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Year | Number of Results |
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2018 | 1 |
2019 | 1 |
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Page 1
BH4-deficient hyperphenylalaninemia in Russia.
PLoS One. 2021 Apr 6;16(4):e0249608. doi: 10.1371/journal.pone.0249608. eCollection 2021.
PLoS One. 2021.
PMID: 33822819
Free PMC article.
Mitochondrial Dysfunction and Permeability Transition in Neonatal Brain and Lung Injuries.
S Ten V, Stepanova AA, Ratner V, Neginskaya M, Niatsetskaya Z, Sosunov S, Starkov A.
S Ten V, et al. Among authors: stepanova aa.
Cells. 2021 Mar 5;10(3):569. doi: 10.3390/cells10030569.
Cells. 2021.
PMID: 33807810
Free PMC article.
Review.
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Genotypes of 2579 patients with phenylketonuria reveal a high rate of BH4 non-responders in Russia.
Gundorova P, Stepanova AA, Kuznetsova IA, Kutsev SI, Polyakov AV.
Gundorova P, et al. Among authors: stepanova aa.
PLoS One. 2019 Jan 22;14(1):e0211048. doi: 10.1371/journal.pone.0211048. eCollection 2019.
PLoS One. 2019.
PMID: 30668579
Free PMC article.
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Rats with a Human Mutation of NFU1 Develop Pulmonary Hypertension.
Niihori M, Eccles CA, Kurdyukov S, Zemskova M, Varghese MV, Stepanova AA, Galkin A, Rafikov R, Rafikova O.
Niihori M, et al. Among authors: stepanova aa.
Am J Respir Cell Mol Biol. 2020 Feb;62(2):231-242. doi: 10.1165/rcmb.2019-0065OC.
Am J Respir Cell Mol Biol. 2020.
PMID: 31461310
Free PMC article.
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Developmental window of vulnerability to white matter injury driven by sublethal intermittent hypoxemia.
Sosunov SA, Niatsetskaya ZV, Stepanova AA, Galkin AS, Juliano CE, Ratner VI, Ten VS.
Sosunov SA, et al. Among authors: stepanova aa.
Pediatr Res. 2022 May;91(6):1383-1390. doi: 10.1038/s41390-021-01555-x. Epub 2021 May 4.
Pediatr Res. 2022.
PMID: 33947998
Free PMC article.
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Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population.
Kadyshev VV, Alekseeva EA, Strelnikov VV, Stepanova AA, Polyakov AV, Marakhonov AV, Kutsev SI, Zinchenko RA.
Kadyshev VV, et al. Among authors: stepanova aa.
Int J Mol Sci. 2023 Nov 12;24(22):16231. doi: 10.3390/ijms242216231.
Int J Mol Sci. 2023.
PMID: 38003421
Free PMC article.
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Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus.
Gundorova P, Zinchenko RA, Kuznetsova IA, Bliznetz EA, Stepanova AA, Polyakov AV.
Gundorova P, et al. Among authors: stepanova aa.
PLoS One. 2018 Aug 1;13(8):e0201489. doi: 10.1371/journal.pone.0201489. eCollection 2018.
PLoS One. 2018.
PMID: 30067850
Free PMC article.
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