Zobrazeno 1 - 10 of 356 pro vyhledávání: '"M, Rigolet"'
1
Akademický článek
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2
Akademický článek
Comparison of Autologous and Allogeneic Adipose-Derived Stem Cells in Kidney Transplantation: Immunological Considerations and Therapeutic Efficacy.
Autor: Fodor Duric, Ljiljana1 (AUTHOR) fodorlj@gmail.com, Basic Jukic, Nikolina2 (AUTHOR) nina_basic@net.hr, Vujicic, Bozidar3 (AUTHOR) vujicic.bozidar@gmail.com
Publikováno v: Journal of Clinical Medicine. Oct2024, Vol. 13 Issue 19, p5763. 18p.
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3
The epigenetic imprinting defect of patients with Beckwith--Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region
Autor: C Gicquel, Virginie Steunou, Antoine Kerjean, Céline Chalas, Pierre Jouannet, Y. Le Bouc, E Viegas-Pequignot, M Rigolet, Sylvie Rossignol
Publikováno v: Journal of Medical Genetics. 43:902-907
Background: Genomic imprinting refers to an epigenetic marking resulting in monoallelic gene expression and has a critical role in fetal development. Various imprinting diseases have recently been reported in humans and animals born after the use of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aeaa4a35ea95c75b60987975025acc5
https://doi.org/10.1136/jmg.2006.042135
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4
DNMT3B mutations and DNA methylation defect define two types of ICF syndrome
Autor: F Nigon, Anne Moncla, André Mégarbané, P. Maraschio, P Jonveaux, Déborah Bourc'his, Maj Hultén, Jean-Pierre Fryns, YL Jiang, M Rigolet, I Bokesoy, E Viegas-Pequignot
Publikováno v: Human Mutation. 25:56-63
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centromeric instability, and facial abnormalities. Mutations in the catalytic domain of DNMT3B, a gene encoding a de novo DNA methyltransferase, have been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6c5774065aaeed5dd5d394baffa67760
https://doi.org/10.1002/humu.20113
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5
Akademický článek
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6
Expression of Id2 and Id3 mRNA in human lymphocytes
Autor: M Rigolet, Akira Ishiguro, John D. Norton, Andreas Tobler, Toshikazu Shimbo, H. P. Koeffler, M Shiohara, K S Spirin
Publikováno v: Leukemia Research. 19:989-996
Helix-loop-helix (HLH) transcription factors are involved in cellular growth and differentiation. The Id (inhibitor of DNA binding and differentiation) HLH proteins, in a dominantly negative fashion, regulate transcriptional activities of basic HLH p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed53e8817db7191400623d9c199dbc4
https://doi.org/10.1016/0145-2126(95)00084-4
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7
Akademický článek
Adenosine diphosphate released from stressed cells triggers mitochondrial transfer to achieve tissue homeostasis.
Autor: Li, Hao1,2 (AUTHOR), Yu, Hongping3 (AUTHOR), Liu, Delin1,2 (AUTHOR), Liao, Peng1,2 (AUTHOR), Gao, Chuan1,2 (AUTHOR), Zhou, Jian1,2 (AUTHOR), Mei, Jialun1,2 (AUTHOR), Zong, Yao4,5 (AUTHOR), Ding, Peng1,2 (AUTHOR), Yao, Meng1,2 (AUTHOR), Wang, Bingqi1,2 (AUTHOR), Lu, Yafei1,2 (AUTHOR), Huang, Yigang1,2 (AUTHOR), Gao, Youshui1,2 (AUTHOR) gaoyoushui@sjtu.edu.cn, Zhang, Changqing1,2 (AUTHOR) zhangcq@sjtu.edu.cn, Zheng, Minghao4,5 (AUTHOR) minghao.zheng@uwa.edu.au, Gao, Junjie1,2 (AUTHOR) colingjj@163.com
Publikováno v: PLoS Biology. 8/20/2024, Vol. 22 Issue 8, p1-25. 25p.
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8
Akademický článek
ASM is a therapeutic target in dermatomyositis by regulating the differentiation of naive CD4 + T cells into Th17 and Treg subsets.
Autor: Chen, Yuehong1 (AUTHOR), Liu, Huan1 (AUTHOR), Luo, Zhongling1 (AUTHOR), Zhang, Jiaqian1 (AUTHOR), Dong, Min1 (AUTHOR), Yin, Geng2 (AUTHOR) yingeng1975@163.com, Xie, Qibing1 (AUTHOR) xieqibing1971@163.com
Publikováno v: Skeletal Muscle. 7/18/2024, Vol. 14 Issue 1, p1-14. 14p.
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9
Akademický článek
A Review of Myositis-Associated Interstitial Lung Disease.
Autor: Kannappan, Renuka1 (AUTHOR) renuka.kannappan@tuhs.temple.edu, Kumar, Raagni1 (AUTHOR), Cichelli, Kimberly2 (AUTHOR), Brent, Lawrence H.2 (AUTHOR) renuka.kannappan@tuhs.temple.edu
Publikováno v: Journal of Clinical Medicine. Jul2024, Vol. 13 Issue 14, p4055. 25p.
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10
DNMT3B mutations and DNA methylation defect define two types of ICF syndrome
Autor: Y L, Jiang, M, Rigolet, D, Bourc'his, F, Nigon, I, Bokesoy, J P, Fryns, M, Hultén, P, Jonveaux, P, Maraschio, A, Mégarbané, A, Moncla, E, Viegas-Péquignot
Publikováno v: Human mutation. 25(1)
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centromeric instability, and facial abnormalities. Mutations in the catalytic domain of DNMT3B, a gene encoding a de novo DNA methyltransferase, have been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c5dcf2adafd2d0dbb45beed0a56de69a
https://pubmed.ncbi.nlm.nih.gov/15580563
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