(Q60955575)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

15

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7 January 2020

author name string

Michelle Segalov

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

William Sewell

10

1 reference

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7 January 2020

Hyun-Duck Nah

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Kenro Kusumi

16

1 reference

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7 January 2020

Kathleen M Loomes

1

1 reference

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7 January 2020

Stacey A Stevens

2

1 reference

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7 January 2020

Megan L O'Brien

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Dorian M Gonzalez

4

1 reference

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7 January 2020

Matthew J Ryan

5

1 reference

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7 January 2020

Nicholas J Dormans

7

1 reference

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7 January 2020

Mizuho S Mimoto

8

1 reference

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7 January 2020

Joshua D Gibson

9

1 reference

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7 January 2020

Alyssa A Schaffer

11

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7 January 2020

Eric F Rappaport

13

1 reference

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7 January 2020

Stephen C Pratt

14

1 reference

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7 January 2020

publication date

1 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

published in

Developmental Dynamics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

236

1 reference

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7 January 2020

issue

10

1 reference

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7 January 2020

page(s)

2943-2951

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

Expression of chick Barx-1 and its differential regulation by FGF-8 and BMP signaling in the maxillary primordia.

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Id4 is required for the correct timing of neural differentiation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Jag2-Notch1 signaling regulates oral epithelial differentiation and palate development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Mice lacking both presenilin genes exhibit early embryonic patterning defects

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

The Notch target genes Hey1 and Hey2 are required for embryonic vascular development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Mutations in NOTCH1 cause aortic valve disease

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

The long and short of it: somite formation in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

HES and HERP families: multiple effectors of the Notch signaling pathway

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Id4 expression and its relationship to other Id genes during avian embryonic development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Notch signaling regulates left-right asymmetry determination by inducing Nodal expression

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Maturity assessment and curve progression in girls with idiopathic scoliosis.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

The divergent DSL ligand Dll3 does not activate Notch signaling but cell autonomously attenuates signaling induced by other DSL ligands

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Inhibition of Jagged-mediated Notch signaling disrupts zebrafish biliary development and generates multi-organ defects compatible with an Alagille syndrome phenocopy

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Molecular analysis of congenital scoliosis: a candidate gene approach

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Expression profiling of transforming growth factor beta superfamily genes in developing orofacial tissue

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Expression analysis of a Notch homologue in the mouse embryo.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Specification and segmentation of the paraxial mesoderm.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Barx1, a new mouse homeodomain transcription factor expressed in cranio-facial ectomesenchyme and the stomach

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Transformation of tooth type induced by inhibition of BMP signaling

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Abnormal vertebral segmentation and the notch signaling pathway in man.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Id4 regulates neural progenitor proliferation and differentiation in vivo

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

A mutation in the Lunatic fringe gene suppresses the effects of a Jagged2 mutation on inner hair cell development in the cochlea

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21296

7 January 2021

Identifiers

DOI

10.1002/DVDY.21296

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17849441%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference