Genetic dissection ofPitx2in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration (Q44659652)

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scientific article published on December 1, 2003

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English	Genetic dissection ofPitx2in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration	scientific article published on December 1, 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Genetic dissection ofPitx2in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration (English)

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

author name string

Wei Liu

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Jennifer Selever

2

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Mei-Fang Lu

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

James F. Martin

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14623826

3 April 2024

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publication date

1 December 2003

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Europe PubMed Central

PubMed publication ID

5 December 2017

number of pages

11

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full work available at URL

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Europe PubMed Central

PubMed publication ID

5 December 2017

130

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Europe PubMed Central

PubMed publication ID

5 December 2017

25

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Europe PubMed Central

PubMed publication ID

5 December 2017

6375-6385

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Europe PubMed Central

PubMed publication ID

5 December 2017

Axenfeld-Rieger syndrome in the age of molecular genetics

1

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

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

2

1 reference

10.1242/DEV.00849

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3 April 2024

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

4

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Mechanisms of left-right determination in vertebrates

5

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Differential regulation of gene expression by PITX2 isoforms

6

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Reprogrammable recognition codes in bicoid homeodomain-DNA interaction

7

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny

8

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Gradient formation of the TGF-beta homolog Dpp.

9

1 reference

10.1242/DEV.00849

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3 April 2024

Widespread recombinase expression using FLPeR (flipper) mice

11

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

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

12

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene

13

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Coactivation of Rac and Rho by Wnt/Frizzled signaling is required for vertebrate gastrulation

15

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Links in the left/right axial pathway.

16

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during development

17

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.

19

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

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

20

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

23

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

FGF signaling is necessary for the specification of the odontogenic mesenchyme.

24

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Pitx1 and Pitx2 are required for development of hindlimb buds.

25

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Expression of the transcription factors Otlx2, Barx1 and Sox9 during mouse odontogenesis.

26

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation

27

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning

28

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

29

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome

30

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Identification of a dominant negative homeodomain mutation in Rieger syndrome

31

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Dominant negative dimerization of a mutant homeodomain protein in Axenfeld-Rieger syndrome

32

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Pitx2 isoforms: involvement of Pitx2c but not Pitx2a or Pitx2b in vertebrate left-right asymmetry

33

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

34

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Ectodermally derived FGF8 defines the maxillomandibular region in the early chick embryo: epithelial-mesenchymal interactions in the specification of the craniofacial ectomesenchyme

35

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Two-step regulation of left-right asymmetric expression of Pitx2: initiation by nodal signaling and maintenance by Nkx2.

36

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Analysis of three Ptx2 splice variants on transcriptional activity and differential expression pattern in the brain

37

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage.

38

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

The role of RhoA in tissue polarity and Frizzled signalling

39

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Dpp gradient formation in the Drosophila wing imaginal disc

41

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch

43

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Transformation of tooth type induced by inhibition of BMP signaling

44

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development

46

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Pitx2a expression alters actin-myosin cytoskeleton and migration of HeLa cells through Rho GTPase signaling

47

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Cooperative dimerization of paired class homeo domains on DNA.

48

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse

49

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Drosophila Rho-associated kinase (Drok) links Frizzled-mediated planar cell polarity signaling to the actin cytoskeleton.

50

1 reference

10.1242/DEV.00849

https://api.crossref.org/works/10.1242/DEV.00849

3 April 2024

Identifiers

10.1242/DEV.00849

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

ResearchGate publication ID

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