New semidominant mutations that affect mouse development

scientific journal article

New semidominant mutations that affect mouse development is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/GENE.20071
P698PubMed publication ID15384171

P50authorJonathan FlintQ37374224
Jennifer DaviesQ43086195
Roger CoxQ60699053
Michelle GoldsworthyQ61798145
Nick WarrQ64362248
David KeaysQ66678462
P2093author name stringValerie Wilson
Debora Bogani
Pat Nolan
Ruth Arkell
Paul Elms
Zuzanna Tymowska-Lalanne
P2860cites workCloning of the T gene required in mesoderm formation in the mouseQ28236865
Crooked tail (Cd) models human folate-responsive neural tube defectsQ28508865
The hematopoietic growth factor KL is encoded by the Sl locus and is the ligand of the c-kit receptor, the gene product of the W locusQ28512134
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3Q28585890
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouseQ28592309
MGD: the Mouse Genome DatabaseQ39790334
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locusQ42631687
Genome-wide, large-scale production of mutant mice by ENU mutagenesis.Q43520565
Zic2 is required for neural crest formation and hindbrain patterning during mouse development.Q48128104
Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development.Q52202953
The T genes in embryogenesis.Q52215459
Efficient localization of mutations by interval haplotype analysis.Q52249652
Curtailed, a new dominant T-allele in the house mouseQ72767865
A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defectsQ73911021
P433issue2
P921main subjectBrachyury, T-box transcription factor TQ14885923
Paired box 3Q14916252
Low density lipoprotein receptor-related protein 6Q21495922
Zinc finger protein ZIC 2Q21984265
Ribosomal protein S7Q21989103
Zinc finger protein of the cerebellum 3Q21992049
P304page(s)109–117
P577publication date2004-10-01
P1433published inGenesisQ5532784
P1476titleNew semidominant mutations that affect mouse development
P478volume40

Reverse relations

cites work (P2860)
Q35755034A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice
Q24631597A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation
Q41244959A new missense mutation in the paired domain of the mouse Pax3 gene
Q28513404Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
Q28509829Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease
Q42920653Identification of a Novel Mouse Brachyury (T) Allele Causing a Short Tail Mutation in Mice
Q37383064Modeling neural tube defects in the mouse
Q27329518Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes
Q33584524Networks and pathways in pigmentation, health, and disease
Q21559671Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes
Q48081611Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse.
Q36487730The role of mutagenesis in defining genes in behaviour

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