Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jasmine, Butler"'
Autor:
Virginie, Marty, Jasmine, Butler, Coutens, Basile, Oumaima, Chargui, Abdeslam, Chagraoui, Bruno P, Guiard, Philippe, De Deurwaerdère, Jérôme, Cavaillé
Publikováno v:
Human Molecular Genetics. 32:244-261
The neuronal-specific SNORD115 has gathered interest because its deficiency may contribute to the pathophysiology of Prader-Willi syndrome (PWS), possibly by altering post-transcriptional regulation of the gene encoding the serotonin (HTR2C) receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b79422b39db7580d394576a008ba3b7
https://doi.org/10.1093/hmg/ddac139
https://doi.org/10.1093/hmg/ddac139
Autor:
Hugo Martin, Sébastien Bullich, Maud Martinat, Mathilde Chataigner, Mathieu Di Miceli, Vincent Simon, Samantha Clark, Jasmine Butler, Mareike Schell, Simran Chopra, Francis Chaouloff, Andre Kleinridders, Daniela Cota, Philippe De Deurwaerdere, Luc Pénicaud, Sophie Layé, Bruno P. Guiard, Xavier Fioramonti
Publikováno v:
Molecular Psychiatry.
Type-2 Diabetes (T2D) is characterized by insulin resistance and accompanied by psychiatric comorbidities including major depressive disorders (MDD). Patients with T2D are twice more likely to suffer from MDD and clinical studies have shown that insu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::067a1c009dd13b2017a37abd87e282bb
https://doi.org/10.1038/s41380-022-01812-3
https://doi.org/10.1038/s41380-022-01812-3
Publikováno v:
Journal of dentistry for children (Chicago, Ill.). 88(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25751e28bff7fadb260c1e763b6ce216
https://pubmed.ncbi.nlm.nih.gov/34937627
https://pubmed.ncbi.nlm.nih.gov/34937627