Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lara Slavec"'
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-14 (2022)
Abstract To date, the involvement of various genetic markers in the aetiopathogenesis of non-syndromic orofacial cleft (nsOFC) has been extensively studied. In the present study, we focused on studies performed on populations of European ancestry to
Externí odkaz:
https://doaj.org/article/db445ddac69343cdabcf2bcc46e0dc72
Publikováno v:
Slovenska pediatrija, Vol 27, Iss 4, Pp 163-171 (2020)
Human genetic variants occur throughout the whole genome, both in the coding and non-coding regions. In addition to defining genetic diversity among individuals, they may, in some instances, cause various genetic diseases, many of which have their on
Externí odkaz:
https://doaj.org/article/54d24acfe07b430aa1ffa1c76fce2e15
Publikováno v:
Slovenska pediatrija, Vol 27, Iss 4, Pp 163-171 (2020)
Humane genetske spremembe se pojavljajo v celotnem genomu, tako v kodirajočih kot tudi v nekodirajočih predelih. Opredeljujejo genetsko raznolikost med posamezniki in so v nekaterih primerih lahko vzrok različnih genetskih bolezni. ctevilne se poj
Externí odkaz:
https://doaj.org/article/48940eb09d804a9a9f100acd0ee22618
Autor:
Mikael V. Ringh, Michael Hagemann-Jensen, Maria Needhamsen, Lara Kular, Charles E. Breeze, Louise K. Sjöholm, Lara Slavec, Susanna Kullberg, Jan Wahlström, Johan Grunewald, Boel Brynedal, Yun Liu, Malin Almgren, Maja Jagodic, Johan Öckinger, Tomas J. Ekström
Publikováno v:
EBioMedicine, Vol 46, Iss , Pp 290-304 (2019)
Background: While smoking is known to associate with development of multiple diseases, the underlying mechanisms are still poorly understood. Tobacco smoking can modify the chemical integrity of DNA leading to changes in transcriptional activity, par
Externí odkaz:
https://doaj.org/article/1cafb6ec21624987acffe696bc1a2a84
Publikováno v:
Molecules, Vol 26, Iss 21, p 6585 (2021)
Quinazolinones represent an important scaffold in medicinal chemistry with diverse biological activities. Here, two series of 2-substituted quinazolin-4(3H)-ones were synthesized and evaluated for their antioxidant properties using three different me
Externí odkaz:
https://doaj.org/article/e73e428c490f4cc191f015f12b1a5666
Autor:
Lara Slavec, Ksenija Geršak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
Publikováno v:
International journal of molecular sciences, 19 str. : Ilustr., Vol. 24, iss. 5, art. 4262, 2023
COBISS-ID: 2779162
International journal of molecular sciences, vol. 24, no. 5, 4262, 2023.
International Journal of Molecular Sciences
Volume 24
Issue 5
Pages: 4262
COBISS-ID: 2779162
International journal of molecular sciences, vol. 24, no. 5, 4262, 2023.
International Journal of Molecular Sciences
Volume 24
Issue 5
Pages: 4262
Although the aetiology of non-syndromic orofacial clefts (nsOFCs) is usually multifactorial, syndromic OFCs (syOFCs) are often caused by single mutations in known genes. Some syndromes, e.g., Van der Woude syndrome (VWS1; VWS2) and X-linked cleft pal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808d11b415afdc5f6ab3cd46197d0756
https://plus.cobiss.net/cobiss/si/en/bib/142479875
https://plus.cobiss.net/cobiss/si/en/bib/142479875
Publikováno v:
Slovenska pediatrija, Vol 27, Iss 4, Pp 163-171 (2020)
Human genetic variants occur throughout the whole genome, both in the coding and non-coding regions. In addition to defining genetic diversity among individuals, they may, in some instances, cause various genetic diseases, many of which have their on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::813bd0227014229cec5261bd6896a9f9
https://doaj.org/article/54d24acfe07b430aa1ffa1c76fce2e15
https://doaj.org/article/54d24acfe07b430aa1ffa1c76fce2e15
Publikováno v:
Slovenska pediatrija, Vol 27, Iss 4, Pp 163-171 (2020)
Humane genetske spremembe se pojavljajo v celotnem genomu, tako v kodirajočih kot tudi v nekodirajočih predelih. Opredeljujejo genetsko raznolikost med posamezniki in so v nekaterih primerih lahko vzrok različnih genetskih bolezni. ctevilne se poj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e1c9958ee7e6b6ec931c19407a1c56
https://doi.org/10.38031/slovpediatr-2020-4-01
https://doi.org/10.38031/slovpediatr-2020-4-01
Autor:
Susanna Kullberg, Boel Brynedal, Yun Liu, Malin Almgren, Lara Slavec, Charles E. Breeze, Mikael V. Ringh, Maja Jagodic, Michael Hagemann-Jensen, Louise K. Sjöholm, Maria Needhamsen, Johan Öckinger, Jan Wahlström, Tomas J. Ekström, Johan Grunewald, Lara Kular
Publikováno v:
EBioMedicine
Background While smoking is known to associate with development of multiple diseases, the underlying mechanisms are still poorly understood. Tobacco smoking can modify the chemical integrity of DNA leading to changes in transcriptional activity, part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4d9be301843c5f2ead52014d7b75f6
http://europepmc.org/articles/PMC6710853
http://europepmc.org/articles/PMC6710853