 28;579(9):1900-3.

5.

Quantification of microRNAs, splicing isoforms, and homologous mRNAs with the invader assay.

Eis PS, Garcia-Blanco MA.

Methods Mol Biol. 2008;488:279-318. doi: 10.1007/978-1-60327-475-3_20.

PMID:
18982299
6.

Identification of cryptic splice site, exon skipping, and novel point mutations in type I CD36 deficiency.

Hanawa H, Watanabe K, Nakamura T, Ogawa Y, Toba K, Fuse I, Kodama M, Kato K, Fuse K, Aizawa Y.

J Med Genet. 2002 Apr;39(4):286-91. No abstract available.

7.

RNA interference: methylation mystery.

Ronemus M, Martienssen R.

Nature. 2005 Feb 3;433(7025):472-3. No abstract available.

PMID:
15690027
8.

A splicing mutation in RB1 in low penetrance retinoblastoma.

Schubert EL, Strong LC, Hansen MF.

Hum Genet. 1997 Oct;100(5-6):557-63.

PMID:
9341870
9.

The price of silent mutations.

Chamary JV, Hurst LD.

Sci Am. 2009 Jun;300(6):46-53. No abstract available.

PMID:
19485088
10.

Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.

Besana V, Di Pierro E, Brancaleoni V, Sabrina A, Fiocchi M, Cappellini MD.

Hum Genet. 2009 Apr;125(3):344. No abstract available.

PMID:
19320020
12.

[Analysis of the regulatory mechanism for the constitutive splicing using molecular genetics in fission yeast].

Haraguchi N, Tani T.

Tanpakushitsu Kakusan Koso. 2009 Dec;54(16 Suppl):2038-43. Review. Japanese. No abstract available.

PMID:
21089614
13.

Gene symbol: COL1A1. Disease: Osteogenesis imperfecta type I.

Schafer IA, Stein J, Hyland JC, Clark B.

Hum Genet. 2004 Mar;114(4):404. No abstract available.

PMID:
15046069
14.
15.

MicroRNAs: synthesis, mechanism, function, and recent clinical trials.

Wahid F, Shehzad A, Khan T, Kim YY.

Biochim Biophys Acta. 2010 Nov;1803(11):1231-43. doi: 10.1016/j.bbamcr.2010.06.013. Epub 2010 Jul 7. Review.

16.

The microRNA pathway and cancer.

Kwak PB, Iwasaki S, Tomari Y.

Cancer Sci. 2010 Nov;101(11):2309-15. doi: 10.1111/j.1349-7006.2010.01683.x. Review.

PMID:
20726859
17.

MicroRNAs repress mainly through mRNA decay.

Esslinger S, Förstemann K.

Angew Chem Int Ed Engl. 2009;48(5):853-5. doi: 10.1002/anie.200805127. No abstract available.

PMID:
19115352
18.

Micromanagement: a role for microRNAs in mRNA stability.

Roush SF, Slack FJ.

ACS Chem Biol. 2006 Apr 25;1(3):132-4.

PMID:
17163657
19.

Mechanisms of microRNA-mediated gene regulation in animal cells.

Nilsen TW.

Trends Genet. 2007 May;23(5):243-9. Epub 2007 Mar 26.

PMID:
17368621
20.

Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosis.

Highsmith WE Jr, Burch LH, Zhou Z, Olsen JC, Strong TV, Smith T, Friedman KJ, Silverman LM, Boucher RC, Collins FS, Knowles MR.

Hum Mutat. 1997;9(4):332-8.

PMID:
9101293
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