ENU-induced phenovariance in mice: inferences from 587 mutations.
about
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencingMouse Genome Informatics (MGI): reflecting on 25 yearsCreating diseases to understand what prevents them: genetic analysis of inflammation in the gastrointestinal tractMutation of the ER retention receptor KDELR1 leads to cell-intrinsic lymphopenia and a failure to control chronic viral infectionCarcinogen-specific mutations in preferred Ras-Raf pathway oncogenes directed by strand bias.Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice.Dissecting mammalian immunity through mutation.An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouseThe Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease.Functional annotation and ENUMouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives.Real-time resolution of point mutations that cause phenovariance in mice.Quantitative reduction of the TCR adapter protein SLP-76 unbalances immunity and immune regulation.Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cells.Discovery and Structure-Activity Relationships of the Neoseptins: A New Class of Toll-like Receptor-4 (TLR4) Agonists.The International Mouse Strain Resource (IMSR): cataloging worldwide mouse and ES cell line resources.Going forward with genetics: recent technological advances and forward genetics in mice.Heterozygous mis-sense mutations in Prkcb as a critical determinant of anti-polysaccharide antibody formation.Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activity.Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice.A deep intronic mutation in the ankyrin-1 gene causes diminished protein expression resulting in hemolytic anemia in miceENU mutation mapped to a distal region of chromosome 11 is a major determinant of bone size.Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse.An ENU-induced splice site mutation of mouse Col1a1 causing recessive osteogenesis imperfecta and revealing a novel splicing rescueWhole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse
P2860
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P2860
ENU-induced phenovariance in mice: inferences from 587 mutations.
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
ENU-induced phenovariance in mice: inferences from 587 mutations.
@ast
ENU-induced phenovariance in mice: inferences from 587 mutations.
@en
ENU-induced phenovariance in mice: inferences from 587 mutations.
@nl
type
label
ENU-induced phenovariance in mice: inferences from 587 mutations.
@ast
ENU-induced phenovariance in mice: inferences from 587 mutations.
@en
ENU-induced phenovariance in mice: inferences from 587 mutations.
@nl
prefLabel
ENU-induced phenovariance in mice: inferences from 587 mutations.
@ast
ENU-induced phenovariance in mice: inferences from 587 mutations.
@en
ENU-induced phenovariance in mice: inferences from 587 mutations.
@nl
P2093
P2860
P50
P356
P1433
P1476
ENU-induced phenovariance in mice: inferences from 587 mutations.
@en
P2093
Amanda L Blasius
Anne R Murray
Carrie N Arnold
Celine Eidenschenk
Daniel L Popkin
Diantha La Vine
Eva Marie Y Moresco
Michael Berger
P2860
P2888
P356
10.1186/1756-0500-5-577
P50
P577
2012-10-24T00:00:00Z
P5875
P6179
1017825919