Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 17

1.

Porcine methionine sulfoxide reductase B3: molecular cloning, tissue-specific expression profiles, and polymorphisms associated with ear size in Sus scrofa.

Zhang Y, Liang J, Zhang L, Wang L, Liu X, Yan H, Zhao K, Shi H, Zhang T, Li N, Pu L, Wang L.

J Anim Sci Biotechnol. 2015 Dec 30;6:60. doi: 10.1186/s40104-015-0060-x. eCollection 2015.

2.

Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing Impairment.

Wang HY, Zhao YL, Liu Q, Yuan H, Gao Y, Lan L, Yu L, Wang DY, Guan J, Wang QJ.

Chin Med J (Engl). 2015 Dec 20;128(24):3345-51. doi: 10.4103/0366-6999.171440.

3.

12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region.

Mc Cormack A, Sharpe C, Gregersen N, Smith W, Hayes I, George AM, Love DR.

Case Rep Genet. 2015;2015:192071. doi: 10.1155/2015/192071. Epub 2015 Jul 22.

4.

The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways.

Van Rossom S, Op de Beeck K, Hristovska V, Winderickx J, Van Camp G.

Front Cell Neurosci. 2015 Jul 16;9:231. doi: 10.3389/fncel.2015.00231. eCollection 2015.

5.

Linked genetic variants on chromosome 10 control ear morphology and body mass among dog breeds.

Webster MT, Kamgari N, Perloski M, Hoeppner MP, Axelsson E, Hedhammar Å, Pielberg G, Lindblad-Toh K.

BMC Genomics. 2015 Jun 23;16:474. doi: 10.1186/s12864-015-1702-2.

6.

Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.

Shafique S, Siddiqi S, Schraders M, Oostrik J, Ayub H, Bilal A, Ajmal M, Seco CZ, Strom TM, Mansoor A, Mazhar K, Shah ST, Hussain A, Azam M, Kremer H, Qamar R.

PLoS One. 2014 Jun 20;9(6):e100146. doi: 10.1371/journal.pone.0100146. eCollection 2014.

7.

Large-effect pleiotropic or closely linked QTL segregate within and across ten US cattle breeds.

Saatchi M, Schnabel RD, Taylor JF, Garrick DJ.

BMC Genomics. 2014 Jun 6;15:442. doi: 10.1186/1471-2164-15-442.

8.

Control of mitochondrial integrity in ageing and disease.

Szklarczyk R, Nooteboom M, Osiewacz HD.

Philos Trans R Soc Lond B Biol Sci. 2014 Jul 5;369(1646):20130439. doi: 10.1098/rstb.2013.0439. Review.

9.

Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89.

Santos-Cortez RL, Lee K, Azeem Z, Antonellis PJ, Pollock LM, Khan S, Irfanullah, Andrade-Elizondo PB, Chiu I, Adams MD, Basit S, Smith JD; University of Washington Center for Mendelian Genomics, Nickerson DA, McDermott BM Jr, Ahmad W, Leal SM.

Am J Hum Genet. 2013 Jul 11;93(1):132-40. doi: 10.1016/j.ajhg.2013.05.018. Epub 2013 Jun 13.

10.

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.

von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, Nürnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, Nürnberg P, Hofmann K, Richardson GP, Hammerschmidt M, Moser T, Wollnik B, Koehler CM, Teitell MA, Barakat A, Kubisch C.

Am J Hum Genet. 2012 Nov 2;91(5):919-27. doi: 10.1016/j.ajhg.2012.09.002. Epub 2012 Oct 18.

11.

Genetics: advances in genetic testing for deafness.

Shearer AE, Smith RJ.

Curr Opin Pediatr. 2012 Dec;24(6):679-86. doi: 10.1097/MOP.0b013e3283588f5e. Review.

12.

Autosomal recessive nonsyndromic deafness genes: a review.

Duman D, Tekin M.

Front Biosci (Landmark Ed). 2012 Jun 1;17:2213-36. Review.

13.

Cardiovascular redox and ox stress proteomics.

Kumar V, Calamaras TD, Haeussler D, Colucci WS, Cohen RA, McComb ME, Pimentel D, Bachschmid MM.

Antioxid Redox Signal. 2012 Dec 1;17(11):1528-59. Epub 2012 Aug 10. Review.

14.

DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth.

Lee H, Jaffe AE, Feinberg JI, Tryggvadottir R, Brown S, Montano C, Aryee MJ, Irizarry RA, Herbstman J, Witter FR, Goldman LR, Feinberg AP, Fallin MD.

Int J Epidemiol. 2012 Feb;41(1):188-99. doi: 10.1093/ije/dyr237.

15.

DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.

Ali RA, Rehman AU, Khan SN, Husnain T, Riazuddin S, Friedman TB, Ahmed ZM, Riazuddin S.

Clin Genet. 2012 May;81(5):498-500. doi: 10.1111/j.1399-0004.2011.01729.x. Epub 2011 Dec 28. No abstract available.

16.

Deafness in the genomics era.

Shearer AE, Hildebrand MS, Sloan CM, Smith RJ.

Hear Res. 2011 Dec;282(1-2):1-9. doi: 10.1016/j.heares.2011.10.001. Epub 2011 Oct 8. Review.

17.

Apoptosis in acquired and genetic hearing impairment: the programmed death of the hair cell.

Op de Beeck K, Schacht J, Van Camp G.

Hear Res. 2011 Nov;281(1-2):18-27. doi: 10.1016/j.heares.2011.07.002. Epub 2011 Jul 18. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk