PubMed (GeneRIF) for id: 56916

Year	Number of Results
2008	1
2011	2
2012	1
2014	1
2016	3
2017	1
2018	4
2019	2
2020	1
2021	1
2023	2
2024	1

1

Basan syndrome in a family from South India: a novel SMARCAD1 variant.

Mathews I, Wagh S, Baby A, Chandrashekar L, Dalal A. Mathews I, et al. Clin Exp Dermatol. 2024 Mar 21;49(4):437-440. doi: 10.1093/ced/llad393. Clin Exp Dermatol. 2024. PMID: 37966719 No abstract available.

2

The Conserved Chromatin Remodeler SMARCAD1 Interacts with TFIIIC and Architectural Proteins in Human and Mouse.

Sachs P, Bergmaier P, Treutwein K, Mermoud JE. Sachs P, et al. Genes (Basel). 2023 Sep 13;14(9):1793. doi: 10.3390/genes14091793. Genes (Basel). 2023. PMID: 37761933 Free PMC article.

3

MSH2-MSH3 promotes DNA end resection during homologous recombination and blocks polymerase theta-mediated end-joining through interaction with SMARCAD1 and EXO1.

Oh JM, Kang Y, Park J, Sung Y, Kim D, Seo Y, Lee EA, Ra JS, Amarsanaa E, Park YU, Lee SY, Hwang JM, Kim H, Schärer O, Cho SW, Lee C, Takata KI, Lee JY, Myung K. Oh JM, et al. Nucleic Acids Res. 2023 Jun 23;51(11):5584-5602. doi: 10.1093/nar/gkad308. Nucleic Acids Res. 2023. PMID: 37140056 Free PMC article.

4

Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1.

Loh AYT, Ho CM, Muthiah S, Venkatesh B, Zwolinski S, Bray APJJ, Reversade B, Rajan N, Carney TJ. Loh AYT, et al. Br J Dermatol. 2021 Jun;184(6):1205-1207. doi: 10.1111/bjd.19799. Epub 2021 Mar 10. Br J Dermatol. 2021. PMID: 33400266 No abstract available.

5

SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cells.

Takeishi Y, Fujikane R, Rikitake M, Obayashi Y, Sekiguchi M, Hidaka M. Takeishi Y, et al. J Biol Chem. 2020 Jan 24;295(4):1056-1065. doi: 10.1074/jbc.RA119.008854. Epub 2019 Dec 16. J Biol Chem. 2020. PMID: 31843968 Free PMC article.

6

A Ubiquitin-Binding Domain that Binds a Structural Fold Distinct from that of Ubiquitin.

Lim M, Newman JA, Williams HL, Masino L, Aitkenhead H, Gravard AE, Gileadi O, Svejstrup JQ. Lim M, et al. Structure. 2019 Aug 6;27(8):1316-1325.e6. doi: 10.1016/j.str.2019.05.003. Epub 2019 Jun 13. Structure. 2019. PMID: 31204252 Free PMC article.

7

SMARCAD1 in Breast Cancer Progression.

Arafat K, Al Kubaisy E, Sulaiman S, Karam SM, Al Natour Z, Hassan AH, Attoub S. Arafat K, et al. Cell Physiol Biochem. 2018;50(2):489-500. doi: 10.1159/000494163. Epub 2018 Oct 11. Cell Physiol Biochem. 2018. PMID: 30308496 Free article.

8

Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1.

Terui R, Nagao K, Kawasoe Y, Taki K, Higashi TL, Tanaka S, Nakagawa T, Obuse C, Masukata H, Takahashi TS. Terui R, et al. Genes Dev. 2018 Jun 1;32(11-12):806-821. doi: 10.1101/gad.310995.117. Epub 2018 Jun 13. Genes Dev. 2018. PMID: 29899141 Free PMC article.

9

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.

10

The CUE1 domain of the SNF2-like chromatin remodeler SMARCAD1 mediates its association with KRAB-associated protein 1 (KAP1) and KAP1 target genes.

Ding D, Bergmaier P, Sachs P, Klangwart M, Rückert T, Bartels N, Demmers J, Dekker M, Poot RA, Mermoud JE. Ding D, et al. J Biol Chem. 2018 Feb 23;293(8):2711-2724. doi: 10.1074/jbc.RA117.000959. Epub 2017 Dec 28. J Biol Chem. 2018. PMID: 29284678 Free PMC article.

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