Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Marie-Pierre Belot"'
Autor:
Charles de Ponthaud, Solafah Abdalla, Marie-Pierre Belot, Xiaojian Shao, Christophe Penna, Antoine Brouquet, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-9 (2024)
Abstract Background E-cadherin, a major actor of cell adhesion in the intestinal barrier, is encoded by the CDH1 gene associated with susceptibility to Crohn Disease (CD) and colorectal cancer. Since epigenetic mechanisms are suspected to contribute
Externí odkaz:
https://doaj.org/article/810e71583efc49e19aaf6e6df287aa45
Autor:
Charles de Ponthaud, Solafah Abdalla, Marie-Pierre Belot, Xiaojian Shao, Christophe Penna, Antoine Brouquet, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/d67022a1971a4659aae65b4f7a9397c1
Publikováno v:
Epigenetics, Vol 13, Iss 5, Pp 459-472 (2018)
IL2RA, a subunit of the high affinity receptor for interleukin-2 (IL2), plays a crucial role in immune homeostasis. Notably, IL2RA expression is induced in CD4+ T cells in response to various stimuli and is constitutive in regulatory T cells (Tregs).
Externí odkaz:
https://doaj.org/article/6557121c9f9f4a68b948799d296c219a
Autor:
Catherine Le Stunff, Anne-Laure Castell, Nicolas Todd, Clémence Mille, Marie-Pierre Belot, Nathalie Frament, Sylvie Brailly-Tabard, Alexandra Benachi, Delphine Fradin, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-7 (2018)
Abstract Background There are many reasons to think that epigenetics is a key determinant of fetal growth variability across the normal population. Since IGF1 and INS genes are major determinants of intrauterine growth, we examined the methylation of
Externí odkaz:
https://doaj.org/article/257338b79613435aa3252790022c792e
Autor:
Catherine Le Stunff, Anne-Laure Castell, Nicolas Todd, Clémence Mille, Marie-Pierre Belot, Nathalie Frament, Sylvie Brailly-Tabard, Alexandra Benachi, Delphine Fradin, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-1 (2018)
After publication of the original article [1], it came to the publishers’ attention that the below author’s corrections provided at the proofing stage had been misinterpreted.
Externí odkaz:
https://doaj.org/article/2dfa2a22977e4f15a1920e070efc62f5
Autor:
Marie-Pierre Belot, Delphine Fradin, Nga Mai, Sophie Le Fur, Diana Zélénika, Julie Kerr-Conte, François Pattou, Bruno Lucas, Pierre Bougnères
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68093 (2013)
None of the polymorphic variants of the IL2RA gene found associated with Type 1 Diabetes (T1D) was shown to have a functional effect. To test if the epigenetic variation could play a role at this locus, we studied the methylation of 6 CpGs located wi
Externí odkaz:
https://doaj.org/article/f8b224860e7c4313b520da53d9cad5f4
Autor:
Clémence Mille, Alexandra Benachi, Delphine Fradin, Pierre-Yves Boëlle, Kambiz Naderi, Marie-Pierre Belot, Pierre Bougnères
Publikováno v:
Pediatric Diabetes. 18:178-187
Genome-wide association studies (GWAS) have identified more than 40 T1D loci associated with type 1 diabetes (T1D). How these polymorphisms interact with environmental factors to trigger T1D is unknown, but recent evidence suggests that epigenetic me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::143c07afff1deabe0b41848813dc2b16
https://doi.org/10.1111/pedi.12387
https://doi.org/10.1111/pedi.12387
Autor:
Delphine Fradin, Pierre-Yves Boëlle, Marie-Pierre Belot, Fanny Lachaux, Jorg Tost, Céline Besse, Jean-François Deleuze, Gianpaolo De Filippo, Pierre Bougnères
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2017, 7, pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, 2017, 7, pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, 2017, 7 (1), pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, Nature Publishing Group, 2017, 7 (1), pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, Nature Publishing Group, 2017, 7, pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, 2017, 7, pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, 2017, 7 (1), pp.46311. ⟨10.1038/srep46311⟩
Scientific Reports, Nature Publishing Group, 2017, 7 (1), pp.46311. ⟨10.1038/srep46311⟩
International audience; Obesity is a heterogeneous disease with many different subtypes. Epigenetics could contribute to these differences. The aim of this study was to investigate genome-wide DNA methylation searching for methylation marks associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::efbaefbc41a200ea709b2ea746ac1fa6
https://hal.sorbonne-universite.fr/hal-01516806/file/srep46311.pdf
https://hal.sorbonne-universite.fr/hal-01516806/file/srep46311.pdf
Autor:
Clémence Mille, Nicolas Todd, Nathalie Frament, Delphine Fradin, Marie-Pierre Belot, Anne-Laure Castell, Sylvie Brailly-Tabard, Pierre Bougnères, Catherine Le Stunff, Alexandra Benachi
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-1 (2018)
Clinical Epigenetics
Clinical Epigenetics
There are many reasons to think that epigenetics is a key determinant of fetal growth variability across the normal population. SinceCord blood was sampled in 159 newborns born to mothers prospectively followed during their pregnancy. A 142-item ques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5f275937a2a7668a7026771f75b3e53
http://link.springer.com/article/10.1186/s13148-018-0506-z
http://link.springer.com/article/10.1186/s13148-018-0506-z
Autor:
Véronique Machelon, Gérard Tachdjian, Dominique Emilie, Laetitia Hesters, M. Filali, René Frydman, Françoise Gaudin, Marie-Pierre Belot, Nelly Frydman
Publikováno v:
Europe PubMed Central
BCL2-associated X protein (BAX) and B-cell leukaemia/lymphoma gene-2 (BCL2), which are, respectively, pro- and anti-apoptotic proteins of the BCL2 gene family, participate in the mitochondria-dependent apoptosis pathway. A correlation between low inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05990911911dd4dcf4048ccbc9060ed4
https://doi.org/10.1016/s1472-6483(10)61071-1
https://doi.org/10.1016/s1472-6483(10)61071-1