scholarly article | Q13442814 |
P356 | DOI | 10.1093/OXFORDJOURNALS.JHERED.A107317 |
P953 | full work available at URL | http://academic.oup.com/jhered/article-pdf/55/3/97/2344661/55-3-97.pdf |
P698 | PubMed publication ID | 14170406 |
P2093 | author name string | M. M. DICKIE | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | genetics | Q7162 |
biotechnology | Q7108 | ||
allele | Q80726 | ||
P304 | page(s) | 97-101 | |
P577 | publication date | 1964-05-01 | |
P1433 | published in | Journal of Heredity | Q6295280 |
P1476 | title | NEW SPLOTCH ALLELES IN THE MOUSE | |
P478 | volume | 55 |
Q36059319 | A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant |
Q48603039 | Altered cell proliferation in the spinal cord of mouse neural tube mutants curly tail and Pax3 splotch-delayed |
Q24608570 | Bone ridge patterning during musculoskeletal assembly is mediated through SCX regulation of Bmp4 at the tendon-skeleton junction |
Q45714500 | Effects of folate supplementation on the risk of spontaneous and induced neural tube defects in Splotch mice |
Q42722333 | Functional interaction between Foxd3 and Pax3 in cardiac neural crest development |
Q41633803 | Genetic landmarks for defects in mouse neural tube closure |
Q36153596 | Human neural tube defects: developmental biology, epidemiology, and genetics |
Q30877319 | Methodology for the inference of gene function from phenotype data |
Q44036292 | Mouse chromosome 1. |
Q47073931 | Muscle contraction controls skeletal morphogenesis through regulation of chondrocyte convergent extension |
Q52189581 | Neurulation abnormalities secondary to altered gene expression in neural tube defect susceptible Splotch embryos. |
Q53987464 | Patterns of neuronal differentiation in neural tube mutant mice: curly tail and Pax3 splotch-delayed. |
Q28265323 | Persistent truncus arteriosus in the Splotch mutant mouse |
Q37317139 | Pigmentation PAX-ways: the role of Pax3 in melanogenesis, melanocyte stem cell maintenance, and disease |
Q72264586 | Sex differences in recombination of linked genes in animals |
Q24514967 | Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans |
Q70763083 | The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature |
Q36716847 | The developmental biology of melanocytes and its application to understanding human congenital disorders of pigmentation |
Q32079186 | Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf. |
Q36422278 | Transcriptional analyses of two mouse models of spina bifida |
Q28585890 | splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3 |
Search more.