Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lucian Mihai Antoci"'
Autor:
Andreea Florea, Lavinia Caba, Ana-Maria Grigore, Lucian-Mihai Antoci, Mihaela Grigore, Mihaela I. Gramescu, Eusebiu Vlad Gorduza
Publikováno v:
Life, Vol 13, Iss 12, p 2314 (2023)
A hydatidiform mole (HM) or molar pregnancy is the most common benign form of gestational trophoblastic disease characterized by a proliferation of the trophoblastic epithelium and villous edema. Hydatidiform moles are classified into two forms: comp
Externí odkaz:
https://doaj.org/article/02c10636fc604b2fbac6ae914334d69c
Autor:
Karina-Alexandra Cojocaru, Ionut Luchian, Ancuta Goriuc, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Roxana Popescu, Cristiana-Elena Vlad, Mihaela Blaj, Liliana Georgeta Foia
Publikováno v:
Antioxidants, Vol 12, Iss 3, p 658 (2023)
Mitochondria are subcellular organelles involved in essential cellular functions, including cytosolic calcium regulation, cell apoptosis, and reactive oxygen species production. They are the site of important biochemical pathways, including the trica
Externí odkaz:
https://doaj.org/article/7ceb9af7892347e2b0a7646663f812b7
Autor:
Ovidiu-Dumitru Ilie, Raluca Duta, Ioana-Miruna Balmus, Alexandra Savuca, Adriana Petrovici, Ilinca-Bianca Nita, Lucian-Mihai Antoci, Roxana Jijie, Cosmin-Teodor Mihai, Alin Ciobica, Mircea Nicoara, Roxana Popescu, Romeo Dobrin, Carmen Solcan, Anca Trifan, Carol Stanciu, Bogdan Doroftei
Publikováno v:
Antioxidants, Vol 11, Iss 10, p 2040 (2022)
Parkinson’s disease (PD) is an enigmatic neurodegenerative disorder that is currently the subject of extensive research approaches aiming at deepening the understanding of its etiopathophysiology. Recent data suggest that distinct compounds used ei
Externí odkaz:
https://doaj.org/article/4e0d289799a54a638dac2e559d6a0334
Autor:
Eva-Cristiana Gavril, Irina Nucă, Monica-Cristina Pânzaru, Anca Viorica Ivanov, Cosmin-Teodor Mihai, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Cristina Rusu, Roxana Popescu
Publikováno v:
Genes
Volume 14
Issue 2
Pages: 465
Volume 14
Issue 2
Pages: 465
2q37 microdeletion/deletion syndrome (2q37DS) is one of the most common subtelomeric deletion disorders, caused by a 2q37 deletion of variable size. The syndrome is characterized by a broad and diverse spectrum of clinical findings: characteristic fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457f49c938b266752e5c01e8971afcfe
https://doi.org/10.3390/genes14020465
https://doi.org/10.3390/genes14020465
Autor:
Alexandra Maștaleru, Sabina Alexandra Cojocariu, Andra Oancea, Maria Magdalena Leon Constantin, Mihai Roca, Ioana Mădălina Zota, Irina Abdulan, Cristina Rusu, Roxana Popescu, Lucian Mihai Antoci, Cristian Gabriel Ciobanu, Alexandru Dan Costache, Elena Cojocaru, Florin Mitu
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 3; Pages: 429
(1) Background: Familial hypercholesterolemia (FH) is one of the most prevalent inherited metabolic disorders. The purpose of the study was to investigate the role in cardiovascular disease (CVD) of PAI-1, ACE, ApoB-100, MTHFR A1298C, and C677T. (2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bddf89ec7f3f0e6b328d9704a6d5dabd
https://doi.org/10.3390/jpm12030429
https://doi.org/10.3390/jpm12030429