Cao L - Search Results

1

Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory.

Cao L, Molina J, Abad C, Carmona-Mora P, Cárdenas Oyarzo A, Young JI, Walz K. Cao L, et al. Hum Mol Genet. 2014 Apr 1;23(7):1771-82. doi: 10.1093/hmg/ddt568. Epub 2013 Nov 11. Hum Mol Genet. 2014. PMID: 24218365

2

Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome.

Carmona-Mora P, Encina CA, Canales CP, Cao L, Molina J, Kairath P, Young JI, Walz K. Carmona-Mora P, et al. Among authors: cao l. BMC Mol Biol. 2010 Aug 25;11:63. doi: 10.1186/1471-2199-11-63. BMC Mol Biol. 2010. PMID: 20738874 Free PMC article.

3

Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith-Magenis syndrome.

Vieira GH, Rodriguez JD, Carmona-Mora P, Cao L, Gamba BF, Carvalho DR, de Rezende Duarte A, Santos SR, de Souza DH, DuPont BR, Walz K, Moretti-Ferreira D, Srivastava AK. Vieira GH, et al. Among authors: cao l. Eur J Hum Genet. 2012 Feb;20(2):148-54. doi: 10.1038/ejhg.2011.167. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897445 Free PMC article.

4

RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome.

Carmona-Mora P, Canales CP, Cao L, Perez IC, Srivastava AK, Young JI, Walz K. Carmona-Mora P, et al. Among authors: cao l. PLoS One. 2012;7(9):e45155. doi: 10.1371/journal.pone.0045155. Epub 2012 Sep 18. PLoS One. 2012. PMID: 23028815 Free PMC article.

5

Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.

Camarena V, Cao L, Abad C, Abrams A, Toledo Y, Araki K, Araki M, Walz K, Young JI. Camarena V, et al. Among authors: cao l. EMBO Mol Med. 2014 Aug;6(8):1003-15. doi: 10.15252/emmm.201404044. EMBO Mol Med. 2014. PMID: 25001218 Free PMC article.

6

A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation.

Abad C, Cook MM, Cao L, Jones JR, Rao NR, Dukes-Rimsky L, Pauly R, Skinner C, Wang Y, Luo F, Stevenson RE, Walz K, Srivastava AK. Abad C, et al. Among authors: cao l. Biology (Basel). 2018 May 24;7(2):31. doi: 10.3390/biology7020031. Biology (Basel). 2018. PMID: 29794985 Free PMC article.

7

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.

Diaz-Horta O, Subasioglu-Uzak A, Grati M, DeSmidt A, Foster J 2nd, Cao L, Bademci G, Tokgoz-Yilmaz S, Duman D, Cengiz FB, Abad C, Mittal R, Blanton S, Liu XZ, Farooq A, Walz K, Lu Z, Tekin M. Diaz-Horta O, et al. Among authors: cao l. Proc Natl Acad Sci U S A. 2014 Jul 8;111(27):9864-8. doi: 10.1073/pnas.1401950111. Epub 2014 Jun 23. Proc Natl Acad Sci U S A. 2014. PMID: 24958875 Free PMC article.

8

Comparing different timings of tourniquet application in total knee arthroplasty: effects on postoperative pain and bone cement interface.

Wu W, Cao L, Sun K, Wang H. Wu W, et al. Among authors: cao l. J Orthop Surg Res. 2025 Jan 17;20(1):59. doi: 10.1186/s13018-025-05486-9. J Orthop Surg Res. 2025. PMID: 39825387 Clinical Trial.

9

Biomimetic wrinkled prebiotic microspheres with enhanced intestinal retention for hyperphosphatemia and vascular calcification.

Hu B, Wang Y, Yu L, Cao L, Liu S, Zhong L, Wang G, Qiu X, Hou H. Hu B, et al. Among authors: cao l. Sci Adv. 2025 Jan 17;11(3):eads5286. doi: 10.1126/sciadv.ads5286. Epub 2025 Jan 17. Sci Adv. 2025. PMID: 39823333

10

Unique ultrastructural organization of human rod photoreceptors.

Lewis TR, Klementieva NV, Phan S, Castillo CM, Kim KY, Cao LY, Ellisman MH, Arshavsky VY, Alekseev O. Lewis TR, et al. Among authors: cao ly. Commun Biol. 2025 Jan 16;8(1):63. doi: 10.1038/s42003-025-07473-6. Commun Biol. 2025. PMID: 39820780

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