A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
Cheng, J, Han, DY, Dai, P, Sun, HJ, Tao, R, Sun, Q, Yan, D, Qin, W, Wang, HY, Ouyang, XM, Yang, SZ, Cao, JY, Feng, GY, Du, LL, Zhang, YZ, Zhai, SQ, Yang, WY, Liu, XZ, He, L, Yuan, HJ
Published in Clinical genetics (01.11.2007)
Published in Clinical genetics (01.11.2007)
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Journal Article
Hypoxia-Inducible Factor 1-Alpha Reduces Infarction and Attenuates Progression of Cardiac Dysfunction After Myocardial Infarction in the Mouse
Kido, Masakuni, Du, Lingling, Sullivan, Christopher C., Li, Xiaodong, Deutsch, Reena, Jamieson, Stuart W., Thistlethwaite, Patricia A.
Published in Journal of the American College of Cardiology (06.12.2005)
Published in Journal of the American College of Cardiology (06.12.2005)
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Journal Article
Swi1 Prevents Replication Fork Collapse and Controls Checkpoint Kinase Cds1
Noguchi, Eishi, Noguchi, Chiaki, Du, Li-Lin, Russell, Paul
Published in Molecular and Cellular Biology (01.11.2003)
Published in Molecular and Cellular Biology (01.11.2003)
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Journal Article
Cdc42 Interacts with the Exocyst and Regulates Polarized Secretion
Zhang, Xiaoyu, Bi, Erfei, Novick, Peter, Du, Lilin, Kozminski, Keith G., Lipschutz, Joshua H., Guo, Wei
Published in The Journal of biological chemistry (14.12.2001)
Published in The Journal of biological chemistry (14.12.2001)
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Journal Article
Outcomes of pulmonary endarterectomy for treatment of extreme thromboembolic pulmonary hypertension
Thistlethwaite, Patricia A., Kemp, Aaron, Du, Lingling, Madani, Michael M., Jamieson, Stuart W.
Published in The Journal of thoracic and cardiovascular surgery (01.02.2006)
Published in The Journal of thoracic and cardiovascular surgery (01.02.2006)
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Journal Article
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans
Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, Johnson, Kenneth R., Liu, Xue Zhong
Published in Human molecular genetics (01.01.2005)
Published in Human molecular genetics (01.01.2005)
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Journal Article
Induction of Pulmonary Hypertension by an Angiopoietin 1/TIE2/Serotonin Pathway
Sullivan, Christopher C., Du, Lingling, Chu, Danny, Cho, Augustine J., Kido, Masakuni, Wolf, Paul L., Jamieson, Stuart W., Thistlethwaite, Patricia A.
Published in Proceedings of the National Academy of Sciences - PNAS (14.10.2003)
Published in Proceedings of the National Academy of Sciences - PNAS (14.10.2003)
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Journal Article
Serum levels of leptin, insulin, and lipids in relation to breast cancer in china
Han, Cunzhi, Zhang, Hong-Tao, Du, Lili, Liu, Xiuying, Jing, Jiexian, Zhao, Xianwen, Yang, Xuan, Tian, Baoguo
Published in Endocrine (01.02.2005)
Published in Endocrine (01.02.2005)
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Journal Article
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
Liu, Xue Zhong, Ouyang, Xiao Mei, Xia, Xia Juan, Zheng, Jing, Pandya, Arti, Li, Fang, Du, Li Lin, Welch, Katherine O., Petit, Christine, Smith, Richard J.H., Webb, Bradley T., Yan, Denise, Arnos, Kathleen S., Corey, David, Dallos, Peter, Nance, Walter E., Chen, Zheng Yi
Published in Human molecular genetics (15.05.2003)
Published in Human molecular genetics (15.05.2003)
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Journal Article
Retention but Not Recruitment of Crb2 at Double-Strand Breaks Requires Rad1 and Rad3 Complexes
Du, Li-Lin, Nakamura, Toru M., Moser, Bettina A., Russell, Paul
Published in Molecular and Cellular Biology (01.09.2003)
Published in Molecular and Cellular Biology (01.09.2003)
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Journal Article
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
XIAO MEI OUYANG, YAN, Denise, BROWN, Steve D. M, BALKANY, Thomas, XUE ZHONG LIU, LI LIN DU, FIELDING HEJTMANCIK, J, JACOBSON, Samuel G, NANCE, Walter E, LI, An Ren, ANGELI, Simon, KAISER, Muriel, NEWTON, Valerie
Published in Human genetics (01.03.2005)
Published in Human genetics (01.03.2005)
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Journal Article
The prevalence of connexin 26 (GJB2) mutations in the Chinese population
XUE ZHONG LIU, XIA JUAN XIA, LI RONG XU, XIAO MEI KE, XIAO MEI OUYANG, LI LIN DU, YU HE LIU, ANGELI, Simon, TELISCHI, Fred F, NANCE, Walter E, BALKANY, Thomas
Published in Human genetics (01.10.2002)
Published in Human genetics (01.10.2002)
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Journal Article
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians
YAN, Denise, PARK, Hong-Joon, XUE ZHONG LIU, XIAO MEI OUYANG, PANDYA, Arti, DOI, Katsumi, ERDENETUNGALAG, Raadnabazar, LI LIN DU, MATSUSHIRO, Naoki, NANCE, Walter E, GRIFFITH, Andrew J
Published in Human genetics (01.12.2003)
Published in Human genetics (01.12.2003)
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Journal Article
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness
XIAO MEI OUYANG, XIA JUAN XIA, VERPY, Elisabeth, LI LIN DU, PANDYA, Arti, PETIT, Christine, BALKANY, Thomas, NANCE, Walter E, XUE ZHONG LIU
Published in Human genetics (01.07.2002)
Published in Human genetics (01.07.2002)
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Journal Article
Differential Myocardial Gene Delivery by Recombinant Serotype-Specific Adeno-associated Viral Vectors
Du, Lingling, Kido, Masakuni, Lee, Darwin V, Rabinowitz, Joseph E, Samulski, R Jude, Jamieson, Stuart W, Weitzman, Matthew D, Thistlethwaite, Patricia A
Published in Molecular therapy (01.09.2004)
Published in Molecular therapy (01.09.2004)
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Journal Article
Homo-oligomerization Is the Essential Function of the Tandem BRCT Domains in the Checkpoint Protein Crb2
Du, Li-Lin, Moser, Bettina A., Russell, Paul
Published in The Journal of biological chemistry (10.09.2004)
Published in The Journal of biological chemistry (10.09.2004)
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Journal Article