Kozlov S - Search Results

1

Nesprin-1 LINC complexes recruit microtubule cytoskeleton proteins and drive pathology in Lmna-mutant striated muscle.

Leong EL, Khaing NT, Cadot B, Hong WL, Kozlov S, Werner H, Wong ESM, Stewart CL, Burke B, Lee YL. Leong EL, et al. Among authors: kozlov s. Hum Mol Genet. 2023 Jan 6;32(2):177-191. doi: 10.1093/hmg/ddac179. Hum Mol Genet. 2023. PMID: 35925868 Free PMC article.

2

Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

Mounkes LC, Kozlov SV, Rottman JN, Stewart CL. Mounkes LC, et al. Hum Mol Genet. 2005 Aug 1;14(15):2167-80. doi: 10.1093/hmg/ddi221. Epub 2005 Jun 22. Hum Mol Genet. 2005. PMID: 15972724

3

The laminopathies: nuclear structure meets disease.

Mounkes L, Kozlov S, Burke B, Stewart CL. Mounkes L, et al. Among authors: kozlov s. Curr Opin Genet Dev. 2003 Jun;13(3):223-30. doi: 10.1016/s0959-437x(03)00058-3. Curr Opin Genet Dev. 2003. PMID: 12787783 Review.

4

The LINC complex is essential for hearing.

Horn HF, Brownstein Z, Lenz DR, Shivatzki S, Dror AA, Dagan-Rosenfeld O, Friedman LM, Roux KJ, Kozlov S, Jeang KT, Frydman M, Burke B, Stewart CL, Avraham KB. Horn HF, et al. Among authors: kozlov s. J Clin Invest. 2013 Feb;123(2):740-50. doi: 10.1172/JCI66911. Epub 2013 Jan 25. J Clin Invest. 2013. PMID: 23348741 Free PMC article.

5

Tissue specific loss of A-type lamins in the gastrointestinal epithelium can enhance polyp size.

Wang AS, Kozlov SV, Stewart CL, Horn HF. Wang AS, et al. Among authors: kozlov sv. Differentiation. 2015 Jan-Feb;89(1-2):11-21. doi: 10.1016/j.diff.2014.12.002. Epub 2015 Jan 8. Differentiation. 2015. PMID: 25578479

6

Nesprin 4 is an outer nuclear membrane protein that can induce kinesin-mediated cell polarization.

Roux KJ, Crisp ML, Liu Q, Kim D, Kozlov S, Stewart CL, Burke B. Roux KJ, et al. Among authors: kozlov s. Proc Natl Acad Sci U S A. 2009 Feb 17;106(7):2194-9. doi: 10.1073/pnas.0808602106. Epub 2009 Jan 21. Proc Natl Acad Sci U S A. 2009. PMID: 19164528 Free PMC article.

7

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N. De Sandre-Giovannoli A, et al. Among authors: kozlov s. Am J Hum Genet. 2002 Mar;70(3):726-36. doi: 10.1086/339274. Epub 2002 Jan 17. Am J Hum Genet. 2002. PMID: 11799477 Free PMC article.

8

A progeroid syndrome in mice is caused by defects in A-type lamins.

Mounkes LC, Kozlov S, Hernandez L, Sullivan T, Stewart CL. Mounkes LC, et al. Among authors: kozlov s. Nature. 2003 May 15;423(6937):298-301. doi: 10.1038/nature01631. Nature. 2003. PMID: 12748643

9

Mutations in the mouse Lmna gene causing progeria, muscular dystrophy and cardiomyopathy.

Kozlov S, Mounkes L, Cutler D, Sullivan T, Hernandez L, Levy N, Rottman J, Stewart CL. Kozlov S, et al. Novartis Found Symp. 2005;264:246-58; discussion 258-63. Novartis Found Symp. 2005. PMID: 15773758 Review.

10

Mouse models of the laminopathies.

Stewart CL, Kozlov S, Fong LG, Young SG. Stewart CL, et al. Among authors: kozlov s. Exp Cell Res. 2007 Jun 10;313(10):2144-56. doi: 10.1016/j.yexcr.2007.03.026. Epub 2007 Mar 31. Exp Cell Res. 2007. PMID: 17493612 Free PMC article. Review.

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