A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3. - Wikidata - wikimedia - TriplyDB

A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3.

A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3.

http://www.wikidata.org/entity/Q34982454

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Repulsive axon guidance molecule Slit3 is a novel angiogenic factor Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population Slit-Robo interactions during cortical development New Insights into Congenital Diaphragmatic Hernia - A Surgeon's Introduction to CDH Animal Models.Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia.The gene expression signatures of melanoma progression Genetic aspects of human congenital diaphragmatic hernia.Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm.Axon guidance and synaptic maintenance: preclinical markers for neurodegenerative disease and therapeutics Involvement of the SLIT/ROBO pathway in follicle development in the fetal ovary.Expression of Slit and Robo genes in the developing mouse heart.Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3.Teratogen-induced, dietary and genetic models of congenital diaphragmatic hernia share a common mechanism of pathogenesis.Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.Genetic factors in congenital diaphragmatic hernia.Expression and roles of Slit/Robo in human ovarian cancer.Coup d'Etat: an orphan takes control.The C-terminal fragment of axon guidance molecule Slit3 binds heparin and neutralizes heparin's anticoagulant activity.Wt1 and β-catenin cooperatively regulate diaphragm development in the mouse.Expression patterns of Slit and Robo family members in adult mouse spinal cord and peripheral nervous system.Molecular genetics of congenital diaphragmatic defects.Non-contact respiration monitoring for in-vivo murine micro computed tomography: characterization and imaging applications Roundabout receptors are critical for foregut separation from the body wall.Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.Pleural and pericardial effusion: a potential ultrasonographic marker for the prenatal differential diagnosis between congenital diaphragmatic eventration and congenital diaphragmatic hernia.Linking animal models to human congenital diaphragmatic hernia.Kif7 is required for the patterning and differentiation of the diaphragm in a model of syndromic congenital diaphragmatic hernia.Slit/Robo signaling mediates spatial positioning of spiral ganglion neurons during development of cochlear innervation.Characterization of the interaction between Robo1 and heparin and other glycosaminoglycans.Heparan sulfate deficiency disrupts developmental angiogenesis and causes congenital diaphragmatic hernia.Robo1 modulates proliferation and neurogenesis in the developing neocortex.Epigenetic inactivation of SLIT3 and SLIT1 genes in human cancers.A systems biology approach to defining regulatory mechanisms for cartilage and tendon cell phenotypes.Congenital diaphragmatic hernias: from genes to mechanisms to therapies.Concurrent congenital peritoneopericardial diaphragmatic hernia and bochdalek hernia in a neonate Robo-2 controls the segregation of a portion of basal vomeronasal sensory neuron axons to the posterior region of the accessory olfactory bulb.Computer simulation analysis of normal and abnormal development of the mammalian diaphragm.Autocrine/juxtaparacrine regulation of axon fasciculation by Slit-Robo signaling.Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

P2860

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P2860

A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3.

http://www.wikidata.org/entity/Q34982454

description

2003 nî lūn-bûn

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2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2003 թվականի ապրիլին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central

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A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central

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A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central ...... hernia in mice lacking Slit3.

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A genetic model for a central

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A genetic model for a central ...... c hernia in mice lacking Slit3

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Jane Y Wu

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John J Greer

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Randal P Babiuk

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Wenlin Yuan

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Yi Rao

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P2860

Cloning and expressions of three mammalian homologues of Drosophila slit suggest possible roles for Slit in the formation and maintenance of the nervous system

Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance

The neuronal repellent Slit inhibits leukocyte chemotaxis induced by chemotactic factors

Dual trafficking of Slit3 to mitochondria and cell surface demonstrates novel localization for Slit protein

Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors

Directional guidance of neuronal migration in the olfactory system by the protein Slit

Cloning and functional studies of a novel gene aberrantly expressed in RB-deficient embryos

Biochemical purification of a mammalian slit protein as a positive regulator of sensory axon elongation and branching

Vertebrate slit, a secreted ligand for the transmembrane protein roundabout, is a repellent for olfactory bulb axons

Repulsive axon guidance: Abelson and Enabled play opposing roles downstream of the roundabout receptor

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congenital diaphragmatic hernia

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154325

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