PubMed for id: 1677500629

Year	Number of Results
2000	2
2008	1
2011	3
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

Keeping chromatin quiet: how nucleosome remodeling restores heterochromatin after replication.

Mermoud JE, Rowbotham SP, Varga-Weisz PD. Mermoud JE, et al. Cell Cycle. 2011 Dec 1;10(23):4017-25. doi: 10.4161/cc.10.23.18558. Epub 2011 Dec 1. Cell Cycle. 2011. PMID: 22101266 Free PMC article. Review.

6

A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Nousbeck J, Burger B, Fuchs-Telem D, Pavlovsky M, Fenig S, Sarig O, Itin P, Sprecher E. Nousbeck J, et al. Am J Hum Genet. 2011 Aug 12;89(2):302-7. doi: 10.1016/j.ajhg.2011.07.004. Epub 2011 Aug 4. Am J Hum Genet. 2011. PMID: 21820097 Free PMC article.

7

Maintenance of silent chromatin through replication requires SWI/SNF-like chromatin remodeler SMARCAD1.

Rowbotham SP, Barki L, Neves-Costa A, Santos F, Dean W, Hawkes N, Choudhary P, Will WR, Webster J, Oxley D, Green CM, Varga-Weisz P, Mermoud JE. Rowbotham SP, et al. Mol Cell. 2011 May 6;42(3):285-96. doi: 10.1016/j.molcel.2011.02.036. Mol Cell. 2011. PMID: 21549307 Free article.

8

The novel protein complex with SMARCAD1/KIAA1122 binds to the vicinity of TSS.

Okazaki N, Ikeda S, Ohara R, Shimada K, Yanagawa T, Nagase T, Ohara O, Koga H. Okazaki N, et al. J Mol Biol. 2008 Oct 3;382(2):257-65. doi: 10.1016/j.jmb.2008.07.031. Epub 2008 Jul 17. J Mol Biol. 2008. PMID: 18675275

9

SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases.

Adra CN, Donato JL, Badovinac R, Syed F, Kheraj R, Cai H, Moran C, Kolker MT, Turner H, Weremowicz S, Shirakawa T, Morton CC, Schnipper LE, Drews R. Adra CN, et al. Genomics. 2000 Oct 15;69(2):162-73. doi: 10.1006/geno.2000.6281. Genomics. 2000. PMID: 11031099

10

A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.

Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A. Lee YA, et al. Am J Hum Genet. 2000 Jan;66(1):326-30. doi: 10.1086/302718. Am J Hum Genet. 2000. PMID: 10631162 Free PMC article. No abstract available.

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