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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.
Maver A, Lavtar P, Ristić S, Stopinšek S, Simčič S, Hočevar K, Sepčić J, Drulović J, Pekmezović T, Novaković I, Alenka H, Rudolf G, Šega S, Starčević-Čizmarević N, Palandačić A, Zamolo G, Kapović M, Likar T, Peterlin B. Maver A, et al. Among authors: hocevar k. Sci Rep. 2017 Jun 16;7(1):3715. doi: 10.1038/s41598-017-03536-9. Sci Rep. 2017. PMID: 28623311 Free PMC article.
The Endometrial Transcriptome of Metabolic and Inflammatory Pathways During the Window of Implantation Is Deranged in Infertile Obese Polycystic Ovarian Syndrome Women.
Salamun V, Rizzo M, Lovrecic L, Hocevar K, Papler Burnik T, Janez A, Jensterle M, Vrtacnik Bokal E, Peterlin B, Maver A. Salamun V, et al. Among authors: hocevar k. Metab Syndr Relat Disord. 2022 Sep;20(7):384-394. doi: 10.1089/met.2021.0149. Epub 2022 Jul 13. Metab Syndr Relat Disord. 2022. PMID: 35834645
Integrative transcriptomic analysis in human and mouse model of anaphylaxis identifies gene signatures associated with cell movement, migration and neuroinflammatory signalling.
Rijavec M, Maver A, Turner PJ, Hočevar K, Košnik M, Yamani A, Hogan SP, Custovic A, Peterlin B, Korošec P. Rijavec M, et al. Among authors: hocevar k. Front Immunol. 2022 Dec 8;13:1016165. doi: 10.3389/fimmu.2022.1016165. eCollection 2022. Front Immunol. 2022. PMID: 36569939 Free PMC article. Clinical Trial.
Oral microbiome and preterm birth.
Vidmar Šimic M, Maver A, Zimani AN, Hočevar K, Peterlin B, Kovanda A, Premru-Sršen T. Vidmar Šimic M, et al. Among authors: hocevar k. Front Med (Lausanne). 2023 Aug 7;10:1177990. doi: 10.3389/fmed.2023.1177990. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37608830 Free PMC article.
14 results