about
A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy.Functional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birthCytokines, implantation and early abortion: re-examining the Th1/Th2 paradigm leads to question the single pathway, single therapy concept.The -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortionY chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review.A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses.Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis.Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion.Demonstration of the presence of IL-16, IL-17 and IL-18 at the murine fetomaternal interface during murine pregnancy.Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion.Matrix metalloproteinase and tissue inhibitors of metalloproteinases gene polymorphisms in disorders that influence fertility and pregnancy complications: A systematic review and meta-analysis.Secular change in body height and cephalic index of Croatian medical students (University of Rijeka).Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion.A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion.Genetic predisposition to idiopathic recurrent spontaneous abortion: contribution of genetic variations in IGF-2 and H19 imprinted genes.Secular change of craniofacial measures in Croatian younger adults.New insights into maternal-fetal interactions at implantation.Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion.Genetic polymorphisms of 15 STR loci in the population of the island of Cres (Croatia).Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion.Sex-specific differences of craniofacial traits in Croatia: The impact of environment in a small geographic areaPolymorphisms in the interleukin-12/18 genes and recurrent spontaneous abortionCornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: comments on the article by Pereza et al. [2012]
P50
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P50
description
Forscher
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investigador
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onderzoeker
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researcher
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հետազոտող
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研究者
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name
Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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Saša Ostojić
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P106
P1153
6603959759
P31
P496
0000-0001-7134-4335