PITX2 gain-of-function in Rieger syndrome eye model. (Q35103384)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15509533%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

PITX2 gain-of-function in Rieger syndrome eye model (English)

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4 January 2020

2

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4 January 2020

author name string

Johan Holmberg

series ordinal

1

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4 January 2020

Tord A Hjalt

series ordinal

3

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4 January 2020

language of work or name

English

0 references

publication date

1 November 2004

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The American Journal of Pathology

4 January 2020

published in

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4 January 2020

volume

165

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4 January 2020

issue

5

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4 January 2020

page(s)

1633-1641

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The Wnt/beta-catenin-->Pitx2 pathway controls the turnover of Pitx2 and other unstable mRNAs

4 January 2020

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

9 July 2018

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9 July 2018

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

9 July 2018

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9 July 2018

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

9 July 2018

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Identification of a dominant negative homeodomain mutation in Rieger syndrome

9 July 2018

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PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndrome

9 July 2018

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9 July 2018

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Identification of a 3.2 kb 5'-flanking region of the murine keratocan gene that directs beta-galactosidase expression in the adult corneal stroma of transgenic mice

9 July 2018

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The Pitx2 protein in mouse development

9 July 2018

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The mutated human gene encoding hepatocyte nuclear factor 1beta inhibits kidney formation in developing Xenopus embryos

9 July 2018

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Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta

9 July 2018

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Molecular basis of left-right asymmetry

9 July 2018

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

9 July 2018

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

9 July 2018

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Dosage requirement of Pitx2 for development of multiple organs

9 July 2018

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The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping

9 July 2018

1 reference

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The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities

9 July 2018

1 reference

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Collagen hydroxylases and the protein disulfide isomerase subunit of prolyl 4-hydroxylases

9 July 2018

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The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

9 July 2018

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

9 July 2018

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Number of people with glaucoma worldwide

9 July 2018

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

9 July 2018

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Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

9 July 2018

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Immunobiochemical and molecular biologic characterization of the cell proliferation-associated nuclear antigen that is defined by monoclonal antibody Ki-67

9 July 2018

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9 July 2018

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9 July 2018

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27 September 2018

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27 September 2018

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27 September 2018

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27 September 2018

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Gene splicing by overlap extension

7 January 2021

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Keratocan-deficient mice display alterations in corneal structure

7 January 2021

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Retinal image quality in the rodent eye

7 January 2021

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10.1016/S0002-9440(10)63420-7

7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15509533%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15509533%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

15509533

1 reference