scholarly article | Q13442814 |
P2093 | author name string | Hong Zhang | |
Ed Stavnezer | |||
P2860 | cites work | Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor | Q22008813 |
The Ski protein family is required for MeCP2-mediated transcriptional repression | Q24291417 | ||
Fussel-15, a novel Ski/Sno homolog protein, antagonizes BMP signaling | Q24296714 | ||
SKI activates Wnt/beta-catenin signaling in human melanoma | Q24298640 | ||
Interaction with Smad4 is indispensable for suppression of BMP signaling by c-Ski | Q24303530 | ||
The Ski oncoprotein interacts with Skip, the human homolog of Drosophila Bx42 | Q24311912 | ||
Cloning and functional characterization of a new Ski homolog, Fussel-18, specifically expressed in neuronal tissues | Q24337448 | ||
Molecular interaction and synergistic activation of a promoter by Six, Eya, and Dach proteins mediated through CREB binding protein | Q24537783 | ||
Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya | Q24554423 | ||
Ski interacts with the evolutionarily conserved SNW domain of Skip | Q24555232 | ||
Tight control of gene expression in mammalian cells by tetracycline-responsive promoters | Q24564850 | ||
Combinatorial control of muscle development by basic helix-loop-helix and MADS-box transcription factors | Q24594377 | ||
The Ski oncoprotein interacts with the Smad proteins to repress TGFbeta signaling | Q24599753 | ||
SnoI, a novel alternatively spliced isoform of the ski protooncogene homolog, sno. | Q24617524 | ||
A new myocyte-specific enhancer-binding factor that recognizes a conserved element associated with multiple muscle-specific genes | Q24631256 | ||
Isolation of human cDNA clones of ski and the ski-related gene, sno | Q24635631 | ||
c-Ski acts as a transcriptional co-repressor in transforming growth factor-beta signaling through interaction with smads | Q28138749 | ||
Molecular mechanisms regulating myogenic determination and differentiation | Q28145088 | ||
Interaction of the Ski oncoprotein with Smad3 regulates TGF-beta signaling | Q28146183 | ||
Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis | Q28185761 | ||
Altered myogenesis in Six1-deficient mice | Q28187781 | ||
Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins | Q28214522 | ||
Myogenin resides in the nucleus and acquires high affinity for a conserved enhancer element on heterodimerization | Q28239333 | ||
The eye-specification proteins So and Eya form a complex and regulate multiple steps in Drosophila eye development | Q28258959 | ||
Crystal structure of the dachshund homology domain of human SKI | Q28260495 | ||
Probing tumor phenotypes using stable and regulated synthetic microRNA precursors | Q28275174 | ||
Second-generation shRNA libraries covering the mouse and human genomes | Q28275183 | ||
Mammalian and Drosophila dachshund genes are related to the Ski proto-oncogene and are expressed in eye and limb | Q28275505 | ||
Human SRF-related proteins: DNA-binding properties and potential regulatory targets | Q28300739 | ||
Activation of a muscle-specific enhancer by the Ski proto-oncogene | Q28505793 | ||
Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development | Q28507155 | ||
Corl1, a novel neuronal lineage-specific transcriptional corepressor for the homeodomain transcription factor Lbx1 | Q28508618 | ||
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice | Q28510846 | ||
c-Ski activates MyoD in the nucleus of myoblastic cells through suppression of histone deacetylases | Q28589107 | ||
Tissue-specific regulation of retinal and pituitary precursor cell proliferation | Q28589859 | ||
Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site | Q28589912 | ||
ski can cause selective growth of skeletal muscle in transgenic mice | Q68624469 | ||
A carboxyl-terminal region of the ski oncoprotein mediates homodimerization as well as heterodimerization with the related protein SnoN | Q72724829 | ||
Dedifferentiation of mammalian myotubes induced by msx1 | Q73406479 | ||
Thymus, kidney and craniofacial abnormalities in Six 1 deficient mice | Q73593261 | ||
Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila | Q74037490 | ||
Viral ski inhibits retinoblastoma protein (Rb)-mediated transcriptional repression in a dominant negative fashion | Q78168212 | ||
Differences and similarities in DNA-binding preferences of MyoD and E2A protein complexes revealed by binding site selection | Q29617433 | ||
Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation | Q33885274 | ||
A lentiviral microRNA-based system for single-copy polymerase II-regulated RNA interference in mammalian cells | Q33938488 | ||
Six family genes--structure and function as transcription factors and their roles in development | Q33957333 | ||
Mechanisms underlying the transcriptional regulation of skeletal myogenesis. | Q34131477 | ||
Ski/Sno and TGF-beta signaling. | Q34225107 | ||
Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode | Q34414173 | ||
MyoD and the transcriptional control of myogenesis | Q34442774 | ||
Myogenic regulatory factors and the specification of muscle progenitors in vertebrate embryos | Q34762477 | ||
Activation of the myogenin promoter during mouse embryogenesis in the absence of positive autoregulation | Q34779892 | ||
Generation of transforming viruses in cultures of chicken fibroblasts infected with an avian leukosis virus | Q35241487 | ||
Ski acts as a co-repressor with Smad2 and Smad3 to regulate the response to type beta transforming growth factor | Q35754725 | ||
Requirement of protein co-factor for the DNA-binding function of the human ski proto-oncogene product | Q35827450 | ||
Transformation of hematopoietic cells by the Ski oncoprotein involves repression of retinoic acid receptor signaling | Q36308232 | ||
Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis. | Q36382342 | ||
Transformation-defective v-ski induces MyoD and myogenin expression but not myotube formation | Q36685768 | ||
Analysis of the myogenin promoter reveals an indirect pathway for positive autoregulation mediated by the muscle-specific enhancer factor MEF-2 | Q36698404 | ||
Activation of the c-ski oncogene by overexpression | Q36797799 | ||
Unique sequence, ski, in Sloan-Kettering avian retroviruses with properties of a new cell-derived oncogene | Q36859974 | ||
Transforming Sloan-Kettering viruses generated from the cloned v-ski oncogene by in vitro and in vivo recombinations | Q36859994 | ||
Skeletal muscle satellite cells and adult myogenesis. | Q36998129 | ||
The emerging biology of satellite cells and their therapeutic potential | Q37064632 | ||
Paired MyoD-binding sites regulate myosin light chain gene expression | Q37399134 | ||
Structure and activities of the ski oncogene | Q37805045 | ||
Binding of C/EBPbeta to the C-reactive protein (CRP) promoter in Hep3B cells is associated with transcription of CRP mRNA. | Q39953275 | ||
Regulation of Muscle Differentiation by the MEF2 Family of MADS Box Transcription Factors | Q40432858 | ||
A highly conserved enhancer downstream of the human MLC1/3 locus is a target for multiple myogenic determination factors | Q40525469 | ||
Repression of endogenous Smad7 by Ski. | Q40558828 | ||
Trans-regulation of myogenin promoter/enhancer activity by c-ski during skeletal-muscle differentiation: the C-terminus of the c-Ski protein is essential for transcriptional regulatory activity in myotubes | Q41070504 | ||
Enhanced expression of mouse c-ski accompanies terminal skeletal muscle differentiation in vivo and in vitro | Q41275887 | ||
Determinants of myogenic specificity within MyoD are required for noncanonical E box binding | Q42412056 | ||
Identification of a new class of PAX3-FKHR target promoters: a role of the Pax3 paired box DNA binding domain | Q42703157 | ||
Pbx marks genes for activation by MyoD indicating a role for a homeodomain protein in establishing myogenic potential | Q42828894 | ||
Oxidative stress is the new stress | Q46839696 | ||
Mouse Dach, a homologue of Drosophila dachshund, is expressed in the developing retina, brain and limbs | Q47925213 | ||
Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development. | Q48068853 | ||
The regulation of myogenin gene expression during the embryonic development of the mouse | Q48112077 | ||
The Msh-like homeobox genes define domains in the developing vertebrate eye. | Q48217316 | ||
The ski oncogene induces muscle differentiation in quail embryo cells. | Q51173935 | ||
Identification of a core functional and structural domain of the v-Ski oncoprotein responsible for both transformation and myogenesis. | Q53441456 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
myotube differentiation | Q14762267 | ||
SKI proto-oncogene | Q14913250 | ||
EYA transcriptional coactivator and phosphatase 3 | Q21981870 | ||
Sine oculis-related homeobox 1 | Q21981883 | ||
Ski oncogene | Q21990617 | ||
P304 | page(s) | 2867-79 | |
P577 | publication date | 2009-01-30 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Ski regulates muscle terminal differentiation by transcriptional activation of Myog in a complex with Six1 and Eya3 | |
P478 | volume | 284 |
Q33530166 | Characterization of microRNAs from sheep (Ovis aries) using computational and experimental analyses |
Q35009781 | Characterization of the functional role of nucleotides within the URE2 IRES element and the requirements for eIF2A-mediated repression |
Q30502592 | Chromosomal instability in mouse embryonic fibroblasts null for the transcriptional co-repressor Ski. |
Q35207442 | Excitation‐transcription coupling in skeletal muscle: the molecular pathways of exercise |
Q39188632 | Expression of Ski can act as a negative feedback mechanism on retinoic acid signaling. |
Q33883339 | Kruppel-like factor 4 inhibits epithelial-to-mesenchymal transition through regulation of E-cadherin gene expression |
Q35639937 | Mitogen-activated protein kinase extracellular signal-regulated kinase 2 phosphorylates and promotes Pin1 protein-dependent promyelocytic leukemia protein turnover |
Q39256753 | Overexpression of Six1 leads to retardation of myogenic differentiation in C2C12 myoblasts |
Q35562803 | Peroxisome proliferator-activated receptor γ (PPARγ) mediates a Ski oncogene-induced shift from glycolysis to oxidative energy metabolism |
Q33744538 | Promyelocytic leukemia protein controls cell migration in response to hydrogen peroxide and insulin-like growth factor-1 |
Q84759300 | SKI knockdown inhibits human melanoma tumor growth in vivo |
Q28589792 | Six family genes control the proliferation and differentiation of muscle satellite cells |
Q84381185 | Six1 and Six1 cofactor expression is altered during early skeletal muscle overload in mice |
Q38184513 | Six1: a critical transcription factor in tumorigenesis |
Q33569692 | The Notch effector Hey1 associates with myogenic target genes to repress myogenesis. |
Q38248282 | The role of Six1 in the genesis of muscle cell and skeletal muscle development |
Q40637660 | Time course and side-by-side analysis of mesodermal, pre-myogenic, myogenic and differentiated cell markers in the chicken model for skeletal muscle formation |
Q38337450 | Transcriptional analysis of the titin cap gene |
Q62060038 | Transcriptional cofactors Ski and SnoN are major regulators of the TGF-β/Smad signaling pathway in health and disease |
Q37885788 | c-Ski in health and disease |
Q90577000 | miR-23a-3p/SIX1 regulates glucose uptake and proliferation through GLUT3 in head and neck squamous cell carcinomas |
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