(Q24306605)

specification of axis polarity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

9

Leslie G Biesecker

Leslie G

Biesecker

1 reference

9 December 2023

8

Ann Nordgren

Ann

Nordgren

1 reference

9 December 2023

Emma N Hilton

1

Emma N

Hilton

1 reference

9 December 2023

Forbes D C Manson

2

Forbes D C

Manson

1 reference

9 December 2023

Jill E Urquhart

3

Jill E

Urquhart

1 reference

9 December 2023

Jennifer J Johnston

4

Jennifer J

Johnston

1 reference

9 December 2023

Anne M Slavotinek

5

Anne M

Slavotinek

1 reference

9 December 2023

Peter Hedera

6

Peter

Hedera

1 reference

9 December 2023

Eva-Lena Stattin

7

Eva-Lena

Stattin

1 reference

9 December 2023

Graeme C M Black

10

Graeme C M

Oculo‐facio‐cardio‐dental syndrome: Skewed X chromosome inactivation in mother and daughter suggest X‐linked dominant Inheritance

Black

1 reference

9 December 2023

language of work or name

English

0 references

publication date

15 July 2007

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published in

Human Molecular Genetics

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volume

16

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issue

14

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page(s)

1773-82

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cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Pilot morpholino screen in Xenopus tropicalis identifies a novel gene involved in head development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Cardiac patterning and morphogenesis in zebrafish

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Confocal imaging of early heart development in Xenopus laevis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Regulation of gut and heart left-right asymmetry by context-dependent interactions between xenopus lefty and BMP4 signaling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. .

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Rieger syndrome: a clinical, molecular, and biochemical analysis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Insights into the genetic basis of congenital heart disease.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Asplenia syndrome: insight into embryology through an analysis of cardiac and extracardiac anomalies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

X-linked situs abnormalities result from mutations in ZIC3

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Left-right asymmetry in the vertebrate embryo: from early information to higher-level integration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

The mixed lineage leukemia fusion partner AF9 binds specific isoforms of the BCL-6 corepressor

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Heterotaxy: associated conditions and hospital-based prevalence in newborns

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Heterotaxia syndromes and their abdominal manifestations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Control of inflammation, cytokine expression, and germinal center formation by BCL-6

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Polycomb group and SCF ubiquitin ligases are found in a novel BCOR complex that is recruited to BCL6 targets

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Heterotaxy syndrome -- asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021

Left-right lineage analysis of the embryonic Xenopus heart reveals a novel framework linking congenital cardiac defects and laterality disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM125

7 January 2021