Anastassiadis K - Search Results

1

MLL4 is required after implantation, whereas MLL3 becomes essential during late gestation.

Ashokkumar D, Zhang Q, Much C, Bledau AS, Naumann R, Alexopoulou D, Dahl A, Goveas N, Fu J, Anastassiadis K, Stewart AF, Kranz A. Ashokkumar D, et al. Among authors: anastassiadis k. Development. 2020 Jun 17;147(12):dev186999. doi: 10.1242/dev.186999. Development. 2020. PMID: 32439762

2

The H3K4 methyltransferase Setd1a is first required at the epiblast stage, whereas Setd1b becomes essential after gastrulation.

Bledau AS, Schmidt K, Neumann K, Hill U, Ciotta G, Gupta A, Torres DC, Fu J, Kranz A, Stewart AF, Anastassiadis K. Bledau AS, et al. Among authors: anastassiadis k. Development. 2014 Mar;141(5):1022-35. doi: 10.1242/dev.098152. Development. 2014. PMID: 24550110

3

Setd1b, encoding a histone 3 lysine 4 methyltransferase, is a maternal effect gene required for the oogenic gene expression program.

Brici D, Zhang Q, Reinhardt S, Dahl A, Hartmann H, Schmidt K, Goveas N, Huang J, Gahurova L, Kelsey G, Anastassiadis K, Stewart AF, Kranz A. Brici D, et al. Among authors: anastassiadis k. Development. 2017 Jul 15;144(14):2606-2617. doi: 10.1242/dev.143347. Epub 2017 Jun 15. Development. 2017. PMID: 28619824

4

MLL1 is required for maintenance of intestinal stem cells.

Goveas N, Waskow C, Arndt K, Heuberger J, Zhang Q, Alexopoulou D, Dahl A, Birchmeier W, Anastassiadis K, Stewart AF, Kranz A. Goveas N, et al. Among authors: anastassiadis k. PLoS Genet. 2021 Dec 3;17(12):e1009250. doi: 10.1371/journal.pgen.1009250. eCollection 2021 Dec. PLoS Genet. 2021. PMID: 34860830 Free PMC article.

5

Kmt2b conveys monovalent and bivalent H3K4me3 in mouse spermatogonial stem cells at germline and embryonic promoters.

Tomizawa SI, Kobayashi Y, Shirakawa T, Watanabe K, Mizoguchi K, Hoshi I, Nakajima K, Nakabayashi J, Singh S, Dahl A, Alexopoulou D, Seki M, Suzuki Y, Royo H, Peters AHFM, Anastassiadis K, Stewart AF, Ohbo K. Tomizawa SI, et al. Among authors: anastassiadis k. Development. 2018 Nov 30;145(23):dev169102. doi: 10.1242/dev.169102. Development. 2018. PMID: 30504434

6

The role of SETD1A and SETD1B in development and disease.

Kranz A, Anastassiadis K. Kranz A, et al. Among authors: anastassiadis k. Biochim Biophys Acta Gene Regul Mech. 2020 Aug;1863(8):194578. doi: 10.1016/j.bbagrm.2020.194578. Epub 2020 May 8. Biochim Biophys Acta Gene Regul Mech. 2020. PMID: 32389824 Review.

7

[No title available]

[No authors listed] [No authors listed] PMID: 34004928

8

Multiple epigenetic maintenance factors implicated by the loss of Mll2 in mouse development.

Glaser S, Schaft J, Lubitz S, Vintersten K, van der Hoeven F, Tufteland KR, Aasland R, Anastassiadis K, Ang SL, Stewart AF. Glaser S, et al. Among authors: anastassiadis k. Development. 2006 Apr;133(8):1423-32. doi: 10.1242/dev.02302. Epub 2006 Mar 15. Development. 2006. PMID: 16540515

9

An improved Flp deleter mouse in C57Bl/6 based on Flpo recombinase.

Kranz A, Fu J, Duerschke K, Weidlich S, Naumann R, Stewart AF, Anastassiadis K. Kranz A, et al. Among authors: anastassiadis k. Genesis. 2010 Aug;48(8):512-20. doi: 10.1002/dvg.20641. Genesis. 2010. PMID: 20506501

10

Mll2 is required for H3K4 trimethylation on bivalent promoters in embryonic stem cells, whereas Mll1 is redundant.

Denissov S, Hofemeister H, Marks H, Kranz A, Ciotta G, Singh S, Anastassiadis K, Stunnenberg HG, Stewart AF. Denissov S, et al. Among authors: anastassiadis k. Development. 2014 Feb;141(3):526-37. doi: 10.1242/dev.102681. Epub 2014 Jan 14. Development. 2014. PMID: 24423662

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