A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice.
about
The mouse genetics toolkit: revealing function and mechanismIncreased insulin action in SKIP heterozygous knockout miceAbnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismInduced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Modeling partial monosomy for human chromosome 21q11.2-q21.1 reveals haploinsufficient genes influencing behavior and fat depositionEngineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applicationsInsertional mutagenesis in mice: new perspectives and toolsCharacterization of PTZ-induced seizure susceptibility in a down syndrome mouse model that overexpresses CSTBUrocortin-deficient mice display normal stress-induced anxiety behavior and autonomic control but an impaired acoustic startle responseCOP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblastGenetic ablation of Rhbg in the mouse does not impair renal ammonium excretionSdmg1 is a conserved transmembrane protein associated with germ cell sex determination and germline-soma interactions in miceA mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions.Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice.Mutagenic insertion and chromosome engineering resource (MICER).Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains.Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organizationTransplantation of human embryonic stem cell-derived alveolar epithelial type II cells abrogates acute lung injury in mice.Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15.TAp63 induces senescence and suppresses tumorigenesis in vivo.Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic BehaviorControlled somatic and germline copy number variation in the mouse modelA deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromesModeling of the human alveolar rhabdomyosarcoma Pax3-Foxo1 chromosome translocation in mouse myoblasts using CRISPR-Cas9 nuclease.Genetic Models in Applied Physiology. Functional genomics in the mouse: powerful techniques for unraveling the basis of human development and disease.Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.A pure population of lung alveolar epithelial type II cells derived from human embryonic stem cells.Induced mitotic recombination of p53 in vivoDuplication of GTF2I results in separation anxiety in mice and humans.Generation of the Sotos syndrome deletion in mice.Mouse chromosome engineering for modeling human disease.Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient miceEffects of Feeder Cell Types on Culture of Mouse Embryonic Stem Cell In Vitro.Contemporary approaches for modifying the mouse genomeInducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombinationRapid generation of nested chromosomal deletions on mouse chromosome 2.The alpha/beta carboxy-terminal domains of p63 are required for skin and limb development. New insights from the Brdm2 mouse which is not a complete p63 knockout but expresses p63 gamma-like proteinsA new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome
P2860
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P2860
A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
A system for rapid generation ...... osomal rearrangements in mice.
@ast
A system for rapid generation ...... osomal rearrangements in mice.
@en
type
label
A system for rapid generation ...... osomal rearrangements in mice.
@ast
A system for rapid generation ...... osomal rearrangements in mice.
@en
prefLabel
A system for rapid generation ...... osomal rearrangements in mice.
@ast
A system for rapid generation ...... osomal rearrangements in mice.
@en
P2093
P2860
P356
P1476
A system for rapid generation ...... osomal rearrangements in mice.
@en
P2093
P2860
P304
P356
10.1093/NAR/27.11.2354
P407
P577
1999-06-01T00:00:00Z