Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
about
P1343
The Opitz syndrome gene product, MID1, associates with microtubulesCloning and characterization of a novel RING finger protein that interacts with class V myosinsTRIM40 promotes neddylation of IKKγ and is downregulated in gastrointestinal cancersPhosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4.New insights into craniofacial malformationsThe Ret finger protein induces apoptosis via its RING finger-B box-coiled-coil motifVestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidaseAn Oak Ridge legacy: the specific locus test and its role in mouse mutagenesisCloning and characterization of a novel RING-B-box-coiled-coil protein with apoptotic functionRegulation of microtubule dynamics and myogenic differentiation by MURF, a striated muscle RING-finger proteinMouse mutants from chemically mutagenized embryonic stem cellsGeneration of induced pluripotent stem cells from the prairie voleUnraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Hedgehog-dependent E3-ligase Midline1 regulates ubiquitin-mediated proteasomal degradation of Pax6 during visual system development.The E3 ubiquitin ligase- and protein phosphatase 2A (PP2A)-binding domains of the Alpha4 protein are both required for Alpha4 to inhibit PP2A degradation.Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutationsMonoubiquitination promotes calpain cleavage of the protein phosphatase 2A (PP2A) regulatory subunit α4, altering PP2A stability and microtubule-associated protein phosphorylation.A novel Netrin-1-sensitive mechanism promotes local SNARE-mediated exocytosis during axon branching.Enterophilins, a new family of leucine zipper proteins bearing a b30.2 domain and associated with enterocyte differentiation.A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice.Underdeveloped uterus and reduced estrogen responsiveness in mice with disruption of the estrogen-responsive finger protein gene, which is a direct target of estrogen receptor alpha.GNIP, a novel protein that binds and activates glycogenin, the self-glucosylating initiator of glycogen biosynthesis.Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organizationChromosomal transposition of a Tc1/mariner-like element in mouse embryonic stem cellsDevelopment of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in miceDouble trans-chromosomic mice: maintenance of two individual human chromosome fragments containing Ig heavy and kappa loci and expression of fully human antibodiesFunctional 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.Modifier screens in the mouse: time to move forward with reverse genetics.Production of alpha-1,3-galactosyltransferase null pigs by means of nuclear transfer with fibroblasts bearing loss of heterozygosity mutations.Mutations in Serac1 or Synj2 cause proximal t haplotype-mediated male mouse sterility but not transmission ratio distortion.Efficient chromosomal transposition of a Tc1/mariner- like transposon Sleeping Beauty in mice.N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express.A chromosomal deletion map of human malformations.Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian biology.A mouse geneticist's practical guide to CRISPR applications.Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding.Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths.Embryonic lethality and tumorigenesis caused by segmental aneuploidy on mouse chromosome 11.N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.Physical mapping of male fertility and meiotic drive quantitative trait loci in the mouse t complex using chromosome deficiencies
P2860
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P2860
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@en
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@nl
type
label
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@en
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@nl
prefLabel
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@en
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@nl
P2093
P2860
P356
P1433
P1476
Chromosomal deletion complexes in mice by radiation of embryonic stem cells.
@en
P2093
Bergstrom R
Jaenisch R
Lederman B
Schimenti J
P2860
P2888
P304
P356
10.1038/NG0397-285
P407
P4510
P577
1997-03-01T00:00:00Z
P6179
1004743246