(Q52192748)

26 April 2018

title

Point mutations in human GLI3 cause Greig syndrome. (English)

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26 April 2018

author name string

Wild A

1

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26 April 2018

Kalff-Suske M

2

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26 April 2018

Vortkamp A

3

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26 April 2018

Bornholdt D

4

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26 April 2018

König R

5

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26 April 2018

Grzeschik KH

6

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26 April 2018

publication date

1 October 1997

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26 April 2018

published in

Human Molecular Genetics

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26 April 2018

volume

6

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26 April 2018

page(s)

1979-1984

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issue

11

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Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

The GLI-Kruppel family of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Serpentine proteins slither into the wingless and hedgehog fields

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

The Drosophila smoothened gene encodes a seven-pass membrane protein, a putative receptor for the hedgehog signal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Conservation of the hedgehog/patched signaling pathway from flies to mice: induction of a mouse patched gene by Hedgehog

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Drosophila CBP is a co-activator of cubitus interruptus in hedgehog signalling.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

Isolation and characterization of a cosmid contig for the GCPS gene region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1979

21 January 2018

Identifiers

DOI

10.1093/HMG/6.11.1979

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26 April 2018

PubMed ID

9302279

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26 April 2018