Search Results - "Imamoto, Akira"
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Cell shape‐based chemical screening reveals an epigenetic network mediated by focal adhesions
Published in The FEBS journal (01-10-2021)“…Adapter proteins CRK and CRKL participate in a variety of signaling pathways, including cell adhesion, and fate regulation of mammalian cells. However, the…”
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2
Dose-Dependent Interaction of Tbx1 and Crkl and Locally Aberrant RA Signaling in a Model of del22q11 Syndrome
Published in Developmental cell (2006)“…22q11 deletion ( del22q11) syndrome is characterized genetically by heterozygous deletions within chromosome 22q11 and clinically by a constellation of…”
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3
Activation of a Dab1/CrkL/C3G/Rap1 Pathway in Reelin-Stimulated Neurons
Published in Current biology (06-04-2004)“…During brain development, many neurons migrate long distances before settling and differentiating. These migrations are coordinated to ensure normal…”
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4
A pre-metazoan origin of the CRK gene family and co-opted signaling network
Published in Scientific reports (30-09-2016)“…CRK and CRKL adapter proteins play essential roles in development and cancer through their SRC homology 2 and 3 (SH2 and SH3) domains. To gain insight into the…”
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5
The Adaptor Protein Paxillin Is Essential for Normal Development in the Mouse and Is a Critical Transducer of Fibronectin Signaling
Published in Molecular and Cellular Biology (01-02-2002)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Crkl Deficiency Disrupts Fgf8 Signaling in a Mouse Model of 22q11 Deletion Syndromes
Published in Developmental cell (2006)“…Deletions on chromosome 22q11.21 disrupt pharyngeal and cardiac development and cause DiGeorge and related human syndromes. CRKL ( CRK-Like) lies within…”
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7
Structural and Functional Basis of a Role for CRKL in a Fibroblast Growth Factor 8-Induced Feed-Forward Loop
Published in Molecular and Cellular Biology (01-06-2009)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome
Published in Nature genetics (01-03-2001)“…Heterozygous deletions within human chromosome 22q11 are the genetic basis of DiGeorge/velocardiofacial syndrome (DGS/VCFS), the most common deletion syndrome…”
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Disruption of Overlapping Transcripts in the ROSA β geo 26 Gene Trap Strain Leads to Widespread Expression of β -Galactosidase in Mouse Embryos and Hematopoietic Cells
Published in Proceedings of the National Academy of Sciences - PNAS (15-04-1997)“…The ROSAβ geo26 (ROSA26) mouse strain was produced by random retroviral gene trapping in embryonic stem cells. Staining of ROSA26 tissues and…”
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Focal Adhesions Require Catalytic Activity of Src Family Kinases To Mediate Integrin-Matrix Adhesion
Published in Molecular and Cellular Biology (01-02-2002)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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11
Raf Kinase Inhibitory Protein protects cells against locostatin-mediated inhibition of migration
Published in PloS one (24-06-2009)“…Raf Kinase Inhibitory Protein (RKIP, also PEBP1), a member of the Phosphatidylethanolamine Binding Protein family, negatively regulates growth factor signaling…”
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Disruption of the csk gene, encoding a negative regulator of Src family tyrosine kinases, leads to neural tube defects and embryonic lethality in mice
Published in Cell (18-06-1993)“…All Src family non-receptor tyrosine kinases are negatively regulated by phosphorylation at a carboxy-terminal tyrosine. To analyze the significance of this…”
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13
Translocation of CrkL to Focal Adhesions Mediates Integrin-Induced Migration Downstream of Src Family Kinases
Published in Molecular and Cellular Biology (01-04-2003)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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14
A Specific Need for CRKL in p210BCR-ABL―Induced Transformation of Mouse Hematopoietic Progenitors
Published in Cancer research (Chicago, Ill.) (15-09-2010)“…CRKL (CRK-like) is an adapter protein predominantly phosphorylated in cells that express the tyrosine kinase p210(BCR-ABL), the fusion product of a (9;22)…”
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15
COOH-terminal src kinase-mediated c-jun phosphorylation promotes c-jun degradation and inhibits cell transformation
Published in Cancer research (Chicago, Ill.) (01-06-2006)“…The oncoprotein c-Jun is a component of the activator protein-1 transcription factor complex, which is involved in cellular proliferation, transformation, and…”
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Dual roles of the C-terminal Src kinase (Csk) during developmental vascularization
Published in Blood (15-02-2004)“…Here we report that C-terminal Src kinase (Csk), a tyrosine kinase that negatively regulates the activity of Src and related kinases, is important for vascular…”
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Murine model indicates 22q11.2 signaling adaptor CRKL is a dosage-sensitive regulator of genitourinary development
Published in Proceedings of the National Academy of Sciences - PNAS (09-05-2017)“…The spectrum of congenital anomalies affecting either the upper tract (kidneys and ureters) or lower tract (reproductive organs) of the genitourinary (GU)…”
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18
Colony-stimulating factor-1 receptor utilizes multiple signaling pathways to induce cyclin D2 expression
Published in Molecular biology of the cell (01-11-2000)“…Colony-stimulating factor-1 (CSF-1) induces expression of immediate early gene, such as c-myc and c-fos and delayed early genes such as D-type cyclins (D1 and…”
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Raf kinase inhibitory protein (RKIP): a physiological regulator and future therapeutic target
Published in Expert opinion on therapeutic targets (01-10-2008)“…Raf kinase inhibitory protein (RKIP) belongs to the phosphatidylethanolamine binding protein (PEBP) family that is expressed in both prokaryotic and…”
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Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
Published in The New England journal of medicine (23-02-2017)“…A third of patients with the DiGeorge syndrome have congenital kidney and urinary tract anomalies. This study provides evidence that haploinsufficiency of CRKL…”
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