Wang Y - Search Results

1

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.

Wang Y, Herron AJ, Worman HJ. Wang Y, et al. Hum Mol Genet. 2006 Aug 15;15(16):2479-89. doi: 10.1093/hmg/ddl170. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825283

2

Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin.

Wang Y, Panteleyev AA, Owens DM, Djabali K, Stewart CL, Worman HJ. Wang Y, et al. Hum Mol Genet. 2008 Aug 1;17(15):2357-69. doi: 10.1093/hmg/ddn136. Epub 2008 Apr 28. Hum Mol Genet. 2008. PMID: 18442998 Free PMC article.

3

Diseases of the nuclear envelope.

Worman HJ, Ostlund C, Wang Y. Worman HJ, et al. Among authors: wang y. Cold Spring Harb Perspect Biol. 2010 Feb;2(2):a000760. doi: 10.1101/cshperspect.a000760. Cold Spring Harb Perspect Biol. 2010. PMID: 20182615 Free PMC article. Review.

4

Blocking protein farnesylation improves nuclear shape abnormalities in keratinocytes of mice expressing the prelamin A variant in Hutchinson-Gilford progeria syndrome.

Wang Y, Ostlund C, Worman HJ. Wang Y, et al. Nucleus. 2010 Sep-Oct;1(5):432-9. doi: 10.4161/nucl.1.5.12972. Nucleus. 2010. PMID: 21326826 Free PMC article.

5

Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance.

Shin JY, Méndez-López I, Wang Y, Hays AP, Tanji K, Lefkowitch JH, Schulze PC, Worman HJ, Dauer WT. Shin JY, et al. Among authors: wang y. Dev Cell. 2013 Sep 30;26(6):591-603. doi: 10.1016/j.devcel.2013.08.012. Epub 2013 Sep 19. Dev Cell. 2013. PMID: 24055652 Free PMC article.

6

Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth.

Shin JY, Méndez-López I, Hong M, Wang Y, Tanji K, Wu W, Shugol L, Krauss RS, Dauer WT, Worman HJ. Shin JY, et al. Among authors: wang y. Hum Mol Genet. 2017 Jan 1;26(1):65-78. doi: 10.1093/hmg/ddw368. Hum Mol Genet. 2017. PMID: 27798115 Free PMC article.

7

Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1.

Wang Y, Shin JY, Nakanishi K, Homma S, Kim GJ, Tanji K, Joseph LC, Morrow JP, Stewart CL, Dauer WT, Worman HJ. Wang Y, et al. Hum Mol Genet. 2019 Aug 1;28(15):2486-2500. doi: 10.1093/hmg/ddz082. Hum Mol Genet. 2019. PMID: 31009944 Free PMC article.

8

Blocking farnesylation of the prelamin A variant in Hutchinson-Gilford progeria syndrome alters the distribution of A-type lamins.

Wang Y, Ostlund C, Choi JC, Swayne TC, Gundersen GG, Worman HJ. Wang Y, et al. Nucleus. 2012 Sep-Oct;3(5):452-62. doi: 10.4161/nucl.21675. Epub 2012 Aug 16. Nucleus. 2012. PMID: 22895092 Free PMC article.

9

Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- mice.

Frock RL, Chen SC, Da DF, Frett E, Lau C, Brown C, Pak DN, Wang Y, Muchir A, Worman HJ, Santana LF, Ladiges WC, Rabinovitch PS, Kennedy BK. Frock RL, et al. Among authors: wang y. PLoS One. 2012;7(8):e42918. doi: 10.1371/journal.pone.0042918. Epub 2012 Aug 15. PLoS One. 2012. PMID: 22905185 Free PMC article.

10

A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder.

Wang Y, Lichter-Konecki U, Anyane-Yeboa K, Shaw JE, Lu JT, Östlund C, Shin JY, Clark LN, Gundersen GG, Nagy PL, Worman HJ. Wang Y, et al. J Cell Sci. 2016 May 15;129(10):1975-80. doi: 10.1242/jcs.187302. Epub 2016 Mar 31. J Cell Sci. 2016. PMID: 27034136 Free PMC article.

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