(Q72090638)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference

1

1 reference

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23 October 2019

author name string

S I Oda

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

U Rüther

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

publication date

1 June 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

number of pages

3

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

volume

5

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23 October 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

page(s)

384-386

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00356560

23 October 2019

exact match

0 references

1 reference

12 December 2020

GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity

1 reference

12 December 2020

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

1 reference

12 December 2020

Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes)

1 reference

12 December 2020

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

1 reference

12 December 2020

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)

1 reference

12 December 2020

A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene

1 reference

12 December 2020

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt)

1 reference

12 December 2020

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)

1 reference

12 December 2020

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

12 December 2020

Mouse small eye results from mutations in a paired-like homeobox-containing gene

1 reference

12 December 2020

Molecular analysis of the C. elegans sex-determining gene tra-1: a gene encoding two zinc finger proteins

1 reference

12 December 2020

Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt)

1 reference

12 December 2020

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

1 reference

12 December 2020

Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.

1 reference

12 December 2020

Polydactyly Nagoya, Pdn: A new mutant gene in the mouse

1 reference

12 December 2020

Molecular linkage of the morphogenetic mutation add and the zinc finger gene Gli3

1 reference

12 December 2020

Developmental brain abnormalities accompanied with the retarded production of S-100 beta protein in genetic polydactyly mice.

1 reference

12 December 2020

Occurrences and linkage relations of the mutant ‘extra-toes’ in the mouse

1 reference

12 December 2020

Localization of genes and anonymous DNA probes on the short arm of Chromosome 7

1 reference

12 December 2020

Zinc finger point mutations within the WT1 gene in Wilms tumor patients

1 reference

12 December 2020

The molecular basis of the undulated/Pax-1 mutation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00356560

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8043956%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference