Zobrazeno 1 - 8
of 8
pro vyhledávání: '"PLCXD3"'
Autor:
Hayat Aljaibeji, Debasmita Mukhopadhyay, Abdul Khader Mohammed, Sarah Dhaiban, Mahmood Y. Hachim, Noha M. Elemam, Nabil Sulaiman, Albert Salehi, Jalal Taneera
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Previous work has shown that reduced expression of PLCXD3, a member of the phosphoinositide-specific phospholipases (PI-PLC) family, impaired insulin secretion with an unclear mechanism. In the current study, we aim to investigate the mechanism under
Externí odkaz:
https://doaj.org/article/55019bc111574dcb8c6929f5a1fa0aee
Autor:
Sarah Dhaiban, Nabil Sulaiman, Jalal Taneera, Albert Salehi, Debasmita Mukhopadhyay, Noha Mousaad Elemam, Mahmood Y. Hachim, Abdul Khader Mohammed, Hayat Aljaibeji
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Previous work has shown that reduced expression of PLCXD3, a member of the phosphoinositide-specific phospholipases (PI-PLC) family, impaired insulin secretion with an unclear mechanism. In the current study, we aim to investigate the mechanism under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a452dfd2201e665a4fd104d6c6ffc82
https://doi.org/10.3389/fendo.2019.00735
https://doi.org/10.3389/fendo.2019.00735
Publikováno v:
Oncotarget
// Zhiming Li 1,2 , Zaozao Zheng 1,2 , Jun Ruan 1,2 , Zhi Li 1,2 , Xuan Zhuang 4 and Chi-Meng Tzeng 1,2,3 1 Translational Medicine Research Center (TMRC), School of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian, China 2 Key Laboratory fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8242c256ae9d43e78a697e0ba6c97014
https://pubmed.ncbi.nlm.nih.gov/27486773
https://pubmed.ncbi.nlm.nih.gov/27486773
Autor:
Balendra, Rubika, Uphill, James, Collinson, Claire, Druyeh, Ronald, Adamson, Gary, Hummerich, Holger, Zerr, Inga, Gambetti, Pierluigi, Collinge, John, Mead, Simon
Publikováno v:
BMC medical genetics 17(1), 28 (2016). doi:10.1186/s12881-016-0278-2
BMC Medical Genetics
BMC Medical Genetics
Background Human prion diseases are relentlessly progressive neurodegenerative disorders which include sporadic Creutzfeldt-Jakob disease (sCJD) and variant CJD (vCJD). Aside from variants of the prion protein gene (PRNP) replicated association at ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9b847810d2af54ab2fd141e3d0be061f
https://pub.dzne.de/record/138482
https://pub.dzne.de/record/138482
Akademický článek
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Autor:
Nicolas, Aude
Affectant plus de 1% de la population, les troubles bipolaires constituent l'une des maladies mentales les plus fréquentes, sévères et dévastatrices. Ces troubles de l’humeur se caractérisent par une alternance d’épisodes maniaques (humeur
Externí odkaz:
http://www.theses.fr/2011PEST0095/document
Autor:
Nicolas, Aude
Publikováno v:
Médecine humaine et pathologie. Université Paris-Est, 2011. Français. ⟨NNT : 2011PEST0095⟩
Bipolar Affective Disorder (BPAD) is a common, severe and fatal psychiatric disease, affecting approximately 1% of general population. Despite a demonstrated genetic component, genetic studies have difficulties in identifying vulnerability genes, bec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a8f7e88e69e377f8d90aecbdce13dc74
https://tel.archives-ouvertes.fr/tel-01124049
https://tel.archives-ouvertes.fr/tel-01124049
Akademický článek
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