PubMed for id: 306526240

Year	Number of Results
1999	1
2000	1
2003	1
2004	2
2005	1
2006	1
2007	2
2008	2
2009	2
2010	1
2011	4
2012	4
2013	2
2014	4
2016	1
2017	1
2018	1
2024	0

1

SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility.

Günther C, Lee-Kirsch MA, Eckhard J, Matanovic A, Kerscher T, Rüschendorf F, Klein B, Berndt N, Zimmermann N, Flachmeier C, Thuß T, Lucas N, Marenholz I, Esparza-Gordillo J, Hübner N, Traupe H, Delaporte E, Lee YA. Günther C, et al. J Invest Dermatol. 2018 Jun;138(6):1428-1431. doi: 10.1016/j.jid.2018.01.015. Epub 2018 Feb 1. J Invest Dermatol. 2018. PMID: 29409814 Free article. No abstract available.

2

Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation.

Hendriks IA, Lyon D, Young C, Jensen LJ, Vertegaal AC, Nielsen ML. Hendriks IA, et al. Nat Struct Mol Biol. 2017 Mar;24(3):325-336. doi: 10.1038/nsmb.3366. Epub 2017 Jan 23. Nat Struct Mol Biol. 2017. PMID: 28112733

3

Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Li M, Wang J, Li Z, Zhang J, Ni C, Cheng R, Yao Z. Li M, et al. Eur J Hum Genet. 2016 Aug;24(9):1367-70. doi: 10.1038/ejhg.2016.15. Epub 2016 Mar 2. Eur J Hum Genet. 2016. PMID: 26932190 Free PMC article.

4

Uncovering global SUMOylation signaling networks in a site-specific manner.

Hendriks IA, D'Souza RC, Yang B, Verlaan-de Vries M, Mann M, Vertegaal AC. Hendriks IA, et al. Nat Struct Mol Biol. 2014 Oct;21(10):927-36. doi: 10.1038/nsmb.2890. Epub 2014 Sep 14. Nat Struct Mol Biol. 2014. PMID: 25218447 Free PMC article.

5

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.

Nousbeck J, Sarig O, Magal L, Warshauer E, Burger B, Itin P, Sprecher E. Nousbeck J, et al. Br J Dermatol. 2014 Dec;171(6):1521-4. doi: 10.1111/bjd.13176. Epub 2014 Oct 26. Br J Dermatol. 2014. PMID: 24909267

6

Analysis of two candidate genes for Basan syndrome.

Marks KC, Banks WR 3rd, Cunningham D, Witman PM, Herman GE. Marks KC, et al. Am J Med Genet A. 2014 May;164A(5):1188-91. doi: 10.1002/ajmg.a.36438. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24664640

7

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

Bian Y, Song C, Cheng K, Dong M, Wang F, Huang J, Sun D, Wang L, Ye M, Zou H. Bian Y, et al. J Proteomics. 2014 Jan 16;96:253-62. doi: 10.1016/j.jprot.2013.11.014. Epub 2013 Nov 22. J Proteomics. 2014. PMID: 24275569 Clinical Trial.

8

Toward a comprehensive characterization of a human cancer cell phosphoproteome.

Zhou H, Di Palma S, Preisinger C, Peng M, Polat AN, Heck AJ, Mohammed S. Zhou H, et al. J Proteome Res. 2013 Jan 4;12(1):260-71. doi: 10.1021/pr300630k. Epub 2012 Dec 18. J Proteome Res. 2013. PMID: 23186163

9

The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection.

Costelloe T, Louge R, Tomimatsu N, Mukherjee B, Martini E, Khadaroo B, Dubois K, Wiegant WW, Thierry A, Burma S, van Attikum H, Llorente B. Costelloe T, et al. Nature. 2012 Sep 27;489(7417):581-4. doi: 10.1038/nature11353. Epub 2012 Sep 9. Nature. 2012. PMID: 22960744 Free PMC article.

10

N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

Van Damme P, Lasa M, Polevoda B, Gazquez C, Elosegui-Artola A, Kim DS, De Juan-Pardo E, Demeyer K, Hole K, Larrea E, Timmerman E, Prieto J, Arnesen T, Sherman F, Gevaert K, Aldabe R. Van Damme P, et al. Proc Natl Acad Sci U S A. 2012 Jul 31;109(31):12449-54. doi: 10.1073/pnas.1210303109. Epub 2012 Jul 18. Proc Natl Acad Sci U S A. 2012. PMID: 22814378 Free PMC article.

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