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| - vědecký článek publikovaný v roce 1995 (cs)
- artículu científicu espublizáu en 1995 (ast)
- 1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված (hy)
- наукова стаття, опублікована у вересні 1995 (uk)
- 1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած (hyw)
- article scientifique publié en 1995 (fr)
- scientific journal article (en)
- im September 1995 veröffentlichter wissenschaftlicher Artikel (de)
- wetenschappelijk artikel (gepubliceerd op 1995/09/20) (nl)
- vedecký článok (publikovaný 1995/09/20) (sk)
- مقالة علمية (نشرت في 20-9-1995) (ar)
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| author name string
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| author name string
| - K. R. Johnson
- P. W. Lane
- M. T. Davisson
- P. Ward-Bailey
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| rdfs:label
| - Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (en)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (nl)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (ast)
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| skos:prefLabel
| - Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (en)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (nl)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (ast)
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| name
| - Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (en)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (nl)
- Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (ast)
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| title
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| title
| - Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac (en)
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| - release_zp3ot54rhva4pdrmsow2mrhtqe
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| is about
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| is cites work
of | - Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3.
- Split hand foot malformation is associated with a reduced level of Dactylin gene expression
- The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development
- Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome
- A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant
- Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome
- A symphony of regulations centered on p63 to control development of ectoderm-derived structures
- Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3.
- Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update.
- A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24
- Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25
- Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.
- Proviral insertions in the zebrafish hagoromo gene, encoding an F-box/WD40-repeat protein, cause stripe pattern anomalies.
- Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype
- Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity
- Modifier genes and the plasticity of genetic networks in mice
- Pathogenesis of ectrodactyly in the Dactylaplasia mouse: aberrant cell death of the apical ectodermal ridge
- Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation
- The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene
- Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.
- Split-hand/foot malformation - molecular cause and implications in genetic counseling.
- Taking stock of complex trait genetics in mice
- Genetic analysis of Gv1, a gene controlling transcription of endogenous murine polytropic proviruses
- Mechanism of homophilic binding mediated by ninjurin, a novel widely expressed adhesion molecule
- Patterson-Stevenson-Fontaine syndrome: 30-year follow-up and clinical details of a further affected case
- Wolf-Hirschhorn syndrome and a split-hand malformation
- Mouse germ line mutations due to retrotransposon insertions
- Discovery Genetics - The History and Future of Spontaneous Mutation Research
- Backfoot, a novel homeobox gene, maps to human chromosome 5 (BFT) and mouse chromosome 13 (Bft)
- Distal limb malformations: underlying mechanisms and clinical associations
- Copy-number variants and candidate gene mutations in isolated split hand/foot malformation.
- A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice
- Rare missense variant p.Ala505Ser in the ZAK protein observed in a patient with split-hand/foot malformation from a non-consanguineous pedigree
- Duplication of 10q24 locus: broadening the clinical and radiological spectrum
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