Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos - Wikidata - awgldk - TriplyDB

Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos

Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos

http://www.wikidata.org/entity/Q35206785

about

Cdx2 is essential for axial elongation in mouse development FGF signalling: diverse roles during early vertebrate embryogenesis Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies Additive effects of PDGF receptor beta signaling pathways in vascular smooth muscle cell development Genetic insights into the mechanisms of Fgf signaling Evidence-Based Theory for Integrated Genome Regulation of Ontogeny--An Unprecedented Role of Nuclear FGFR1 Signaling Receptor tyrosine kinase signaling: regulating neural crest development one phosphate at a time Signaling by FGF4 and FGF8 is required for axial elongation of the mouse embryo Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model Targeted mutations of the juxtamembrane tyrosines in the Kit receptor tyrosine kinase selectively affect multiple cell lineages FGFR1 is independently required in both developing mid- and hindbrain for sustained response to isthmic signals Signals and switches in Mammalian neural crest cell differentiation Breaking evolutionary and pleiotropic constraints in mammals: On sloths, manatees and homeotic mutations Expression of ERK signaling inhibitors Dusp6, Dusp7, and Dusp9 during mouse ear development.Fibroblast growth factor (FGF) receptor 1-IIIb is a naturally occurring functional receptor for FGFs that is preferentially expressed in the skin and the brain.Frs2α and Shp2 signal independently of Gab to mediate FGF signaling in lens development.Fibroblast growth factor deficiencies impact anxiety-like behavior and the serotonergic system.Signaling gradients during paraxial mesoderm development.Fibroblast growth factor 9 signaling inhibits airway smooth muscle differentiation in mouse lung Fibroblast growth factor (FGF) signaling through PI 3-kinase and Akt/PKB is required for embryoid body differentiation.A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice.Deletion of Fgfr1 in osteoblasts enhances mobilization of EPCs into peripheral blood in a mouse endotoxemia model LoxP-FRT Trap (LOFT): a simple and flexible system for conventional and reversible gene targeting HOX deregulation in acute myeloid leukemia A method for the generation of conditional gene repair mutations in mice Three-dimensional culture and FGF signaling drive differentiation of murine pluripotent cells to distal lung epithelial cells.FGFs, their receptors, and human limb malformations: clinical and molecular correlations.Compound deficiencies in multiple fibroblast growth factor signalling components differentially impact the murine gonadotrophin-releasing hormone system Concordia discors: duality in the origin of the vertebrate tail.Global Developmental Gene Programing Involves a Nuclear Form of Fibroblast Growth Factor Receptor-1 (FGFR1).FGF2 posttranscriptionally down-regulates expression of SDF1 in bone marrow stromal cells through FGFR1 IIIc.Distinct sets of FGF receptors sculpt excitatory and inhibitory synaptogenesis.Platelet-derived growth factor beta receptor regulates interstitial fluid homeostasis through phosphatidylinositol-3' kinase signaling Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3.Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome Role of FGF/FGFR signaling in skeletal development and homeostasis: learning from mouse models.Fibroblast growth factor signaling deficiencies impact female reproduction and kisspeptin neurons in mice A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1 Fgfr1 regulates development through the combinatorial use of signaling proteins.Signaling networks that control the lineage commitment and differentiation of bone cells.

P2860

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P2860

Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos

http://www.wikidata.org/entity/Q35206785

description

1998 nî lūn-bûn

@nan

1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի օգոստոսին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年论文

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name

Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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Opposite phenotypes of hypomor ...... or patterning of mouse embryos

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J Partanen

http://www.w3.org/2001/XMLSchema#string

J Rossant

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L Schwartz

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P2860

The human fibroblast growth factor receptor genes: a common structural arrangement underlies the mechanisms for generating receptor forms that differ in their third immunoglobulin domain

Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern

Receptor specificity of the fibroblast growth factor family

Homeosis and intestinal tumours in Cdx2 mutant mice

Fibroblast growth factor receptor-4 shows novel features in genomic structure, ligand binding and signal transduction

Molecular models for vertebrate limb development

A mutational analysis of the 5' HoxD genes: dissection of genetic interactions during limb development in the mouse

Point mutation in the fibroblast growth factor receptor eliminates phosphatidylinositol hydrolysis without affecting neuronal differentiation of PC12 cells

Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos

Fibroblast growth factor receptor 2 (FGFR2)-mediated reciprocal regulation loop between FGF8 and FGF10 is essential for limb induction

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15

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phosphorylation

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