F B Berry

Summary

Affiliation: University of Alberta
Country: Canada

Publications

  1. ncbi request reprint FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada
    J Biol Chem 277:10292-7. 2002
  2. pmc Initiation of early osteoblast differentiation events through the direct transcriptional regulation of Msx2 by FOXC1
    Farideh Mirzayans
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada
    PLoS ONE 7:e49095. 2012
  3. ncbi request reprint FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A
    Fred B Berry
    Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada
    Hum Mol Genet 17:490-505. 2008
  4. ncbi request reprint Regulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascade
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada
    J Biol Chem 281:10098-104. 2006
  5. ncbi request reprint Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta, Canada, T6G 2H7
    Hum Mol Genet 15:905-19. 2006
  6. ncbi request reprint The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta, Canada T6G 2H7
    Hum Mol Genet 14:2619-27. 2005
  7. pmc FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, AB, Canada
    Mol Cell Biol 25:1415-24. 2005
  8. ncbi request reprint Positive and negative regulation of myogenic differentiation of C2C12 cells by isoforms of the multiple homeodomain zinc finger transcription factor ATBF1
    F B Berry
    Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta T2N 4N1, Canada
    J Biol Chem 276:25057-65. 2001
  9. ncbi request reprint Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
    Ramsey A Saleem
    Department of Human Genetics, University of Alberta, Edmonton, Canada, T6G 2H7
    Hum Mol Genet 12:2993-3005. 2003
  10. doi request reprint Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cells
    Lijia Huang
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada
    Invest Ophthalmol Vis Sci 49:5243-9. 2008

Collaborators

Detail Information

Publications13

  1. ncbi request reprint FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada
    J Biol Chem 277:10292-7. 2002
    ..These results indicate that FOXC1 is under complex regulatory control with multiple functional domains modulating FOXC1 transcriptional regulation...
  2. pmc Initiation of early osteoblast differentiation events through the direct transcriptional regulation of Msx2 by FOXC1
    Farideh Mirzayans
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada
    PLoS ONE 7:e49095. 2012
    ..Together these findings suggest that a Foxc1->Msx2 regulatory network functions in the initial stages of osteoblast differentiation...
  3. ncbi request reprint FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A
    Fred B Berry
    Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada
    Hum Mol Genet 17:490-505. 2008
    ....
  4. ncbi request reprint Regulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascade
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada
    J Biol Chem 281:10098-104. 2006
    ..These results indicate that FOXC1 protein levels and activity are tightly regulated by post-translational modifications...
  5. ncbi request reprint Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta, Canada, T6G 2H7
    Hum Mol Genet 15:905-19. 2006
    ..Our findings indicate that the functional interaction between FOXC1 and PITX2A underlies the sensitivity to FOXC1 gene dosage in Axenfeld-Rieger syndrome and related anterior segment dysgeneses...
  6. ncbi request reprint The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, Alberta, Canada T6G 2H7
    Hum Mol Genet 14:2619-27. 2005
    ..Together, these data indicate that these FOXC2 missense mutations are functional nulls and that FOXC2 haploinsufficiency underlies hereditary LD and validates the predictive ability of the FOXC1-based FHD mutational model...
  7. pmc FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner
    Fred B Berry
    Department of Ophthalmology, University of Alberta, Edmonton, AB, Canada
    Mol Cell Biol 25:1415-24. 2005
    ....
  8. ncbi request reprint Positive and negative regulation of myogenic differentiation of C2C12 cells by isoforms of the multiple homeodomain zinc finger transcription factor ATBF1
    F B Berry
    Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta T2N 4N1, Canada
    J Biol Chem 276:25057-65. 2001
    ..These results suggest that ATBF1-A plays a role in the maintenance of the undifferentiated myoblast state, and its down-regulation is a prerequisite to initiate terminal differentiation of C2C12 cells...
  9. ncbi request reprint Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
    Ramsey A Saleem
    Department of Human Genetics, University of Alberta, Edmonton, Canada, T6G 2H7
    Hum Mol Genet 12:2993-3005. 2003
    ..Importantly, these results can also be applied to predict the consequences of the molecular effects of mutations of other FOX genes that have analogous missense mutations, including FOXP2, FOXE3 and FOXC2...
  10. doi request reprint Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cells
    Lijia Huang
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada
    Invest Ophthalmol Vis Sci 49:5243-9. 2008
    ..Understanding the function of FOXC1 necessitates characterizing the proteins that interact with FOXC1. This study was undertaken to isolate FOXC1-interacting proteins and determine their effects on FOXC1...
  11. ncbi request reprint Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia
    Yoko A Ito
    Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada
    Invest Ophthalmol Vis Sci 50:3573-9. 2009
    ..A novel FOXC1 W152G mutation was identified in a patient with aniridia. Molecular analysis was conducted to determine the functional consequences of the FOXC1 W152G mutation...
  12. pmc Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1
    R A Saleem
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, T6G 2H7, Canada
    Am J Hum Genet 68:627-41. 2001
    ..In addition, these findings demonstrate that reduced stability, DNA binding, or transactivation, all causing a decrease in the ability of FOXC1 to transactivate genes, can underlie AR malformations...
  13. ncbi request reprint FGF19 is a target for FOXC1 regulation in ciliary body-derived cells
    Yahya Tamimi
    Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada
    Hum Mol Genet 15:3229-40. 2006
    ..This study reveals an important role for FOXC1 in the direct regulation of the FGF19-FGFR4-MAPK pathway to promote both the development and maintenance of anterior segment structures within the eye...