X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation.
about
Molecular basis of cleft palates in miceGlycosyl phosphatidylinositol anchor biosynthesis is essential for maintaining epithelial integrity during Caenorhabditis elegans embryogenesisGPI-anchor synthesis is indispensable for the germline development of the nematode Caenorhabditis elegans.Phenotypic and functional characterization of a mouse model of targeted Pig-a deletion in hematopoietic cellsCre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target gene.Genetic and therapeutic targeting of properdin in mice prevents complement-mediated tissue injury.Cre-mediated germline mosaicism: a new transgenic mouse for the selective removal of residual markers from tri-lox conditional alleles.Simultaneous measurement of benzo[a]pyrene-induced Pig-a and lacZ mutations, micronuclei and DNA adducts in Muta™ Mouse.The phenotype of a germline mutation in PIGA: the gene somatically mutated in paroxysmal nocturnal hemoglobinuria.pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability.FES-Cre targets phosphatidylinositol glycan class A (PIGA) inactivation to hematopoietic stem cells in the bone marrowErythrocyte-based Pig-a gene mutation assay: demonstration of cross-species potential.Mutation analysis with random DNA identifiers (MARDI) catalogs Pig-a mutations in heterogeneous pools of CD48-deficient T cells derived from DMBA-treated rats.Early frameshift mutation in PIGA identified in a large XLID family without neonatal lethality.Tissue-inherent fate of GPI revealed by GPI-anchored GFP transgenesis.Convergent extension movements in growth plate chondrocytes require gpi-anchored cell surface proteins.Evaluation of in vivo genotoxicity induced by N-ethyl-N-nitrosourea, benzo[a]pyrene, and 4-nitroquinoline-1-oxide in the Pig-a and gpt assays.A recurrent germline mutation in the PIGA gene causes Simpson-Golabi-Behmel syndrome type 2.Chimaeric mice with disruption of the gene coding for phosphatidylinositol glycan class A (Pig-a) were defective in embryogenesis and spermatogenesis.Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice.A novel germline PIGA mutation in Ferro-Cerebro-Cutaneous syndrome: a neurodegenerative X-linked epileptic encephalopathy with systemic iron-overload.
P2860
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P2860
X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@ast
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@en
type
label
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@ast
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@en
prefLabel
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@ast
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@en
P2093
P2860
P356
P1476
X inactivation and somatic cel ...... carrying a Piga-null mutation.
@en
P2093
P2860
P304
P356
10.1073/PNAS.96.13.7479
P407
P577
1999-06-01T00:00:00Z