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Items: 1 to 20 of 42


Pathological and Surgical Observations on the Diseases of the ear.

Toynbee J.

Med Chir Trans. 1841;24:190-211. No abstract available.


Proteomic analysis of the balance between survival and cell death responses in cisplatin-mediated ototoxicity.

Jamesdaniel S, Ding D, Kermany MH, Davidson BA, Knight PR 3rd, Salvi R, Coling DE.

J Proteome Res. 2008 Aug;7(8):3516-24. doi: 10.1021/pr8002479. Epub 2008 Jun 26.


Relation between renin-angiotensin-aldosterone system and otosclerosis: a genetic association and in vitro study.

Imauchi Y, JeunemaƮtre X, Boussion M, Ferrary E, Sterkers O, Grayeli AB.

Otol Neurotol. 2008 Apr;29(3):295-301.


Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays.

Macgregor S, Zhao ZZ, Henders A, Nicholas MG, Montgomery GW, Visscher PM.

Nucleic Acids Res. 2008 Apr;36(6):e35. doi: 10.1093/nar/gkm1060. Epub 2008 Feb 14.


A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

Bel Hadj Ali I, Thys M, Beltaief N, Schrauwen I, Hilgert N, Vanderstraeten K, Dieltjens N, Mnif E, Hachicha S, Besbes G, Ben Arab S, Van Camp G.

Hum Genet. 2008 Apr;123(3):267-72. doi: 10.1007/s00439-008-0470-3. Epub 2008 Jan 26.


Association of bone morphogenetic proteins with otosclerosis.

Schrauwen I, Thys M, Vanderstraeten K, Fransen E, Dieltjens N, Huyghe JR, Ealy M, Claustres M, Cremers CR, Dhooge I, Declau F, Van de Heyning P, Vincent R, Somers T, Offeciers E, Smith RJ, Van Camp G.

J Bone Miner Res. 2008 Apr;23(4):507-16.


Fine mapping versus replication in whole-genome association studies.

Clarke GM, Carter KW, Palmer LJ, Morris AP, Cardon LR.

Am J Hum Genet. 2007 Nov;81(5):995-1005. Epub 2007 Sep 19.


Reelin signals survival through Src-family kinases that inactivate BAD activity.

Ohkubo N, Vitek MP, Morishima A, Suzuki Y, Miki T, Maeda N, Mitsuda N.

J Neurochem. 2007 Oct;103(2):820-30. Epub 2007 Aug 13.


The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations.

Thys M, Schrauwen I, Vanderstraeten K, Janssens K, Dieltjens N, Van Den Bogaert K, Fransen E, Chen W, Ealy M, Claustres M, Cremers CR, Dhooge I, Declau F, Claes J, Van de Heyning P, Vincent R, Somers T, Offeciers E, Smith RJ, Van Camp G.

Hum Mol Genet. 2007 Sep 1;16(17):2021-30. Epub 2007 Jun 22.


Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis.

Chen W, Meyer NC, McKenna MJ, Pfister M, McBride DJ Jr, Fukushima K, Thys M, Camp GV, Smith RJ.

Clin Genet. 2007 May;71(5):406-14.


qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data.

Hellemans J, Mortier G, De Paepe A, Speleman F, Vandesompele J.

Genome Biol. 2007;8(2):R19.


A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.

Thys M, Van Den Bogaert K, Iliadou V, Vanderstraeten K, Dieltjens N, Schrauwen I, Chen W, Eleftheriades N, Grigoriadou M, Pauw RJ, Cremers CR, Smith RJ, Petersen MB, Van Camp G.

Eur J Hum Genet. 2007 Mar;15(3):362-8. Epub 2007 Jan 10.


Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies.

Pearson JV, Huentelman MJ, Halperin RF, Tembe WD, Melquist S, Homer N, Brun M, Szelinger S, Coon KD, Zismann VL, Webster JA, Beach T, Sando SB, Aasly JO, Heun R, Jessen F, Kolsch H, Tsolaki M, Daniilidou M, Reiman EM, Papassotiropoulos A, Hutton ML, Stephan DA, Craig DW.

Am J Hum Genet. 2007 Jan;80(1):126-39. Epub 2006 Dec 6.


Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus.

Brownstein Z, Goldfarb A, Levi H, Frydman M, Avraham KB.

Arch Otolaryngol Head Neck Surg. 2006 Apr;132(4):416-24.


A haplotype map of the human genome.

International HapMap Consortium.

Nature. 2005 Oct 27;437(7063):1299-320.


Efficiency and power in genetic association studies.

de Bakker PI, Yelensky R, Pe'er I, Gabriel SB, Daly MJ, Altshuler D.

Nat Genet. 2005 Nov;37(11):1217-23. Epub 2005 Oct 23.


Design of case-controls studies with unscreened controls.

Moskvina V, Holmans P, Schmidt KM, Craddock N.

Ann Hum Genet. 2005 Sep;69(Pt 5):566-76.


On the interpretation of genetic association studies.

Kathiresan S, Newton-Cheh C, Gerszten RE.

Eur Heart J. 2004 Aug;25(16):1378-81. No abstract available.


Haploview: analysis and visualization of LD and haplotype maps.

Barrett JC, Fry B, Maller J, Daly MJ.

Bioinformatics. 2005 Jan 15;21(2):263-5. Epub 2004 Aug 5.


The future of association studies: gene-based analysis and replication.

Neale BM, Sham PC.

Am J Hum Genet. 2004 Sep;75(3):353-62. Epub 2004 Jul 22.

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