Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.
about
MEGF8 is a modifier of BMP signaling in trigeminal sensory neuronsMutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralizationComparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxiaDisruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromeGenome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseMicrotubule actin crosslinking factor 1 regulates the Balbiani body and animal-vegetal polarity of the zebrafish oocyte.Inflammation aggravates disease severity in Marfan syndrome patients.Large-scale identification of chemically induced mutations in Drosophila melanogaster.Discovery Genetics - The History and Future of Spontaneous Mutation Research.Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.Real-time resolution of point mutations that cause phenovariance in mice.Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.Mutation discovery in mice by whole exome sequencing.Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of disease.Complex Network Clustering by a Multi-objective Evolutionary Algorithm Based on Decomposition and Membrane Structure.Ex vivo method for high resolution imaging of cilia motility in rodent airway epithelia.Genetic Modifier Screens in Mice.Genetic basis of human left-right asymmetry disorders.Axitinib and sorafenib are potent in tyrosine kinase inhibitor resistant chronic myeloid leukemia cellsCRISPR Screens Uncover Genes that Regulate Target Cell Sensitivity to the Morphogen Sonic Hedgehog.Organ Dynamics and Fluid Dynamics of the HH25 Chick Embryonic Cardiac Ventricle as Revealed by a Novel 4D High-Frequency Ultrasound Imaging Technique and Computational Flow Simulations.The Drosophila homologue of MEGF8 is essential for early development.
P2860
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P2860
Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Massively parallel sequencing ...... ed mutation causing heterotaxy
@nl
Massively parallel sequencing ...... d mutation causing heterotaxy.
@ast
Massively parallel sequencing ...... d mutation causing heterotaxy.
@en
type
label
Massively parallel sequencing ...... ed mutation causing heterotaxy
@nl
Massively parallel sequencing ...... d mutation causing heterotaxy.
@ast
Massively parallel sequencing ...... d mutation causing heterotaxy.
@en
prefLabel
Massively parallel sequencing ...... ed mutation causing heterotaxy
@nl
Massively parallel sequencing ...... d mutation causing heterotaxy.
@ast
Massively parallel sequencing ...... d mutation causing heterotaxy.
@en
P2093
P2860
P50
P356
P1476
Massively parallel sequencing ...... d mutation causing heterotaxy.
@en
P2093
Bishwanath Chatterjee
Cecilia W Lo
Deanne Alpert
Joel Martin
Kenneth L Kramer
Len A Pennacchio
Maxim Koriabine
Pieter J De Jong
P2860
P304
P356
10.1073/PNAS.0813400106
P407
P577
2009-02-13T00:00:00Z