Analysis of Fgf8 gene function in vertebrate development.
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Mice deficient in the fused homolog do not exhibit phenotypes indicative of perturbed hedgehog signaling during embryonic developmentDmrt1, a gene related to worm and fly sexual regulators, is required for mammalian testis differentiationTargeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clustersGABAA receptor gamma 2 subunit knockdown mice have enhanced anxiety-like behavior but unaltered hypnotic response to benzodiazepines.Androgen receptor (AR) pathophysiological roles in androgen-related diseases in skin, bone/muscle, metabolic syndrome and neuron/immune systems: lessons learned from mice lacking AR in specific cellsLoss of the Greatwall Kinase Weakens the Spindle Assembly CheckpointCharacterization of the Gbx1-/- mouse mutant: a requirement for Gbx1 in normal locomotion and sensorimotor circuit developmentAbnormal sperm in mice lacking the Taf7l genePolycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosisMeiotic failure in male mice lacking an X-linked factorPalmitoylation is required for the production of a soluble multimeric Hedgehog protein complex and long-range signaling in vertebratesOverlapping role of dynamin isoforms in synaptic vesicle endocytosisKidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneysA genetic assay for transcription errors reveals multilayer control of RNA polymerase II fidelityOTX2 Transcription Factor Controls Regional Patterning within the Medial Ganglionic Eminence and Regional Identity of the SeptumCorrect patterning of the primitive streak requires the anterior visceral endodermMice mutant in the DM domain gene Dmrt4 are viable and fertile but have polyovular folliclesMouse MOV10L1 associates with Piwi proteins and is an essential component of the Piwi-interacting RNA (piRNA) pathwayThe folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell developmentRAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in femalesThe ECM protein nephronectin promotes kidney development via integrin alpha8beta1-mediated stimulation of Gdnf expressionThe Shh-independent activator function of the full-length Gli3 protein and its role in vertebrate limb digit patterningA differential developmental pattern of spinal interneuron apoptosis during synaptogenesis: insights from genetic analyses of the protocadherin-gamma gene clusterVascular development of the brain requires beta8 integrin expression in the neuroepitheliumBMP4 is required in the anterior heart field and its derivatives for endocardial cushion remodeling, outflow tract septation, and semilunar valve developmentgamma-Protocadherins regulate neuronal survival but are dispensable for circuit formation in retinaNeural crest requires Impdh2 for development of the enteric nervous system, great vessels, and craniofacial skeletonTargeted Deletion of Kynurenine 3-Monooxygenase in Mice: A NEW TOOL FOR STUDYING KYNURENINE PATHWAY METABOLISM IN PERIPHERY AND BRAINEfficient mapping of transgene integration sites and local structural changes in Cre transgenic mice using targeted locus amplification.Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.Bone marrow-derived cells contribute to epithelial engraftment during wound healingSprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryoConstitutive reductions in mTOR alter cell size, immune cell development, and antibody production.Non-canonical wnt signals antagonize and canonical wnt signals promote cell proliferation in early kidney development.NeuroD1 is required for survival of photoreceptors but not pinealocytes: results from targeted gene deletion studies.Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome.CRISPR-Cas9 knockin mice for genome editing and cancer modelingCooperative and independent functions of FGF and Wnt signaling during early inner ear development.Esrrb-Cre excises loxP-flanked alleles in early four-cell embryos.Genetic mosaic analysis based on Cre recombinase and navigated laser capture microdissection.
P2860
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P2860
Analysis of Fgf8 gene function in vertebrate development.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Analysis of Fgf8 gene function in vertebrate development.
@en
Analysis of Fgf8 gene function in vertebrate development.
@nl
type
label
Analysis of Fgf8 gene function in vertebrate development.
@en
Analysis of Fgf8 gene function in vertebrate development.
@nl
prefLabel
Analysis of Fgf8 gene function in vertebrate development.
@en
Analysis of Fgf8 gene function in vertebrate development.
@nl
P2093
P1476
Analysis of Fgf8 gene function in vertebrate development.
@en
P2093
Lewandoski M
P304
P577
1997-01-01T00:00:00Z