Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development - Test2 - elhamkhani - TriplyDB

Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

http://www.wikidata.org/entity/Q27323992

about

The bigger the better: determining nephron size in kidney A critical role for NF2 and the Hippo pathway in branching morphogenesis Cdc42 is required for cytoskeletal support of endothelial cell adhesion during blood vessel formation in mice.Development of the Mammalian Kidney Relationship of and cross-talk between physical and biologic properties of the glomerulus Concise Review: Understanding the Renal Progenitor Cell Niche In Vivo to Recapitulate Nephrogenesis In Vitro Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer Multiparametric Analysis of Cell Shape Demonstrates that β-PIX Directly Couples YAP Activation to Extracellular Matrix Adhesion YAP and TAZ control peripheral myelination and the expression of laminin receptors in Schwann cells The Hippo pathway effector YAP is an essential regulator of ductal progenitor patterning in the mouse submandibular gland.Induction and patterning of the metanephric nephron Signaling by the engulfment receptor draper: a screen in Drosophila melanogaster implicates cytoskeletal regulators, Jun N-terminal Kinase, and Yorkie.Non-canonical roles for Yorkie and Drosophila Inhibitor of Apoptosis 1 in epithelial tube size control Disease implications of the Hippo/YAP pathway.BMP9 Crosstalk with the Hippo Pathway Regulates Endothelial Cell Matricellular and Chemokine Responses.A conserved MST1/2-YAP axis mediates Hippo signaling during lung growth.Yap and Taz are required for Ret-dependent urinary tract morphogenesis FAT1 mutations cause a glomerulotubular nephropathy Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.Genome-Wide Analysis of Wilms' Tumor 1-Controlled Gene Expression in Podocytes Reveals Key Regulatory Mechanisms The emerging roles of YAP and TAZ in cancer RhoA deficiency disrupts podocyte cytoskeleton and induces podocyte apoptosis by inhibiting YAP/dendrin signal Rho GTPases in embryonic development Pals1 Haploinsufficiency Results in Proteinuria and Cyst Formation.Cdc42 regulates epithelial cell polarity and cytoskeletal function during kidney tubule development.Yap is required for ependymal integrity and is suppressed in LPA-induced hydrocephalus Cdc42 deficiency induces podocyte apoptosis by inhibiting the Nwasp/stress fibers/YAP pathway.Cysteine S-Glutathionylation Promotes Stability and Activation of the Hippo Downstream Effector Transcriptional Co-activator with PDZ-binding Motif (TAZ).Interaction of the EGF Receptor and the Hippo Pathway in the Diabetic Kidney.The Hippo-Salvador signaling pathway regulates renal tubulointerstitial fibrosis.Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development.Regulation of the Hippo pathway and implications for anticancer drug development.Aberrant activation, nuclear localization, and phosphorylation of Yes-associated protein-1 in the embryonic kidney and Wilms tumor.Amotl1 mediates sequestration of the Hippo effector Yap1 downstream of Fat4 to restrict heart growth.The Hippo signaling pathway provides novel anti-cancer drug targets.Systematic morphological profiling of human gene and allele function via Cell Painting.Hippo gains weight: added insights and complexity to pathway control.The mammalian Hippo pathway: regulation and function of YAP1 and TAZ.Hippo signaling in stress response and homeostasis maintenance.Stressed podocytes-mechanical forces, sensors, signaling and response.

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

http://www.wikidata.org/entity/Q27323992

description

2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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JOURNAL.PGEN.1003380

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

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Alex Gregorieff

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Antoine Reginensi

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Chaeuk Chung

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Helen McNeill

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P2860

Regulation of the Hippo-YAP pathway by G-protein-coupled receptor signaling

The Hippo pathway regulates Wnt/beta-catenin signaling

Calpain 6 is involved in microtubule stabilization and cytoskeletal organization

The hippo signaling pathway in development and cancer

Rho GTPases: biochemistry and biology

Wnt/beta-catenin signaling regulates nephron induction during mouse kidney development

Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size

The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation

The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass

A crucial role of WW45 in developing epithelial tissues in the mouse

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