Kibiryeva N - Search Results

1

Snord94 expression level alters methylation at C62 in snRNA U6.

Ogren A, Kibiryeva N, Marshall J, O'Brien JE Jr, Bittel DC. Ogren A, et al. Among authors: kibiryeva n. PLoS One. 2019 Dec 5;14(12):e0226035. doi: 10.1371/journal.pone.0226035. eCollection 2019. PLoS One. 2019. PMID: 31805133 Free PMC article.

2

Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot.

Bittel DC, Zhou XG, Kibiryeva N, Fiedler S, O'Brien JE Jr, Marshall J, Yu S, Liu HY. Bittel DC, et al. Among authors: kibiryeva n. PLoS One. 2014 Jan 31;9(1):e87472. doi: 10.1371/journal.pone.0087472. eCollection 2014. PLoS One. 2014. PMID: 24498113 Free PMC article. Clinical Trial.

3

scaRNA1 Levels Alter Pseudouridylation in Spliceosomal RNA U2 Affecting Alternative mRNA Splicing and Embryonic Development.

Nagasawa CK, Kibiryeva N, Marshall J, O'Brien JE Jr, Bittel DC. Nagasawa CK, et al. Among authors: kibiryeva n. Pediatr Cardiol. 2020 Feb;41(2):341-349. doi: 10.1007/s00246-019-02263-4. Epub 2020 Jan 17. Pediatr Cardiol. 2020. PMID: 31953571

4

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Butler MG. Bittel DC, et al. Among authors: kibiryeva n. Pediatrics. 2006 Oct;118(4):e1276-83. doi: 10.1542/peds.2006-0424. Epub 2006 Sep 18. Pediatrics. 2006. PMID: 16982806 Free PMC article.

5

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome.

Bittel DC, Kibiryeva N, Butler MG. Bittel DC, et al. Among authors: kibiryeva n. Genet Med. 2007 Jul;9(7):464-72. doi: 10.1097/gim.0b013e3180ca9a9a. Genet Med. 2007. PMID: 17666893 Free PMC article. Clinical Trial.

6

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.

Bittel DC, Kibiryeva N, Butler MG. Bittel DC, et al. Among authors: kibiryeva n. Genet Test. 2007 Winter;11(4):467-75. doi: 10.1089/gte.2007.0061. Genet Test. 2007. PMID: 18294067 Free PMC article.

7

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects.

Bittel DC, Butler MG, Kibiryeva N, Marshall JA, Chen J, Lofland GK, O'Brien JE Jr. Bittel DC, et al. Among authors: kibiryeva n. BMC Med Genomics. 2011 Jan 5;4:1. doi: 10.1186/1755-8794-4-1. BMC Med Genomics. 2011. PMID: 21208432 Free PMC article.

8

Noncoding RNA expression in myocardium from infants with tetralogy of Fallot.

O'Brien JE Jr, Kibiryeva N, Zhou XG, Marshall JA, Lofland GK, Artman M, Chen J, Bittel DC. O'Brien JE Jr, et al. Among authors: kibiryeva n. Circ Cardiovasc Genet. 2012 Jun;5(3):279-86. doi: 10.1161/CIRCGENETICS.111.961474. Epub 2012 Apr 23. Circ Cardiovasc Genet. 2012. PMID: 22528145

9

A tissue-specific gene expression template portrays heart development and pathology.

Rodemoyer A, Kibiryeva N, Bair A, Marshall J, O'Brien JE Jr, Bittel DC. Rodemoyer A, et al. Among authors: kibiryeva n. Hum Genomics. 2014 Mar 11;8(1):6. doi: 10.1186/1479-7364-8-6. Hum Genomics. 2014. PMID: 24618031 Free PMC article.

10

MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot.

Bittel DC, Kibiryeva N, Marshall JA, O'Brien JE. Bittel DC, et al. Among authors: kibiryeva n. Cells. 2014 Jul 11;3(3):713-23. doi: 10.3390/cells3030713. Cells. 2014. PMID: 25257024 Free PMC article.

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