![]() | Ilona Sylvia SkerjancDepartment of Biochemistry, Microbiology, and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada | Department of Biochemistry, Microbiology, and ... |
KOL Resume for Ilona Sylvia Skerjanc
Year | |
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2019 | Department of Biochemistry, Microbiology, and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada |
2018 | Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario, Canada |
2017 | Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, ON K1H 8M5, Canada |
2016 | Department of Biochemistry, Microbiology & Immunology, Roger Guindon Hall, 451 Smyth Road, University of Ottawa, Ottawa, ON, K1N 6N5, Canada |
2015 | Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada |
2013 | Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada |
2012 | From the, Department of Biochemistry, Microbiology, and Immunology and |
2011 | Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, 451 Smyth Road, K1H 8M5, Ottawa, ON, Canada |
2010 | Departments of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada |
2009 | Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario, Canada K1H 8M5 |
2008 | Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada |
2006 | Department of Biochemistry, Medical Sciences Building, University of Western Ontario, London, Ontario, N6A 5C1, Canada |
2005 | Department of Biochemistry, Medical Sciences Building, University of Western Ontario, London, Ontario N6A 5C1, Canada and the |
2004 | Department of Biochemistry, University of Western Ontario, London, Ontario, Canada |
2002 | Department of Biochemistry, Medical Sciences Building, The University of Western Ontario, London, ON, Canada N6A 5C1 |
2001 | Department of Biochemistry Medical Sciences Building University of Western Ontario London, Ontario Canada N6A 5C1 |
2000 | Department of Biochemistry, Medical Sciences Building, University of Western Ontario, London, Ont. N6A 5C1, Canada |
1999 | Department of Biochemistry Medical Sciences Building, University of Western Ontario, N6A 5C1, London, Ontario, Canada |
1996 | Department of Biochemistry, Health Sciences Building, University of Western Ontario, London, Ontario N6A 5C1, Canada |
1995 | Department of Medicine, University of Ottawa and Ottawa Civic Hospital, K1H 8M5, Ottawa, ON, Canada |
1994 | Cancer Research Group, Department of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, Canada, K1H-8M5 |
1993 | Banting and Best Department of Medical Research, Charles H. Best Institute, University of Toronto, Ontario, Canada. |
Ilona Sylvia Skerjanc: Influence Statistics
Concept | World rank |
---|---|
mef2c expression series | #1 |
transient transfection mef2 | #1 |
itf2b itf2a | #1 |
neurogenic properties gli2 | #1 |
signalling mef2c | #1 |
myogenesis stem | #1 |
cardiomyogenesis meox1 | #1 |
initiate cardiomyogenesis | #1 |
meox1 noggin | #1 |
myod activity itf2b | #1 |
model gli2 | #1 |
expression bmp inhibitor | #1 |
gli2 transcripts gli2 | #1 |
mef2c activate | #1 |
mef2cinduced neurons | #1 |
gli2 neurogenesis | #1 |
nkx25 function role | #1 |
mash1 mef2c | #1 |
muscleinducing levels | #1 |
negative meox1 | #1 |
regulates mrf | #1 |
me2soinduced cardiomyogenesis | #1 |
search annotation tool | #1 |
inhibits cardiomyogenesis | #1 |
inhibit myod | #1 |
p19 cells mef2c | #1 |
functions skeletal myogenesis | #1 |
premyogenic mesoderm | #1 |
transient reduction cardiomyogenesis | #1 |
myogenesis bmp4 | #1 |
cardiomyogenesis stem cells | #1 |
events wnt3a | #1 |
gli2 mef2c gene | #1 |
myogenin activate | #1 |
camk gata4 | #1 |
nkx25r141c | #1 |
fulllength e12 e47 | #1 |
pathway timely cardiomyogenesis | #1 |
5 cardiomyogenesis | #1 |
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Prominent publications by Ilona Sylvia Skerjanc
Myocyte Enhancer Factor 2C and Myogenin Up-regulate Each Other's Expression and Induce the Development of Skeletal Muscle in P19 Cells*
[ PUBLICATION ]
Two families of transcription factors, myogenic regulatory factors (MRFs) and myocyte enhancer factor 2 (MEF2), function synergistically to regulate myogenesis. In addition to activating structural muscle-specific genes, MRFs and MEF2 activate each other's expression. The MRF, myogenin, can activate MEF2 DNA binding activity when transfected into fibroblasts and, in turn, the myogenin promoter contains essential MEF2 DNA binding elements. To determine which MEF2 is involved in this ...
Known for P19 Cells | Skeletal Muscle | Myod Myogenin | Myocyte Enhancer | Transcription Factors |
Pax3 is a paired box transcription factor expressed during somitogenesis that has been implicated in initiating the expression of the myogenic regulatory factors during myogenesis. We find that Pax3 is necessary and sufficient to induce myogenesis in pluripotent stem cells. Pax3 induced the expression of the transcription factor Six1, its cofactor Eya2, and the transcription factor Mox1 prior to inducing the expression of MyoD and myogenin. Overexpression of a dominant negative Pax3, ...
Known for Skeletal Myogenesis | Pax3 Expression | Biological Muscle | Developmental Genes | Proteins Models |
Sonic Hedgehog (Shh) is a critical signaling factor for a variety of developmental pathways during embryogenesis, including the specification of left-right asymmetry in the heart. Mice that lack Hedgehog signaling show a delay in the induction of cardiomyogenesis, as indicated by a delayed expression of Nkx2-5. To further examine a role for Shh in cardiomyogenesis, clonal populations of P19 cells that stably express Shh, termed P19(Shh) cells, were isolated. In monolayer P19(Shh) ...
Known for P19 Cells | Hedgehog Signaling | Fluorescence Models | Shh Gli2 | Zinc Finger |
Myocyte Enhancer Factor 2C and Nkx2–5 Up-regulate Each Other's Expression and Initiate Cardiomyogenesis in P19 Cells*
[ PUBLICATION ]
The Nkx2-5 homeodomain protein plays a key role in cardiomyogenesis. Ectopic expression in frog and zebrafish embryos results in an enlarged myocardium; however, expression of Nkx2-5 in fibroblasts was not able to trigger the development of beating cardiac muscle. In order to examine the ability of Nkx2-5 to modulate endogenous cardiac specific gene expression in cells undergoing early stages of differentiation, P19 cell lines overexpressing Nkx2-5 were differentiated in the absence of ...
Known for P19 Cells | Myocyte Enhancer | Nkx2 5 | Mef2c Expression | Cardiac Muscle |
Wnt1 and Wnt3a are signaling factors known to play a role in the induction of myogenesis in the myotome of the differentiating somite. Both factors may transduce their signal by a conserved pathway that leads to transcriptional regulation by beta-catenin/Lef1. beta-Catenin and Lef1 are found in the myotome prior to MyoD expression. We have utilized the P19 cell system to study the mechanisms by which Wnt3a may activate MyoD expression and subsequent skeletal muscle development. We have ...
Known for P19 Cells | Skeletal Myogenesis | Myod Expression | Beta Catenin | Wnt3a Protein |
BACKGROUND: Understanding stem cell differentiation is essential for the future design of cell therapies. While retinoic acid (RA) is the most potent small molecule enhancer of skeletal myogenesis in stem cells, the stage and mechanism of its function has not yet been elucidated. Further, the intersection of RA with other signalling pathways that stimulate or inhibit myogenesis (such as Wnt and BMP4, respectively) is unknown. Thus, the purpose of this study is to examine the molecular ...
Known for Skeletal Muscle | Retinoic Acid | Stem Cells | Bone Morphogenetic Protein | Myod Expression |
A Splice Variant of the ITF-2 Transcript Encodes a Transcription Factor That Inhibits MyoD Activity (∗)
[ PUBLICATION ]
Proteins of the basic helix-loop-helix (bHLH) family are transcription factors that bind DNA containing the E box motif (CANNTG) found in the promoters of many muscle-specific genes. ITF-2 is a bHLH protein with widespread expression that is thought to form active heterodimers with MyoD, a muscle-specific bHLH transcription factor. We have isolated cDNAs derived from two alternatively spliced forms of mouse ITF-2, termed MITF-2A and -2B. These proteins differ in their N termini. Neither ...
Known for Myod Activity | Splice Variant | Transcription Factors | Molecular Dna | Amino Acid |
Gli2 and MEF2C activate each other's expression and function synergistically during cardiomyogenesis in vitro
[ PUBLICATION ]
The transcription factors Gli2 (glioma-associated factor 2), which is a transactivator of Sonic Hedgehog (Shh) signalling, and myocyte enhancer factor 2C (MEF2C) play important roles in the development of embryonic heart muscle and enhance cardiomyogenesis in stem cells. Although the physiological importance of Shh signalling and MEF2 factors in heart development is well known, the mechanistic understanding of their roles is unclear. Here, we demonstrate that Gli2 and MEF2C activated ...
Known for Cardiomyogenesis Stem Cells | Heart Development | Transcription Factors | Mef2c Gene | Sonic Hedgehog |
MAN1, an Inner Nuclear Membrane Protein That Shares the LEM Domain with Lamina-associated Polypeptide 2 and Emerin*
[ PUBLICATION ]
The "MAN antigens" are polypeptides recognized by autoantibodies from a patient with a collagen vascular disease and localized to the nuclear envelope. We now show that one of the human MAN antigens termed MAN1 is a 82.3-kDa protein with an amino-terminal domain followed by two hydrophobic segments and a carboxyl-terminal tail. The MAN1 gene contains seven protein-coding exons and is assigned to human chromosome 12q14. Its mRNA is approximately 5.5 kilobases and is detected in several ...
Known for Lem Domain | Membrane Protein | Messenger Sequence Homology | Polypeptide 2 | Man1 Nuclear |
The E2 Ubiquitin Conjugase Rad6 Is Required for the ArgR/Mcm1 Repression of ARG1 Transcription
[ PUBLICATION ]
Transcription of the Saccharomyces cerevisiae ARG1 gene is under the control of both positive and negative elements. Activation of the gene in minimal medium is induced by Gcn4. Repression occurs in the presence of arginine and requires the ArgR/Mcm1 complex that binds to two upstream arginine control (ARC) elements. With the recent finding that the E2 ubiquitin conjugase Rad6 modifies histone H2B, we examined the role of Rad6 in the regulation of ARG1 transcription. We find that Rad6 is ...
Known for Arg1 Transcription | Histone H2b | Rich Medium | Ubiquitin Protein | Argr Mcm1 |
The Tale of Two Domains Proteomics and Genomics Analysis of SMYD2, A New Histone Methyltransferase*
[ PUBLICATION ]
Very little is known about SET- and MYND-containing protein 2 (SMYD2), a member of the SMYD protein family. However, the interest in better understanding the roles of SMYD2 has grown because of recent reports indicating that SMYD2 methylates p53 and histone H3. In this study, we present a combined proteomics and genomics study of SMYD2 designed to elucidate its molecular roles. We report the cytosolic and nuclear interactome of SMYD2 using a combination of immunoprecipitation coupled ...
Known for Histone Methyltransferase | Interaction Smyd2 | H3k4 Methylation | Smyd Protein | Mynd Domain |
MyoD Directly Up-regulates Premyogenic Mesoderm Factors during Induction of Skeletal Myogenesis in Stem Cells*
[ PUBLICATION ]
Gain- and loss-of-function experiments have illustrated that the family of myogenic regulatory factors is necessary and sufficient for the formation of skeletal muscle. Furthermore, MyoD required cellular aggregation to induce myogenesis in P19 embryonal carcinoma stem cells. To determine the mechanism by which stem cells can be directed into skeletal muscle, a time course of P19 cell differentiation was examined in the presence and absence of exogenous MyoD. By quantitative PCR, the ...
Known for Stem Cells | Skeletal Myogenesis | Premyogenic Mesoderm | Development Muscle | Cell Differentiation |
Gli2 and Meox1 are transcription factors that are expressed in the developing somite and play roles in the commitment of cells to the skeletal muscle lineage. To further define their roles in regulating myogenesis, the function of wild type and dominant-negative forms of Gli2 and Meox1 were examined in the context of differentiating P19 stem cells. We found that Gli2 overexpression up-regulated transcript levels of Meox1 and, conversely, Meox1 overexpression resulted in the upregulation ...
Known for P19 Cells | Skeletal Myogenesis | Transcription Factors | Fluorescence Models | Muscle Lineage |
Ascl1/Mash1 Is a Novel Target of Gli2 during Gli2-Induced Neurogenesis in P19 EC Cells
[ PUBLICATION ]
The Sonic Hedgehog (Shh) signaling pathway is important for neurogenesis in vivo. Gli transcription factors, effector proteins of the Shh signaling pathway, have neurogenic properties in vivo, which are still poorly understood. To study the molecular basis of neurogenic properties of Gli2, we used a well-established embryonic stem cell model, the P19 embryonal carcinoma (EC) cell line, which can be induced to differentiate into neurons in the presence of retinoic acid (RA). We found ...
Known for P19 Cells | Transcription Factors | Signaling Pathway | Retinoic Acid | Sonic Hedgehog |
FOXC1 and FOXC2 are forkhead/winged-helix transcription factors expressed in paraxial mesoderm and somites. Emphasizing the importance of FOXC1/2 during embryonic development, double-knockout mice lacking the alleles for both Foxc1 and Foxc2 failed to form segmented somites and undergo myogenesis. The present study aims to determine upstream factors that regulate Foxc1/2 expression during the differentiation of P19 cells into skeletal muscle. Previous work had shown that ...
Known for P19 Cells | Skeletal Myogenesis | Wnt Signaling | Transcription Factors | Development Muscle |
Key People For P19 Cells
Ilona Sylvia Skerjanc:Expert Impact
Concepts for whichIlona Sylvia Skerjanchas direct influence:P19 cells, Skeletal myogenesis, Stem cells, Myod expression, Skeletal muscle, Transcription factors, Myod activity, Cardiac muscle.
Ilona Sylvia Skerjanc:KOL impact
Concepts related to the work of other authors for whichfor which Ilona Sylvia Skerjanc has influence:Stem cells, Skeletal muscle, Nuclear envelope, Transcription factors, Myogenic differentiation, Gene expression, Cell cycle.
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