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Items: 9

1.

Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes.

Loi M, Cenni V, Duchi S, Squarzoni S, Lopez-Otin C, Foisner R, Lattanzi G, Capanni C.

Oncotarget. 2016 Mar 29;7(13):15662-77. doi: 10.18632/oncotarget.6697.

2.

NF-κB activation impairs somatic cell reprogramming in ageing.

Soria-Valles C, Osorio FG, Gutiérrez-Fernández A, De Los Angeles A, Bueno C, Menéndez P, Martín-Subero JI, Daley GQ, Freije JM, López-Otín C.

Nat Cell Biol. 2015 Aug;17(8):1004-13. doi: 10.1038/ncb3207. Epub 2015 Jul 27.

PMID:
26214134
3.

Néstor-Guillermo Progeria Syndrome: a biochemical insight into Barrier-to-Autointegration Factor 1, alanine 12 threonine mutation.

Paquet N, Box JK, Ashton NW, Suraweera A, Croft LV, Urquhart AJ, Bolderson E, Zhang SD, O'Byrne KJ, Richard DJ.

BMC Mol Biol. 2014 Dec 12;15:27. doi: 10.1186/s12867-014-0027-z.

4.

The molecular basis of emerin-emerin and emerin-BAF interactions.

Berk JM, Simon DN, Jenkins-Houk CR, Westerbeck JW, Grønning-Wang LM, Carlson CR, Wilson KL.

J Cell Sci. 2014 Sep 15;127(Pt 18):3956-69. doi: 10.1242/jcs.148247. Epub 2014 Jul 22.

5.

The nuclear envelope LEM-domain protein emerin.

Berk JM, Tifft KE, Wilson KL.

Nucleus. 2013 Jul-Aug;4(4):298-314. doi: 10.4161/nucl.25751. Epub 2013 Jul 17. Review.

6.

Possible roles of barrier-to-autointegration factor 1 in regulation of keratinocyte differentiation and proliferation.

Takama H, Sugiura K, Ogawa Y, Muro Y, Akiyama M.

J Dermatol Sci. 2013 Aug;71(2):100-6. doi: 10.1016/j.jdermsci.2013.04.007. Epub 2013 Apr 19.

PMID:
23664529
7.

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A.

Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18.

PMID:
22991222
8.

Cell autonomous and systemic factors in progeria development.

Osorio FG, Ugalde AP, Mariño G, Puente XS, Freije JM, López-Otín C.

Biochem Soc Trans. 2011 Dec;39(6):1710-4. doi: 10.1042/BST20110677. Review.

PMID:
22103512
9.

Néstor-Guillermo progeria syndrome: a novel premature aging condition with early onset and chronic development caused by BANF1 mutations.

Cabanillas R, Cadiñanos J, Villameytide JA, Pérez M, Longo J, Richard JM, Alvarez R, Durán NS, Illán R, González DJ, López-Otín C.

Am J Med Genet A. 2011 Nov;155A(11):2617-25. doi: 10.1002/ajmg.a.34249. Epub 2011 Sep 19.

PMID:
21932319

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