Lin CS - Search Results

1

Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype.

Adebola AA, Di Castri T, He CZ, Salvatierra LA, Zhao J, Brown K, Lin CS, Worman HJ, Liem RK. Adebola AA, et al. Among authors: lin cs. Hum Mol Genet. 2015 Apr 15;24(8):2163-74. doi: 10.1093/hmg/ddu736. Epub 2014 Dec 30. Hum Mol Genet. 2015. PMID: 25552649 Free PMC article.

2

The role of microtubule actin cross-linking factor 1 (MACF1) in the Wnt signaling pathway.

Chen HJ, Lin CM, Lin CS, Perez-Olle R, Leung CL, Liem RK. Chen HJ, et al. Among authors: lin cs, lin cm. Genes Dev. 2006 Jul 15;20(14):1933-45. doi: 10.1101/gad.1411206. Epub 2006 Jun 30. Genes Dev. 2006. PMID: 16815997 Free PMC article.

3

Nervous-tissue-specific elimination of microtubule-actin crosslinking factor 1a results in multiple developmental defects in the mouse brain.

Goryunov D, He CZ, Lin CS, Leung CL, Liem RK. Goryunov D, et al. Among authors: lin cs. Mol Cell Neurosci. 2010 May;44(1):1-14. doi: 10.1016/j.mcn.2010.01.010. Epub 2010 Feb 17. Mol Cell Neurosci. 2010. PMID: 20170731 Free PMC article.

4

CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model.

Wert KJ, Bassuk AG, Wu WH, Gakhar L, Coglan D, Mahajan M, Wu S, Yang J, Lin CS, Tsang SH, Mahajan VB. Wert KJ, et al. Among authors: lin cs. Hum Mol Genet. 2015 Aug 15;24(16):4584-98. doi: 10.1093/hmg/ddv189. Epub 2015 May 20. Hum Mol Genet. 2015. PMID: 25994508 Free PMC article.

5

Abolishing the prelamin A ZMPSTE24 cleavage site leads to progeroid phenotypes with near-normal longevity in mice.

Wang Y, Shilagardi K, Hsu T, Odinammadu KO, Maruyama T, Wu W, Lin CS, Damoci CB, Spear ED, Shin JY, Hsu W, Michaelis S, Worman HJ. Wang Y, et al. Among authors: lin cs. Proc Natl Acad Sci U S A. 2022 Mar 1;119(9):e2118695119. doi: 10.1073/pnas.2118695119. Proc Natl Acad Sci U S A. 2022. PMID: 35197292 Free PMC article.

6

Mice with a D190N mutation in the gene encoding rhodopsin: a model for human autosomal-dominant retinitis pigmentosa.

Sancho-Pelluz J, Tosi J, Hsu CW, Lee F, Wolpert K, Tabacaru MR, Greenberg JP, Tsang SH, Lin CS. Sancho-Pelluz J, et al. Among authors: lin cs. Mol Med. 2012 May 9;18(1):549-55. doi: 10.2119/molmed.2011.00475. Mol Med. 2012. PMID: 22252712 Free PMC article.

7

Reprogramming towards anabolism impedes degeneration in a preclinical model of retinitis pigmentosa.

Zhang L, Justus S, Xu Y, Pluchenik T, Hsu CW, Yang J, Duong JK, Lin CS, Jia Y, Bassuk AG, Mahajan VB, Tsang SH. Zhang L, et al. Among authors: lin cs. Hum Mol Genet. 2016 Oct 1;25(19):4244-4255. doi: 10.1093/hmg/ddw256. Epub 2016 Aug 11. Hum Mol Genet. 2016. PMID: 27516389 Free PMC article.

8

Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho^D190N mutation.

Sancho-Pelluz J, Cui X, Lee W, Tsai YT, Wu WH, Justus S, Washington I, Hsu CW, Park KS, Koch S, Velez G, Bassuk AG, Mahajan VB, Lin CS, Tsang SH. Sancho-Pelluz J, et al. Among authors: lin cs. Cell Mol Life Sci. 2019 Sep;76(18):3657-3665. doi: 10.1007/s00018-019-03090-9. Epub 2019 Apr 11. Cell Mol Life Sci. 2019. PMID: 30976840 Free PMC article.

9

Long-term vitamin A supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa.

Cui X, Kim HJ, Cheng CH, Jenny LA, Lima de Carvalho JR, Chang YJ, Kong Y, Hsu CW, Huang IW, Ragi SD, Lin CS, Li X, Sparrow JR, Tsang SH. Cui X, et al. Among authors: lin cs. Hum Mol Genet. 2022 Jul 21;31(14):2438-2451. doi: 10.1093/hmg/ddac032. Hum Mol Genet. 2022. PMID: 35195241 Free PMC article.

10

The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes.

Antoku S, Joseph LC, Dabhade P, Zhang BX, Lin CS, Schwartz TU, Kushner J, Fine BM, Morrow JP, Worman HJ, Gundersen GG. Antoku S, et al. Among authors: lin cs. bioRxiv [Preprint]. 2025 Jun 15:2025.06.13.659598. doi: 10.1101/2025.06.13.659598. bioRxiv. 2025. PMID: 40661556 Free PMC article. Preprint.

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