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Page 1
Comparative Proteomic Assessment of Normal vs. Polyhydramnios Amniotic Fluid Based on Computational Analysis.
Biomedicines. 2022 Jul 28;10(8):1821. doi: 10.3390/biomedicines10081821.
Biomedicines. 2022.
PMID: 36009368
Free PMC article.
Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families.
Preiksaitiene E, Voisin N, Gueneau L, Benušienė E, Krasovskaja N, Blažytė EM, Ambrozaitytė L, Rančelis T, Reymond A, Kučinskas V.
Preiksaitiene E, et al. Among authors: krasovskaja n.
Am J Med Genet A. 2020 Mar;182(3):536-542. doi: 10.1002/ajmg.a.61453. Epub 2019 Dec 12.
Am J Med Genet A. 2020.
PMID: 31833209
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DNA methyltransferases inhibitors effectively induce gene expression changes suggestive of cardiomyogenic differentiation of human amniotic fluid-derived mesenchymal stem cells via chromatin remodeling.
Gasiūnienė M, Zentelytė A, Wojtas B, Baronaitė S, Krasovskaja N, Savickienė J, Gielniewski B, Kaminska B, Utkus A, Navakauskienė R.
Gasiūnienė M, et al. Among authors: krasovskaja n.
J Tissue Eng Regen Med. 2019 Mar;13(3):469-481. doi: 10.1002/term.2800. Epub 2019 Feb 20.
J Tissue Eng Regen Med. 2019.
PMID: 30637987
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R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome.
Preiksaitiene E, Krasovskaja N, Utkus A, Kasnauskiene J, Meškienė R, Paulauskiene I, Valevičienė NR, Kučinskas V.
Preiksaitiene E, et al. Among authors: krasovskaja n.
Clin Dysmorphol. 2015 Jan;24(1):7-12. doi: 10.1097/MCD.0000000000000059.
Clin Dysmorphol. 2015.
PMID: 25304119
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Histone Modifications Pattern Associated With a State of Mesenchymal Stem Cell Cultures Derived From Amniotic Fluid of Normal and Fetus-Affected Gestations.
Savickienė J, Matuzevičius D, Baronaitė S, Treigytė G, Krasovskaja N, Zaikova I, Navakauskas D, Utkus A, Navakauskienė R.
Savickienė J, et al. Among authors: krasovskaja n.
J Cell Biochem. 2017 Nov;118(11):3744-3755. doi: 10.1002/jcb.26022. Epub 2017 May 30.
J Cell Biochem. 2017.
PMID: 28379622
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Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report.
Aleksiūnienė B, Matulevičiūtė R, Matulevičienė A, Burnytė B, Krasovskaja N, Ambrozaitytė L, Mikštienė V, Dirsė V, Utkus A, Kučinskas V.
Aleksiūnienė B, et al. Among authors: krasovskaja n.
Medicine (Baltimore). 2017 Apr;96(16):e6521. doi: 10.1097/MD.0000000000006521.
Medicine (Baltimore). 2017.
PMID: 28422838
Free PMC article.
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