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Lactobacillus casei Shirota Supplementation Does Not Restore Gut Microbiota Composition and Gut Barrier in Metabolic Syndrome: A Randomized Pilot Study.
Stadlbauer V, Leber B, Lemesch S, Trajanoski S, Bashir M, Horvath A, Tawdrous M, Stojakovic T, Fauler G, Fickert P, Högenauer C, Klymiuk I, Stiegler P, Lamprecht M, Pieber TR, Tripolt NJ, Sourij H. Stadlbauer V, et al. Among authors: trajanoski s. PLoS One. 2015 Oct 28;10(10):e0141399. doi: 10.1371/journal.pone.0141399. eCollection 2015. PLoS One. 2015. PMID: 26509793 Free PMC article. Clinical Trial.
Free threonine in human breast milk is related to infant intestinal microbiota composition.
Riederer M, Schweighofer N, Trajanoski S, Stelzer C, Zehentner M, Fuchs-Neuhold B, Kashofer K, Mayr JA, Hörmann-Wallner M, Holasek S, van der Kleyn M. Riederer M, et al. Among authors: trajanoski s. Amino Acids. 2022 Mar;54(3):365-383. doi: 10.1007/s00726-021-03057-w. Epub 2021 Sep 3. Amino Acids. 2022. PMID: 34477981 Free PMC article.
Insights into the Composition of a Co-Culture of 10 Probiotic Strains (OMNi BiOTiC® AAD10) and Effects of Its Postbiotic Culture Supernatant.
Kienesberger B, Obermüller B, Singer G, Arneitz C, Gasparella P, Klymiuk I, Horvath A, Stadlbauer V, Magnes C, Zügner E, López-García P, Trajanoski S, Miekisch W, Fuchs P, Till H, Castellani C. Kienesberger B, et al. Among authors: trajanoski s. Nutrients. 2022 Mar 11;14(6):1194. doi: 10.3390/nu14061194. Nutrients. 2022. PMID: 35334850 Free PMC article.
SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients.
Papić L, Fischer D, Trajanoski S, Höftberger R, Fischer C, Ströbel T, Schmidt WM, Bittner RE, Schabhüttl M, Gruber K, Pieber TR, Janecke AR, Auer-Grumbach M. Papić L, et al. Among authors: trajanoski s. Eur J Med Genet. 2011 May-Jun;54(3):214-9. doi: 10.1016/j.ejmg.2010.12.003. Epub 2010 Dec 21. Eur J Med Genet. 2011. PMID: 21172462 Free PMC article.
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.
Guelly C, Zhu PP, Leonardis L, Papić L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, Trajanoski S, Pieber TR, Janecke AR, Blackstone C, Auer-Grumbach M. Guelly C, et al. Among authors: trajanoski s. Am J Hum Genet. 2011 Jan 7;88(1):99-105. doi: 10.1016/j.ajhg.2010.12.003. Epub 2010 Dec 30. Am J Hum Genet. 2011. PMID: 21194679 Free PMC article.
48 results