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Items: 1 to 20 of 79


The Effect of PCDH15 Gene Variations on the Risk of Noise-induced Hearing Loss in a Chinese Population.

Xu XR, Wang JJ, Yang QY, Jiao J, He LH, Yu SF, Gu GZ, Chen GS, Zhou WH, Wu H, Li YH, Zhang HL, Zhang ZR, Jin XN.

Biomed Environ Sci. 2017 Feb;30(2):143-146. doi: 10.3967/bes2017.019.


Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.

Wang R, Han S, Khan A, Zhang X.

Genet Test Mol Biomarkers. 2017 May;21(5):316-321. doi: 10.1089/gtmb.2016.0328. Epub 2017 Mar 10.


A Partial Calcium-Free Linker Confers Flexibility to Inner-Ear Protocadherin-15.

Powers RE, Gaudet R, Sotomayor M.

Structure. 2017 Mar 7;25(3):482-495. doi: 10.1016/j.str.2017.01.014. Epub 2017 Feb 23.


Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.

Lo MT, Hinds DA, Tung JY, Franz C, Fan CC, Wang Y, Smeland OB, Schork A, Holland D, Kauppi K, Sanyal N, Escott-Price V, Smith DJ, O'Donovan M, Stefansson H, Bjornsdottir G, Thorgeirsson TE, Stefansson K, McEvoy LK, Dale AM, Andreassen OA, Chen CH.

Nat Genet. 2017 Jan;49(1):152-156. doi: 10.1038/ng.3736. Epub 2016 Dec 5.


Plasma Membrane Targeting of Protocadherin 15 Is Regulated by the Golgi-Associated Chaperone Protein PIST.

Nie H, Liu Y, Yin X, Cao H, Wang Y, Xiong W, Lin Y, Xu Z.

Neural Plast. 2016;2016:8580675. Epub 2016 Oct 27.


Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi Arabia.

Dallol A, Daghistani K, Elaimi A, Al-Wazani WA, Bamanie A, Safiah M, Sagaty S, Taha L, Zahed R, Bajouh O, Chaudhary AG, Gari MA, Turki R, Al-Qahtani MH, Abuzenadah AM.

BMC Med Genet. 2016 Oct 10;17(Suppl 1):67.


Discovery of novel plasma proteins as biomarkers for the development of incisional hernias after midline incision in patients with colorectal cancer: The ColoCare study.

Böhm J, Pianka F, Stüttgen N, Rho J, Gigic B, Zhang Y, Habermann N, Schrotz-King P, Abbenhardt-Martin C, Zielske L, Lampe PD, Ulrich A, Diener MK, Ulrich CM.

Surgery. 2017 Mar;161(3):808-817. doi: 10.1016/j.surg.2016.08.025. Epub 2016 Oct 13.


Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.

Chen S, Dong C, Wang Q, Zhong Z, Qi Y, Ke X, Liu Y.

Genet Test Mol Biomarkers. 2016 Nov;20(11):660-665. Epub 2016 Sep 9.


Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.

Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, Petit C.

PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016.


Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.

Ishizuka K, Kimura H, Wang C, Xing J, Kushima I, Arioka Y, Oya-Ito T, Uno Y, Okada T, Mori D, Aleksic B, Ozaki N.

PLoS One. 2016 Apr 8;11(4):e0153224. doi: 10.1371/journal.pone.0153224. eCollection 2016.


MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.

Grati M, Yan D, Raval MH, Walsh T, Ma Q, Chakchouk I, Kannan-Sundhari A, Mittal R, Masmoudi S, Blanton SH, Tekin M, King MC, Yengo CM, Liu XZ.

Hum Mutat. 2016 May;37(5):481-7. doi: 10.1002/humu.22961. Epub 2016 Feb 16.


Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing.

Yoshimura H, Miyagawa M, Kumakawa K, Nishio SY, Usami S.

J Hum Genet. 2016 May;61(5):419-22. doi: 10.1038/jhg.2015.168. Epub 2016 Jan 21.


High-throughput alternative splicing detection using dually constrained correspondence analysis (DCCA).

Baty F, Klingbiel D, Zappa F, Brutsche M.

J Biomed Inform. 2015 Dec;58:175-185. doi: 10.1016/j.jbi.2015.10.002. Epub 2015 Oct 19.


Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.

Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H.

J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7.


Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.

Xie G, Myint PK, Voora D, Laskowitz DT, Shi P, Ren F, Wang H, Yang Y, Huo Y, Gao W, Wu Y.

Atherosclerosis. 2015 Nov;243(1):30-7. doi: 10.1016/j.atherosclerosis.2015.08.034. Epub 2015 Sep 5.


Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.

Jiang L, Liang X, Li Y, Wang J, Zaneveld JE, Wang H, Xu S, Wang K, Wang B, Chen R, Sui R.

Orphanet J Rare Dis. 2015 Sep 4;10:110. doi: 10.1186/s13023-015-0329-3.


Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss.

Chen DY, Zhu WD, Chai YC, Chen Y, Sun L, Yang T, Wu H.

Int J Pediatr Otorhinolaryngol. 2015 Oct;79(10):1654-7. doi: 10.1016/j.ijporl.2015.07.008. Epub 2015 Jul 11.


Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing.

Wu CC, Lin YH, Liu TC, Lin KN, Yang WS, Hsu CJ, Chen PL, Wu CM.

Medicine (Baltimore). 2015 Jul;94(27):e1073. doi: 10.1097/MD.0000000000001073.


The tip-link molecular complex of the auditory mechano-electrical transduction machinery.

Pepermans E, Petit C.

Hear Res. 2015 Dec;330(Pt A):10-7. doi: 10.1016/j.heares.2015.05.005. Epub 2015 Jun 3. Review.


Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.

Chen Y, Wang Z, Wang Z, Chen D, Chai Y, Pang X, Sun L, Wang X, Yang T, Wu H.

PLoS One. 2015 May 26;10(5):e0127879. doi: 10.1371/journal.pone.0127879. eCollection 2015.

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