(Q34390140)

English

The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

based on heuristic

inferred from title

postaxial polydactyly

1 reference

based on heuristic

inferred from title

Stilianos Antonarakis

12

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Radhakrishna U

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

Bornholdt D

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Scott HS

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Patel UC

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Rossier C

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Engel H

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Bottani A

7

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Chandal D

8

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Blouin JL

9

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Solanki JV

10

1 reference

Europe PubMed Central

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1 August 2017

Grzeschik KH

11

1 reference

Europe PubMed Central

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1 August 2017

language of work or name

0 references

publication date

1 September 1999

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Europe PubMed Central

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1 August 2017

American Journal of Human Genetics

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Europe PubMed Central

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1 August 2017

65

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Europe PubMed Central

PubMed publication ID

1 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

645-655

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

GLI3 mutations in human disorders mimic Drosophila cubitus interruptus protein functions and localization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Gene structure and allelic expression assay of the human GLI3 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Mutation in GLI3 in postaxial polydactyly type A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Strike three for GLI3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Costal2, a Novel Kinesin-Related Protein in the Hedgehog Signaling Pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Hedgehog Elicits Signal Transduction by Means of a Large Complex Containing the Kinesin-Related Protein Costal2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Catching a Gli-mpse of Hedgehog

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Proteolysis That Is Inhibited by Hedgehog Targets Cubitus interruptus Protein to the Nucleus and Converts It to a Repressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Sending and receiving the hedgehog signal: control by the Drosophila Gli protein Cubitus interruptus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Faster sequential genetic linkage computations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

The new dysmorphology: application of insights from basic developmental biology to the understanding of human birth defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

Cloning and characterization of the segment polarity gene cubitus interruptus Dominant of Drosophila

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

28 July 2018

The mouse mutation Pdn (Polydactyly Nagoya) is caused by the integration of a retrotransposon into the Gli3 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

27 October 2018

Point Mutations in Human GLI3 Cause Greig Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

27 October 2018

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

27 October 2018

Greig cephalopolysyndactyly: report of 13 affected individuals in three families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377970

27 October 2018

Crossed polydactyly type I in a mother and son: an autosomal dominant trait?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Indian family with postaxial polydactyly in four generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preaxial polydactyly type 4: variability in a large kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441570

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

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