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Nataliya Kibiryeva

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Genetic Testing|February 26, 2008
Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalitiesDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Pediatrics|September 20, 2006
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
Whole genome microarray analysis of gene expression in subjects with fragile X syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2006
C-reactive protein levels in subjects with Prader-Willi syndrome and obesityMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndromeMerlin G Butler, William Fischer, Nataliya Kibiryeva, et al.
International Journal of Molecular Medicine|March 9, 2005
Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndromeZohreh Talebizadeh, Nataliya Kibiryeva, Douglas C Bittel, et al.
Cells|September 27, 2014
MicroRNA-421 Dysregulation is Associated with Tetralogy of FallotDouglas C Bittel, Nataliya Kibiryeva, Jennifer A Marshall, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 11, 2012
Pleiotropic functions of pre-B-cell colony-enhancing factor (PBEF) revealed by transcriptomics of human pulmonary microvascular endothelial cells treated with PBEFsiRNADilyara Cheranova, Margaret Gibson, Nataliya Kibiryeva, et al.
Plos One|December 6, 2019
Snord94 expression level alters methylation at C62 in snRNA U6Allison Ogren, Nataliya Kibiryeva, Jennifer Marshall, et al.
Pediatrics|March 3, 2004
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomyMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Genetic Testing|February 26, 2008
Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalitiesDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Pediatrics|September 20, 2006
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
Whole genome microarray analysis of gene expression in subjects with fragile X syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G Butler
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2006
C-reactive protein levels in subjects with Prader-Willi syndrome and obesityMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndromeMerlin G Butler, William Fischer, Nataliya Kibiryeva, et al.
International Journal of Molecular Medicine|March 9, 2005
Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndromeZohreh Talebizadeh, Nataliya Kibiryeva, Douglas C Bittel, et al.
Cells|September 27, 2014
MicroRNA-421 Dysregulation is Associated with Tetralogy of FallotDouglas C Bittel, Nataliya Kibiryeva, Jennifer A Marshall, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 11, 2012
Pleiotropic functions of pre-B-cell colony-enhancing factor (PBEF) revealed by transcriptomics of human pulmonary microvascular endothelial cells treated with PBEFsiRNADilyara Cheranova, Margaret Gibson, Nataliya Kibiryeva, et al.
Plos One|December 6, 2019
Snord94 expression level alters methylation at C62 in snRNA U6Allison Ogren, Nataliya Kibiryeva, Jennifer Marshall, et al.
Pediatrics|March 3, 2004
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomyMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
Pageof 4