scholarly article | Q13442814 |
P356 | DOI | 10.1002/GENE.20071 |
P698 | PubMed publication ID | 15384171 |
P50 | author | Jonathan Flint | Q37374224 |
Jennifer Davies | Q43086195 | ||
Roger Cox | Q60699053 | ||
Michelle Goldsworthy | Q61798145 | ||
Nick Warr | Q64362248 | ||
David Keays | Q66678462 | ||
P2093 | author name string | Valerie Wilson | |
Debora Bogani | |||
Pat Nolan | |||
Ruth Arkell | |||
Paul Elms | |||
Zuzanna Tymowska-Lalanne | |||
P2860 | cites work | Cloning of the T gene required in mesoderm formation in the mouse | Q28236865 |
Crooked tail (Cd) models human folate-responsive neural tube defects | Q28508865 | ||
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 locus | Q28512134 | ||
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3 | Q28585890 | ||
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse | Q28592309 | ||
MGD: the Mouse Genome Database | Q39790334 | ||
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus | Q42631687 | ||
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 mouse | Q72767865 | ||
A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects | Q73911021 | ||
P433 | issue | 2 | |
P921 | main subject | Brachyury, T-box transcription factor T | Q14885923 |
Paired box 3 | Q14916252 | ||
Low density lipoprotein receptor-related protein 6 | Q21495922 | ||
Zinc finger protein ZIC 2 | Q21984265 | ||
Ribosomal protein S7 | Q21989103 | ||
Zinc finger protein of the cerebellum 3 | Q21992049 | ||
P304 | page(s) | 109–117 | |
P577 | publication date | 2004-10-01 | |
P1433 | published in | Genesis | Q5532784 |
P1476 | title | New semidominant mutations that affect mouse development | |
P478 | volume | 40 |
Q35755034 | A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice |
Q24631597 | A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation |
Q41244959 | A new missense mutation in the paired domain of the mouse Pax3 gene |
Q28513404 | Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen |
Q28509829 | Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease |
Q42920653 | Identification of a Novel Mouse Brachyury (T) Allele Causing a Short Tail Mutation in Mice |
Q37383064 | Modeling neural tube defects in the mouse |
Q27329518 | Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes |
Q33584524 | Networks and pathways in pigmentation, health, and disease |
Q21559671 | Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes |
Q48081611 | Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse. |
Q36487730 | The role of mutagenesis in defining genes in behaviour |
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