Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 27

1.

Snord94 expression level alters methylation at C62 in snRNA U6.

Ogren A, Kibiryeva N, Marshall J, O'Brien JE Jr, Bittel DC.

PLoS One. 2019 Dec 5;14(12):e0226035. doi: 10.1371/journal.pone.0226035. eCollection 2019.

2.

Transcriptome profiling reveals activation of inflammation and apoptosis in the neonatal striatum after deep hypothermic circulatory arrest.

Tu LN, Timms AE, Kibiryeva N, Bittel D, Pastuszko A, Nigam V, Pastuszko P.

J Thorac Cardiovasc Surg. 2019 Sep;158(3):882-890.e4. doi: 10.1016/j.jtcvs.2019.02.091. Epub 2019 Mar 6.

PMID:
31005300
3.

The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development.

Nagasawa C, Ogren A, Kibiryeva N, Marshall J, O'Brien JE, Kenmochi N, Bittel DC.

J Cardiovasc Dev Dis. 2018 May 8;5(2). pii: E26. doi: 10.3390/jcdd5020026. Review.

4.

scaRNAs regulate splicing and vertebrate heart development.

Patil P, Kibiryeva N, Uechi T, Marshall J, O'Brien JE Jr, Artman M, Kenmochi N, Bittel DC.

Biochim Biophys Acta. 2015 Aug;1852(8):1619-29. doi: 10.1016/j.bbadis.2015.04.016. Epub 2015 Apr 23.

5.

MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot.

Bittel DC, Kibiryeva N, Marshall JA, O'Brien JE.

Cells. 2014 Jul 11;3(3):713-23. doi: 10.3390/cells3030713.

6.

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.

Hum Genomics. 2014 Mar 11;8:6. doi: 10.1186/1479-7364-8-6.

7.

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.

PLoS One. 2014 Jan 31;9(1):e87472. doi: 10.1371/journal.pone.0087472. eCollection 2014. Erratum in: PLoS One. 2014;9(5):e99148.

8.

Expression and regulation of nampt in human islets.

Kover K, Tong PY, Watkins D, Clements M, Stehno-Bittel L, Novikova L, Bittel D, Kibiryeva N, Stuhlsatz J, Yan Y, Ye SQ, Moore WV.

PLoS One. 2013;8(3):e58767. doi: 10.1371/journal.pone.0058767. Epub 2013 Mar 11.

9.

Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome.

Le Pichon JB, Yu S, Kibiryeva N, Graf WD, Bittel DC.

Eur J Hum Genet. 2013 Oct;21(10):1093-9. doi: 10.1038/ejhg.2013.1. Epub 2013 Jan 30.

10.

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.

Circ Cardiovasc Genet. 2012 Jun;5(3):279-86. doi: 10.1161/CIRCGENETICS.111.961474. Epub 2012 Apr 23.

PMID:
22528145
11.

Pleiotropic functions of pre-B-cell colony-enhancing factor (PBEF) revealed by transcriptomics of human pulmonary microvascular endothelial cells treated with PBEFsiRNA.

Cheranova D, Gibson M, Kibiryeva N, Zhang LQ, Ye SQ.

Genes Cells. 2012 May;17(5):420-30. doi: 10.1111/j.1365-2443.2012.01598.x. Epub 2012 Apr 9.

12.

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.

BMC Med Genomics. 2011 Jan 5;4:1. doi: 10.1186/1755-8794-4-1.

13.

An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.

Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S.

Am J Med Genet A. 2010 Feb;152A(2):404-8. doi: 10.1002/ajmg.a.33197. Erratum in: Am J Med Genet A. 2010 May;152A(5):1331-2.

14.

Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.

Yu S, Kielt M, Stegner AL, Kibiryeva N, Bittel DC, Cooley LD.

Genet Test Mol Biomarkers. 2009 Dec;13(6):751-60. doi: 10.1089/gtmb.2009.0056.

PMID:
20001581
15.

Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.

Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD.

Am J Clin Pathol. 2009 Sep;132(3):349-60. doi: 10.1309/AJCP1BOUTWF6ERYS.

PMID:
19687311
16.

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

Bittel DC, Kibiryeva N, Butler MG.

Genet Test. 2007 Winter;11(4):467-75. doi: 10.1089/gte.2007.0061.

17.

Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.

Butler MG, Fischer W, Kibiryeva N, Bittel DC.

Am J Med Genet A. 2008 Apr 1;146A(7):854-60. doi: 10.1002/ajmg.a.32249.

18.

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

Bittel DC, Kibiryeva N, Butler MG.

Genet Med. 2007 Jul;9(7):464-72.

19.

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Sell SM, Strong TV, Butler MG.

Am J Med Genet A. 2007 Mar 1;143A(5):430-42.

20.

Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.

Bittel DC, Kibiryeva N, McNulty SG, Driscoll DJ, Butler MG, White RA.

Am J Med Genet A. 2007 Mar 1;143A(5):422-9.

Supplemental Content

Loading ...
Support Center