FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner (Q24293410)

Forkhead box C1

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Nuclear factor I A

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transcription factor binding

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author name string

Fred B Berry

1

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Megan A O'Neill

2

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Miguel Coca-Prados

3

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Michael A Walter

Molecular and Cellular Biology

4

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language of work or name

English

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publication date

February 2005

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published in

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volume

25

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issue

4

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page(s)

1415-24

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cites work

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19 March 2017

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FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain

19 March 2017

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The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis

19 March 2017

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A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

19 March 2017

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Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

19 March 2017

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The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH

19 March 2017

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Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

19 March 2017

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Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): a molecular leaf spring

19 March 2017

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Structure of HP1 chromodomain bound to a lysine 9-methylated histone H3 tail

19 March 2017

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Requirement for Pbx1 in skeletal patterning and programming chondrocyte proliferation and differentiation

19 March 2017

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A conformational change in PBX1A is necessary for its nuclear localization

19 March 2017

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The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus

19 March 2017

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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

19 March 2017

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Functional activity of myogenic HLH proteins requires hetero-oligomerization with E12/E47-like proteins in vivo

19 March 2017

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Subnuclear localization of C/EBP beta is regulated by growth hormone and dependent on MAPK

19 March 2017

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Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract

19 March 2017

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Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

19 March 2017

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The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye

19 March 2017

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Identification and Analysis of a Novel Mutation in the FOXC1 Forkhead Domain

19 March 2017

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Recovery from DNA damage-induced G2 arrest requires actin-binding protein filamin-A/actin-binding protein 280.

6 April 2017

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Fox's in development and disease

27 September 2017

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Filamin-A fragment localizes to the nucleus to regulate androgen receptor and coactivator functions

27 September 2017

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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

27 September 2017

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PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain.

27 September 2017

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Molecular genetics of Axenfeld-Rieger malformations

27 September 2017

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Interaction with BRCA2 suggests a role for filamin-1 (hsFLNa) in DNA damage response

27 September 2017

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Filamin associates with Smads and regulates transforming growth factor-beta signaling

27 September 2017

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Androgen receptor nuclear translocation is facilitated by the f-actin cross-linking protein filamin

27 September 2017

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Pbx-Hox heterodimers recruit coactivator-corepressor complexes in an isoform-specific manner

27 September 2017

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An Sp1-NF-Y/progesterone receptor DNA binding-dependent mechanism regulates progesterone-induced transcriptional activation of the rabbit RUSH/SMARCA3 gene

27 September 2017

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Actin-binding protein requirement for cortical stability and efficient locomotion

30 May 2018

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Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.

30 May 2018

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Forkhead genes and human disease

29 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/15684392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Interaction of p38 and Sp1 in a mechanical force-induced, beta 1 integrin-mediated transcriptional circuit that regulates the actin-binding protein filamin-A

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15684392