(Q28145579)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10835638%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination (English)

1 reference

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7 November 2019

1 reference

1

1 reference

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7 November 2019

David Wotton

2

1 reference

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7 November 2019

Joan Massagué Solé

9

1 reference

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7 November 2019

author name string

M C Edwards

3

1 reference

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7 November 2019

E Roessler

4

1 reference

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7 November 2019

L Ades

5

1 reference

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7 November 2019

P Meinecke

6

1 reference

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7 November 2019

A Richieri-Costa

7

1 reference

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7 November 2019

E H Zackai

8

1 reference

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7 November 2019

M Muenke

10

1 reference

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7 November 2019

S J Elledge

11

1 reference

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7 November 2019

language of work or name

English

0 references

publication date

1 June 2000

1 reference

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7 November 2019

1 reference

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7 November 2019

volume

25

1 reference

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7 November 2019

page(s)

205-208

1 reference

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7 November 2019

issue

2

1 reference

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Holoprosencephaly: a defect in brain patterning.

7 November 2019

cites work

1 reference

7 January 2021

Holoprosencephaly: from Homer to Hedgehog.

1 reference

7 January 2021

Holoprosencephaly in infants of diabetic mothers

1 reference

7 January 2021

Holoprosencephaly: a paradigm for the complex genetics of brain development.

1 reference

7 January 2021

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

1 reference

7 January 2021

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

1 reference

7 January 2021

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

1 reference

7 January 2021

Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling.

1 reference

7 January 2021

cyclops encodes a nodal-related factor involved in midline signaling

1 reference

7 January 2021

Zebrafish organizer development and germ-layer formation require nodal-related signals.

1 reference

7 January 2021

The EGF-CFC protein one-eyed pinhead is essential for nodal signaling

1 reference

7 January 2021

Smad2 role in mesoderm formation, left-right patterning and craniofacial development

1 reference

7 January 2021

A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif

1 reference

7 January 2021

A Smad transcriptional corepressor

1 reference

7 January 2021

TGF-beta signal transduction

1 reference

7 January 2021

The Ski oncoprotein interacts with the Smad proteins to repress TGFbeta signaling

1 reference

7 January 2021

Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation.

1 reference

7 January 2021

Multiple modes of repression by the Smad transcriptional corepressor TGIF

1 reference

7 January 2021

Carboxy-terminally truncated Gli3 proteins associate with Smads

1 reference

7 January 2021

Left-right asymmetry in vertebrates

1 reference

7 January 2021

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

1 reference

7 January 2021

Identifiers

DOI

10.1038/76074

2 references

Consolidated OpenCitations Corpus – April 2017

21678

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10835638%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

21678

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

21678

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10835638%20AND%20SRC:MED&resulttype=core&format=json