Li T - Search Results

1

Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis.

Rachel RA, May-Simera HL, Veleri S, Gotoh N, Choi BY, Murga-Zamalloa C, McIntyre JC, Marek J, Lopez I, Hackett AN, Zhang J, Brooks M, den Hollander AI, Beales PL, Li T, Jacobson SG, Sood R, Martens JR, Liu P, Friedman TB, Khanna H, Koenekoop RK, Kelley MW, Swaroop A. Rachel RA, et al. Among authors: li t. J Clin Invest. 2012 Apr;122(4):1233-45. doi: 10.1172/JCI60981. Epub 2012 Mar 26. J Clin Invest. 2012. PMID: 22446187 Free PMC article.

2

Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma.

Liu C, Bakeri H, Li T, Swaroop A. Liu C, et al. Among authors: li t. Hum Mol Genet. 2012 Apr 15;21(8):1848-60. doi: 10.1093/hmg/ddr616. Epub 2012 Jan 6. Hum Mol Genet. 2012. PMID: 22228100 Free PMC article.

3

Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins.

Rachel RA, Li T, Swaroop A. Rachel RA, et al. Among authors: li t. Cilia. 2012 Dec 3;1(1):22. doi: 10.1186/2046-2530-1-22. Cilia. 2012. PMID: 23351659 Free PMC article.

4

Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesis.

Liu C, Lin C, Whitaker DT, Bakeri H, Bulgakov OV, Liu P, Lei J, Dong L, Li T, Swaroop A. Liu C, et al. Among authors: li t. Hum Mol Genet. 2013 Jun 1;22(11):2234-46. doi: 10.1093/hmg/ddt075. Epub 2013 Feb 18. Hum Mol Genet. 2013. PMID: 23420014 Free PMC article.

5

Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis.

Veleri S, Manjunath SH, Fariss RN, May-Simera H, Brooks M, Foskett TA, Gao C, Longo TA, Liu P, Nagashima K, Rachel RA, Li T, Dong L, Swaroop A. Veleri S, et al. Among authors: li t. Nat Commun. 2014 Jun 20;5:4207. doi: 10.1038/ncomms5207. Nat Commun. 2014. PMID: 24947469 Free PMC article.

6

Null and hypomorph Prickle1 alleles in mice phenocopy human Robinow syndrome and disrupt signaling downstream of Wnt5a.

Liu C, Lin C, Gao C, May-Simera H, Swaroop A, Li T. Liu C, et al. Among authors: li t. Biol Open. 2014 Sep 4;3(9):861-70. doi: 10.1242/bio.20148375. Biol Open. 2014. PMID: 25190059 Free PMC article.

7

Leber congenital amaurosis caused by mutations in RPGRIP1.

Li T. Li T. Cold Spring Harb Perspect Med. 2014 Nov 20;5(4):a017384. doi: 10.1101/cshperspect.a017384. Cold Spring Harb Perspect Med. 2014. PMID: 25414380 Free PMC article. Review.

8

CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies.

Rachel RA, Yamamoto EA, Dewanjee MK, May-Simera HL, Sergeev YV, Hackett AN, Pohida K, Munasinghe J, Gotoh N, Wickstead B, Fariss RN, Dong L, Li T, Swaroop A. Rachel RA, et al. Among authors: li t. Hum Mol Genet. 2015 Jul 1;24(13):3775-91. doi: 10.1093/hmg/ddv123. Epub 2015 Apr 9. Hum Mol Genet. 2015. PMID: 25859007 Free PMC article.

9

A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration.

Wu Z, Hiriyanna S, Qian H, Mookherjee S, Campos MM, Gao C, Fariss R, Sieving PA, Li T, Colosi P, Swaroop A. Wu Z, et al. Among authors: li t. Hum Mol Genet. 2015 Jul 15;24(14):3956-70. doi: 10.1093/hmg/ddv134. Epub 2015 Apr 15. Hum Mol Genet. 2015. PMID: 25877300 Free PMC article.

10

Long-term rescue of cone photoreceptor degeneration in retinitis pigmentosa 2 (RP2)-knockout mice by gene replacement therapy.

Mookherjee S, Hiriyanna S, Kaneshiro K, Li L, Li Y, Li W, Qian H, Li T, Khanna H, Colosi P, Swaroop A, Wu Z. Mookherjee S, et al. Among authors: li t, li y, li w, li l. Hum Mol Genet. 2015 Nov 15;24(22):6446-58. doi: 10.1093/hmg/ddv354. Epub 2015 Sep 10. Hum Mol Genet. 2015. PMID: 26358772 Free PMC article.

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