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Items: 1 to 20 of 87

1.
LncRNAs in the Dlk1-Dio3 Domain Are Essential for Mid-Embryonic Heart Development
Xiangqi Teng, Hongjuan He, Haoran Yu, Ximeijia Zhang, Jie Xing, Jiwei Shen, Chenghao Li, Mengyun Wang, Lan Shao, Ziwen Wang, Haopeng Yang, Yan Zhang, Qiong Wu
Int J Mol Sci. 2024 Aug; 25(15): 8184. Published online 2024 Jul 26. doi: 10.3390/ijms25158184
PMCID:
PMC11311489
AbstractArticlePDF–3.1M
2.
Transgenerational epigenetic self-memory of Dio3 dosage is associated with Meg3 methylation and altered growth trajectories and neonatal hormones
M. Elena Martinez, Aldona Karaczyn, Zhaofei Wu, Christian A. Bennett, Kassey L. Matoin, Heather M. Daigle, Arturo Hernandez
Epigenetics. 2024; 19(1): 2376948. Published online 2024 Jul 11. doi: 10.1080/15592294.2024.2376948
PMCID:
PMC11244338
AbstractArticlePDF–7.0M
3.
Mice lacking DIO3 exhibit sex-specific alterations in circadian patterns of corticosterone and gene expression in metabolic tissues
Zhaofei Wu, M. Elena Martinez, Arturo Hernandez
BMC Mol Cell Biol. 2024; 25: 11. Published online 2024 Mar 29. doi: 10.1186/s12860-024-00508-6
PMCID:
PMC10979634
AbstractArticlePDF–7.8M
4.
Maternal RNA transcription in Dlk1-Dio3 domain is critical for proper development of the mouse placental vasculature
Ximeijia Zhang, Hongjuan He, Haoran Yu, Xiangqi Teng, Ziwen Wang, Chenghao Li, Jiahang Li, Haopeng Yang, Jiwei Shen, Tong Wu, Fengwei Zhang, Yan Zhang, Qiong Wu
Commun Biol. 2024; 7: 363. Published online 2024 Mar 23. doi: 10.1038/s42003-024-06038-3
PMCID:
PMC10960817
AbstractArticlePDF–3.1M
5.
Paternal developmental thyrotoxicosis disrupts neonatal leptin leading to increased adiposity and altered physiology of the melanocortin system
Maria Elena Martinez, Zhaofei Wu, Arturo Hernandez
Front Endocrinol (Lausanne) 2023; 14: 1210414. Published online 2023 Jul 25. doi: 10.3389/fendo.2023.1210414
PMCID:
PMC10407661
AbstractArticlePDF–9.4M
6.
Meg8-DMR as the Secondary Regulatory Region Regulates the Expression of MicroRNAs While It Does Not Affect Embryonic Development in Mice
Liang Zhang, Zhengbin Han, Hongjuan He, Ximeijia Zhang, Mengyan Zhang, Boran Li, Qiong Wu
Genes (Basel) 2023 Jun; 14(6): 1264. Published online 2023 Jun 14. doi: 10.3390/genes14061264
PMCID:
PMC10298023
AbstractArticlePDF–4.2M
7.
USP7 represses lineage differentiation genes in mouse embryonic stem cells by both catalytic and noncatalytic activities
Chao Liu, Lingang Sun, Yijun Tan, Qi Wang, Tao Luo, Chenlu Li, Nan Yao, Yuting Xie, Xiao Yi, Yi Zhu, Tiannan Guo, Junfeng Ji
Sci Adv. 2023 May; 9(20): eade3888. Published online 2023 May 17. doi: 10.1126/sciadv.ade3888
PMCID:
PMC10191441
AbstractArticlePDF–2.4M
8.
Developmental thyroid hormone action on pro-opiomelanocortin-expressing cells programs hypothalamic BMPR1A depletion and brown fat activation
Zhaofei Wu, M Elena Martinez, Victoria DeMambro, Marie Francois, Arturo Hernandez
J Mol Cell Biol. 2022 Sep; 14(9): mjac078. Published online 2022 Dec 29. doi: 10.1093/jmcb/mjac078
PMCID:
PMC9982511
AbstractArticlePDF–5.4M
9.
Thyroid hormone elicits intergenerational epigenetic effects on adult social behavior and fetal brain expression of autism susceptibility genes
Maria Elena Martinez, Julia Patrizia Stohn, Elizabeth M. Mutina, Rayne J. Whitten, Arturo Hernandez
Front Neurosci. 2022; 16: 1055116. Published online 2022 Nov 7. doi: 10.3389/fnins.2022.1055116
PMCID:
PMC9676973
AbstractArticlePDF–2.1M
10.
DIO3 protects against thyrotoxicosis-derived cranio-encephalic and cardiac congenital abnormalities
M. Elena Martinez, Ilka Pinz, Marilena Preda, Christine R. Norton, Thomas Gridley, Arturo Hernandez
JCI Insight. 2022 Nov 8; 7(21): e161214. Published online 2022 Nov 8. doi: 10.1172/jci.insight.161214
PMCID:
PMC9675556
AbstractArticlePDF–3.9M
11.
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy
Ai Vu Hong, Nathalie Bourg, Peggy Sanatine, Jerome Poupiot, Karine Charton, Evelyne Gicquel, Emmanuelle Massourides, Marco Spinazzi, Isabelle Richard, David Israeli
Life Sci Alliance. 2023 Jan; 6(1): e202201506. Published online 2022 Oct 20. doi: 10.26508/lsa.202201506
PMCID:
PMC9585966
AbstractArticlePDF–3.1M
12.
Inactivation of Type 3 Deiodinase Results in Life-long Changes in the Brown Adipose Tissue Transcriptome in the Male Mouse
Tatiana L Fonseca, Samuel C Russo, Cristina Luongo, Domenico Salvatore, Antonio C Bianco
Endocrinology. 2022 May; 163(5): bqac026. Published online 2022 Mar 3. doi: 10.1210/endocr/bqac026
PMCID:
PMC8988869
AbstractArticle
13.
DNA methylation in the pathophysiology of hyperphenylalaninemia in the PAHenu2 mouse model of phenylketonuria
S.F. Dobrowolski, J. Lyons-Weiler, K. Spridik, J. Vockley, K. Skvorak, A. Biery
Mol Genet Metab. Author manuscript; available in PMC 2022 Mar 28.
Published in final edited form as: Mol Genet Metab. 2016 Sep; 119(1-2): 1–7. Published online 2016 Jan 14. doi: 10.1016/j.ymgme.2016.01.001
PMCID:
PMC8958364
AbstractArticlePDF–346K
14.
Spermatogonial Dio3 as a potential germ line sensor for thyroid hormone-driven epigenetic inheritance
Arturo Hernandez
Biol Reprod. 2021 Sep; 105(3): 613–615. Published online 2021 May 7. doi: 10.1093/biolre/ioab089
PMCID:
PMC8444671
AbstractArticlePDF–210K
15.
The Type 3 Deiodinase Is a Critical Modulator of Thyroid Hormone Sensitivity in the Fetal Brain
Maria Elena Martinez, Arturo Hernandez
Front Neurosci. 2021; 15: 703730. Published online 2021 Jun 29. doi: 10.3389/fnins.2021.703730
PMCID:
PMC8265566
AbstractArticlePDF–8.3M
16.
Humanization of a tandem repeat in IG-DMR causes stochastic restoration of paternal imprinting at mouse Dlk1-Dio3 domain
Satoshi Hara, Miho Terao, Atsumi Tsuji-Hosokawa, Yuya Ogawa, Shuji Takada
Hum Mol Genet. 2021 Apr 1; 30(7): 564–574. Published online 2021 Mar 11. doi: 10.1093/hmg/ddab071
PMCID:
PMC8120134
AbstractArticlePDF–1.6M
17.
Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes
Moe Kitazawa, Shinichiro Hayashi, Michihiro Imamura, Shin'ichi Takeda, Yumiko Oishi, Tomoko Kaneko-Ishino, Fumitoshi Ishino
Development. 2020 Nov 1; 147(21): dev185918. Published online 2020 Sep 3. doi: 10.1242/dev.185918
PMCID:
PMC7490516
AbstractArticle
18.
Adult onset of type 3 deiodinase deficiency in mice alters brain gene expression and increases locomotor activity
J. Patrizia Stohn, M. Elena Martinez, Donald L. St. Germain, Arturo Hernandez
Psychoneuroendocrinology. Author manuscript; available in PMC 2020 Dec 1.
Published in final edited form as: Psychoneuroendocrinology. 2019 Dec; 110: 104439. Published online 2019 Sep 18. doi: 10.1016/j.psyneuen.2019.104439
PMCID:
PMC7259167
AbstractArticlePDF–1.8M
19.
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Gayle B. Collin, Navdeep Gogna, Bo Chang, Nattaya Damkham, Jai Pinkney, Lillian F. Hyde, Lisa Stone, Jürgen K. Naggert, Patsy M. Nishina, Mark P. Krebs
Cells. 2020 Apr; 9(4): 931. Published online 2020 Apr 10. doi: 10.3390/cells9040931
PMCID:
PMC7227028
AbstractArticlePDF–5.4M
20.
Loss of TSC complex enhances gluconeogenesis via upregulation of Dlk1-Dio3 locus miRNAs
Dritan Liko, Andrzej Rzepiela, Vanja Vukojevic, Mihaela Zavolan, Michael N. Hall
Proc Natl Acad Sci U S A. 2020 Jan 21; 117(3): 1524–1532. Published online 2020 Jan 9. doi: 10.1073/pnas.1918931117
PMCID:
PMC6983401
AbstractArticlePDF–1.2M

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