NEW SPLOTCH ALLELES IN THE MOUSE

scientific article published on 01 May 1964

NEW SPLOTCH ALLELES IN THE MOUSE is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/OXFORDJOURNALS.JHERED.A107317
P953full work available at URLhttp://academic.oup.com/jhered/article-pdf/55/3/97/2344661/55-3-97.pdf
P698PubMed publication ID14170406

P2093author name stringM. M. DICKIE
P407language of work or nameEnglishQ1860
P921main subjectgeneticsQ7162
biotechnologyQ7108
alleleQ80726
P304page(s)97-101
P577publication date1964-05-01
P1433published inJournal of HeredityQ6295280
P1476titleNEW SPLOTCH ALLELES IN THE MOUSE
P478volume55

Reverse relations

cites work (P2860)
Q36059319A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant
Q48603039Altered cell proliferation in the spinal cord of mouse neural tube mutants curly tail and Pax3 splotch-delayed
Q24608570Bone ridge patterning during musculoskeletal assembly is mediated through SCX regulation of Bmp4 at the tendon-skeleton junction
Q45714500Effects of folate supplementation on the risk of spontaneous and induced neural tube defects in Splotch mice
Q42722333Functional interaction between Foxd3 and Pax3 in cardiac neural crest development
Q41633803Genetic landmarks for defects in mouse neural tube closure
Q36153596Human neural tube defects: developmental biology, epidemiology, and genetics
Q30877319Methodology for the inference of gene function from phenotype data
Q44036292Mouse chromosome 1.
Q47073931Muscle contraction controls skeletal morphogenesis through regulation of chondrocyte convergent extension
Q52189581Neurulation abnormalities secondary to altered gene expression in neural tube defect susceptible Splotch embryos.
Q53987464Patterns of neuronal differentiation in neural tube mutant mice: curly tail and Pax3 splotch-delayed.
Q28265323Persistent truncus arteriosus in the Splotch mutant mouse
Q37317139Pigmentation PAX-ways: the role of Pax3 in melanogenesis, melanocyte stem cell maintenance, and disease
Q72264586Sex differences in recombination of linked genes in animals
Q24514967Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans
Q70763083The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature
Q36716847The developmental biology of melanocytes and its application to understanding human congenital disorders of pigmentation
Q32079186Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf.
Q36422278Transcriptional analyses of two mouse models of spina bifida
Q28585890splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

Search more.