Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Fabrice Daubigney"'
Autor:
Céline Cruciani-Guglielmacci, Kelly Meneyrol, Jessica Denom, Nadim Kassis, Latif Rachdi, Fatna Makaci, Stéphanie Migrenne-Li, Fabrice Daubigney, Eleni Georgiadou, Raphaël G. Denis, Ana Rodriguez Sanchez-Archidona, Jean-Louis Paul, Bernard Thorens, Guy A. Rutter, Christophe Magnan, Hervé Le Stunff, Nathalie Janel
Publikováno v:
Cells, Vol 11, Iss 11, p 1737 (2022)
Cystathionine beta synthase (CBS) catalyzes the first step of the transsulfuration pathway from homocysteine to cystathionine, and its deficiency leads to hyperhomocysteinemia (HHcy) in humans and rodents. To date, scarce information is available abo
Externí odkaz:
https://doaj.org/article/e39e5da75b8443ba9489a6fbff84e319
Autor:
Alizée Latour, Sacha Salameh, Christel Carbonne, Fabrice Daubigney, Jean-Louis Paul, Micheline Kergoat, Valérie Autier, Jean-Maurice Delabar, Bart De Geest, Nathalie Janel
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 2, Iss C, Pp 51-60 (2015)
Hyperhomocysteinemia results from hepatic metabolism dysfunction and is characterized by a high plasma homocysteine level, which is also an independent risk factor for cardiovascular disease. Elevated levels of homocysteine in plasma lead to hepatic
Externí odkaz:
https://doaj.org/article/52a5c705baee415583f8516c24f2a8e4
Autor:
Benoit Souchet, Fayçal Guedj, Ignasi Sahún, Arnaud Duchon, Fabrice Daubigney, Anne Badel, Yuchio Yanagawa, Maria Jose Barallobre, Mara Dierssen, Eugene Yu, Yann Herault, Mariona Arbones, Nathalie Janel, Nicole Créau, Jean Maurice Delabar
Publikováno v:
Neurobiology of Disease, Vol 69, Iss , Pp 65-75 (2014)
Cognitive deficits in Down syndrome (DS) have been linked to increased synaptic inhibition, leading to an imbalance of excitation/inhibition (E/I). Various mouse models and studies from human brains have implicated an HSA21 gene, the serine/threonine
Externí odkaz:
https://doaj.org/article/38eb53d8da744590b164b4cc0d3230c4
Autor:
Yuchen Gu, Valérie Nalesso, Yuejin Yu, Julien Dairou, Yann Herault, Jean-Maurice Delabar, Nicole Créau, Fabrice Daubigney, Arnaud Duchon, Benoit Souchet, Claire Chevalier, Nathalie Janel
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9, pp.3914. ⟨10.1038/s41598-019-40328-9⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9, pp.3914. ⟨10.1038/s41598-019-40328-9⟩
Down syndrome is a common genetic disorder caused by trisomy of chromosome 21. Brain development in affected foetuses might be improved through prenatal treatment. One potential target is DYRK1A, a multifunctional kinase encoded by chromosome 21 that
Autor:
Michel Mallat, Fabrice Daubigney, Catherine Colin, Sandrine Middendorp, Jean-Christophe Rain, Nadim Kassis, Valerie Hindie, M.L. Arbonés, Blandine Gausserès, Jean-Maurice Delabar, Jean-Louis Paul, Nathalie Janel, Yuchen Gu, Eugene Yu, Alizée Latour
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2019, 56 (2), pp.963-975. ⟨10.1007/s12035-018-1113-x⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecular Neurobiology, Humana Press, 2019, 56 (2), pp.963-975. ⟨10.1007/s12035-018-1113-x⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
International audience; Down syndrome is characterized by premature aging and dementia with neurological features that mimic those found in Alzheimer's disease. This pathology in Down syndrome could be related to inflammation, which plays a role in o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab1f26769338a1ae350f08e7f4bdceea
https://hal-cnrs.archives-ouvertes.fr/hal-03201563
https://hal-cnrs.archives-ouvertes.fr/hal-03201563
Autor:
Fabrice Daubigney, Marjorie Renon, Marie Mortreux, Jean-Maurice Delabar, Etienne Blanc, Jean-Louis Paul, Cindy Bokobza, Béatrice Le-Grand, Hélène Rouach, Karine Andreau, Nathalie Janel
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862:1495-1503
Alcoholic liver diseases arise from complex phenotypes involving many genetic factors. It is quite common to find hyperhomocysteinemia in chronic alcoholic liver diseases, mainly due to deregulation of hepatic homocysteine metabolism. Dyrk1A, involve
Publikováno v:
Experimental and Toxicologic Pathology. 68:365-370
Homocysteine, a sulfur-containing amino acid formed during the metabolism of methionine, is commonly slightly elevated in the plasma of the general population. Additionally, we previously found that cystathionine beta synthase-deficient mice, a murin
Autor:
Fabrice Daubigney, Jacqueline London, F K Ndiaye, Julien Dairou, Nathalie Janel, Linh-Chi Bui, Benoit Souchet, Christophe Magnan, Claude Rouch, Serge Luquet
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2019, 56 (6), pp.3958-3971. ⟨10.1007/s12035-018-1323-2⟩
Molecular Neurobiology, Humana Press, 2019, 56 (6), pp.3958-3971. ⟨10.1007/s12035-018-1323-2⟩
Cystathionine beta synthase (CBS) is one of the 225 genes on chromosome 21 (HSA 21) that are triplicated in persons with trisomy 21 (Down syndrome). Although most triplicate HSA21 genes have their orthologous genes on murine chromosome 16, the murine
Autor:
Julien Dairou, Jacqueline London, Benoit Souchet, Linh Chi Bui, Fabrice Daubigney, Christophe Magnan, Nathalie Janel, Serge Luquet, Jean-Maurice Delabar, Hind Medjaoui, Elodie Assayag, Claude Rouch
Publikováno v:
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2018, 55, pp.3822-3831. ⟨10.1007/s12035-017-0591-6⟩
Molecular Neurobiology, Humana Press, 2018, 55, pp.3822-3831. ⟨10.1007/s12035-017-0591-6⟩
International audience; Trisomy 21 (T21) or Down syndrome (DS) is the most common genetic disorder associated with intellectual disability and affects around 5 million persons worldwide. Neuroanatomical phenotypes associated with T21 include slight r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3180c76ec84b333056e81dc85461e1d
https://hal-cnrs.archives-ouvertes.fr/hal-03105437
https://hal-cnrs.archives-ouvertes.fr/hal-03105437
Autor:
Eugene Yu, Yann Herault, Mara Dierssen, Jean-Maurice Delabar, Nathalie Janel, Fabrice Daubigney, Nicole Créau, M.L. Arbonés, Ignasi Sahún, Arnaud Duchon, Maria Jose Barallobre, Benoit Souchet, Faycal Guedj, Yuchio Yanagawa, Anne Badel
Publikováno v:
Neurobiology of Disease, Vol 69, Iss, Pp 65-75 (2014)
Cognitive deficits in Down syndrome (DS) have been linked to increased synaptic inhibition, leading to an imbalance of excitation/inhibition (E/I). Various mouse models and studies from human brains have implicated an HSA21 gene, the serine/threonine