Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
about
A widespread peroxiredoxin-like domain present in tumor suppression- and progression-implicated proteinsSRPX2 is a novel chondroitin sulfate proteoglycan that is overexpressed in gastrointestinal cancerPCSK6 is associated with handedness in individuals with dyslexiaXLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencingVEGF-initiated angiogenesis and the uPA/uPAR systemRecent Advances in the Genetics of Vocal LearningGlobularity and language-readiness: generating new predictions by expanding the set of genes of interestProfiling trait anxiety: transcriptome analysis reveals cathepsin B (Ctsb) as a novel candidate gene for emotionality in miceMolecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex.SRPX2 promotes cell migration and invasion via FAK dependent pathway in pancreatic cancer.Identification of steroid-sensitive gene-1/Ccdc80 as a JAK2-binding protein.A molecular classification of human mesenchymal stromal cells.Extracellular matrix in plasticity and epileptogenesis.New differentially expressed genes and differential DNA methylation underlying refractory epilepsy."Electro-clinical syndromes" with onset in paediatric age: the highlights of the clinical-EEG, genetic and therapeutic advances.Genetics, molecular biology, and phenotypes of x-linked epilepsy.Single-Gene Determinants of Epilepsy Comorbidity.Non-CpG island promoter hypomethylation and miR-149 regulate the expression of SRPX2 in colorectal cancer.Urokinase-type plasminogen activator receptor modulates epileptogenesis in mouse model of temporal lobe epilepsy.Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome.Molecular Fingerprint for Terminal Abdominal Aortic Aneurysm Disease.SRPX2 regulates colon cancer cell metabolism by miR-192/215 via PI3K-Akt.Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.Increased Sushi repeat-containing protein X-linked 2 is associated with progression of colorectal cancer.High SRPX2 protein expression predicts unfavorable clinical outcome in patients with prostate cancer.Toward the Language Oscillogenome
P2860
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P2860
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Epileptic and developmental di ...... inogen activator receptor uPAR
@ast
Epileptic and developmental di ...... inogen activator receptor uPAR
@en
Epileptic and developmental di ...... inogen activator receptor uPAR
@en-gb
Epileptic and developmental di ...... inogen activator receptor uPAR
@nl
type
label
Epileptic and developmental di ...... inogen activator receptor uPAR
@ast
Epileptic and developmental di ...... inogen activator receptor uPAR
@en
Epileptic and developmental di ...... inogen activator receptor uPAR
@en-gb
Epileptic and developmental di ...... inogen activator receptor uPAR
@nl
prefLabel
Epileptic and developmental di ...... inogen activator receptor uPAR
@ast
Epileptic and developmental di ...... inogen activator receptor uPAR
@en
Epileptic and developmental di ...... inogen activator receptor uPAR
@en-gb
Epileptic and developmental di ...... inogen activator receptor uPAR
@nl
P2093
P50
P3181
P356
P1476
Epileptic and developmental di ...... inogen activator receptor uPAR
@en
P2093
Barbara Royer-Zemmour
Christian Lévêque
Géraldine Ferracci
Jennifer Cillario
Magali Ponsole-Lenfant
Patrice Roll
Renaud Vincentelli
P304
P3181
P356
10.1093/HMG/DDN256
P407
P577
2008-12-01T00:00:00Z