398 related articles for article (PubMed ID: 29716999)
1. The histone methyltransferase SETD2 is required for expression of acrosin-binding protein 1 and protamines and essential for spermiogenesis in mice.
Zuo X; Rong B; Li L; Lv R; Lan F; Tong MH
J Biol Chem; 2018 Jun; 293(24):9188-9197. PubMed ID: 29716999
[TBL] [Abstract][Full Text] [Related]
2. MRG15 is required for pre-mRNA splicing and spermatogenesis.
Iwamori N; Tominaga K; Sato T; Riehle K; Iwamori T; Ohkawa Y; Coarfa C; Ono E; Matzuk MM
Proc Natl Acad Sci U S A; 2016 Sep; 113(37):E5408-15. PubMed ID: 27573846
[TBL] [Abstract][Full Text] [Related]
3. The Benzene Hematotoxic and Reactive Metabolite 1,4-Benzoquinone Impairs the Activity of the Histone Methyltransferase SET Domain Containing 2 (SETD2) and Causes Aberrant Histone H3 Lysine 36 Trimethylation (H3K36me3).
Berthelet J; Michail C; Bui LC; Le Coadou L; Sirri V; Wang L; Dulphy N; Dupret JM; Chomienne C; Guidez F; Rodrigues-Lima F
Mol Pharmacol; 2021 Sep; 100(3):283-294. PubMed ID: 34266924
[TBL] [Abstract][Full Text] [Related]
4. PHF7 is a novel histone H2A E3 ligase prior to histone-to-protamine exchange during spermiogenesis.
Wang X; Kang JY; Wei L; Yang X; Sun H; Yang S; Lu L; Yan M; Bai M; Chen Y; Long J; Li N; Li D; Huang J; Lei M; Shao Z; Yuan W; Zuo E; Lu K; Liu MF; Li J
Development; 2019 Jul; 146(13):. PubMed ID: 31189663
[TBL] [Abstract][Full Text] [Related]
5. Tsga8 is required for spermatid morphogenesis and male fertility in mice.
Kobayashi Y; Tomizawa SI; Ono M; Kuroha K; Minamizawa K; Natsume K; Dizdarević S; Dočkal I; Tanaka H; Kawagoe T; Seki M; Suzuki Y; Ogonuki N; Inoue K; Matoba S; Anastassiadis K; Mizuki N; Ogura A; Ohbo K
Development; 2021 Apr; 148(8):. PubMed ID: 33766931
[TBL] [Abstract][Full Text] [Related]
6. DOT1L promotes spermatid differentiation by regulating expression of genes required for histone-to-protamine replacement.
Malla AB; Rainsford SR; Smith ZD; Lesch BJ
Development; 2023 May; 150(9):. PubMed ID: 37082969
[TBL] [Abstract][Full Text] [Related]
7. Testis-expressed protein 33 is not essential for spermiogenesis and fertility in mice.
Xia M; Xia J; Niu C; Zhong Y; Ge T; Ding Y; Zheng Y
Mol Med Rep; 2021 May; 23(5):. PubMed ID: 33760102
[TBL] [Abstract][Full Text] [Related]
8. TSSK6 is required for γH2AX formation and the histone-to-protamine transition during spermiogenesis.
Jha KN; Tripurani SK; Johnson GR
J Cell Sci; 2017 May; 130(10):1835-1844. PubMed ID: 28389581
[TBL] [Abstract][Full Text] [Related]
9. BAF-L Modulates Histone-to-Protamine Transition during Spermiogenesis.
Huang C; Gong H; Mu B; Lan X; Yang C; Tan J; Liu W; Zou Y; Li L; Feng B; He X; Luo Q; Chen Z
Int J Mol Sci; 2022 Feb; 23(4):. PubMed ID: 35216101
[TBL] [Abstract][Full Text] [Related]
10. ZFP628 Is a TAF4b-Interacting Transcription Factor Required for Mouse Spermiogenesis.
Gustafson EA; Seymour KA; Sigrist K; Rooij DGDE; Freiman RN
Mol Cell Biol; 2020 Mar; 40(7):. PubMed ID: 31932482
[TBL] [Abstract][Full Text] [Related]
11. H3K36me2 methyltransferase NSD2 orchestrates epigenetic reprogramming during spermatogenesis.
Li Z; Zhang X; Xie S; Liu X; Fei C; Huang X; Tang Y; Zhou LQ
Nucleic Acids Res; 2022 Jul; 50(12):6786-6800. PubMed ID: 35736136
[TBL] [Abstract][Full Text] [Related]
12. H3K36 trimethylation mediated by SETD2 regulates the fate of bone marrow mesenchymal stem cells.
Wang L; Niu N; Li L; Shao R; Ouyang H; Zou W
PLoS Biol; 2018 Nov; 16(11):e2006522. PubMed ID: 30422989
[TBL] [Abstract][Full Text] [Related]
13. Single-Cell Transcriptomic Profiling of the Mouse Testicular Germ Cells Reveals Important Role of Phosphorylated GRTH/DDX25 in Round Spermatid Differentiation and Acrosome Biogenesis during Spermiogenesis.
Kavarthapu R; Anbazhagan R; Pal S; Dufau ML
Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36834539
[TBL] [Abstract][Full Text] [Related]
14. Jmjd1a demethylase-regulated histone modification is essential for cAMP-response element modulator-regulated gene expression and spermatogenesis.
Liu Z; Zhou S; Liao L; Chen X; Meistrich M; Xu J
J Biol Chem; 2010 Jan; 285(4):2758-70. PubMed ID: 19910458
[TBL] [Abstract][Full Text] [Related]
15. SETD2 deficiency accelerates MDS-associated leukemogenesis via S100a9 in NHD13 mice and predicts poor prognosis in MDS.
Chen BY; Song J; Hu CL; Chen SB; Zhang Q; Xu CH; Wu JC; Hou D; Sun M; Zhang YL; Liu N; Yu PC; Liu P; Zong LJ; Zhang JY; Dai RF; Lan F; Huang QH; Zhang SJ; Nimer SD; Chen Z; Chen SJ; Sun XJ; Wang L
Blood; 2020 Jun; 135(25):2271-2285. PubMed ID: 32202636
[TBL] [Abstract][Full Text] [Related]
16. IP6K1 is essential for chromatoid body formation and temporal regulation of
Malla AB; Bhandari R
J Cell Sci; 2017 Sep; 130(17):2854-2866. PubMed ID: 28743739
[TBL] [Abstract][Full Text] [Related]
17. SETD2-dependent H3K36me3 plays a critical role in epigenetic regulation of the HPV31 life cycle.
Gautam D; Johnson BA; Mac M; Moody CA
PLoS Pathog; 2018 Oct; 14(10):e1007367. PubMed ID: 30312361
[TBL] [Abstract][Full Text] [Related]
18. Testis-specific miRNA-469 up-regulated in gonadotropin-regulated testicular RNA helicase (GRTH/DDX25)-null mice silences transition protein 2 and protamine 2 messages at sites within coding region: implications of its role in germ cell development.
Dai L; Tsai-Morris CH; Sato H; Villar J; Kang JH; Zhang J; Dufau ML
J Biol Chem; 2011 Dec; 286(52):44306-18. PubMed ID: 22086916
[TBL] [Abstract][Full Text] [Related]
19. Expression of protamine-1 and -2 mRNA during human spermiogenesis.
Steger K; Pauls K; Klonisch T; Franke FE; Bergmann M
Mol Hum Reprod; 2000 Mar; 6(3):219-25. PubMed ID: 10694268
[TBL] [Abstract][Full Text] [Related]
20. Deficiency in the omega-3 fatty acid pathway results in failure of acrosome biogenesis in mice.
Roqueta-Rivera M; Abbott TL; Sivaguru M; Hess RA; Nakamura MT
Biol Reprod; 2011 Oct; 85(4):721-32. PubMed ID: 21653892
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
