List of works - Fiona Mansergh

A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.

scientific article

Apoptosis gene profiling reveals spatio-temporal regulated expression of the p53/Mdm2 pathway during lens development

scientific article published on 11 February 2009

Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy.

scientific article published on 26 February 2014

Characterization and in silico mapping of a novel murine zinc finger transcription factor

scientific journal article

Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness

scientific article

Deficiency of SPARC suppresses intestinal tumorigenesis in APCMin/+ mice

scientific journal article

Developmentally regulated expression of hemoglobin subunits in avascular tissues

scientific article published in January 2008

ES cell neural differentiation reveals a substantial number of novel ESTs.

scientific article

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy

scientific article

Gene expression analysis of mouse embryonic stem cells following levitation in an ultrasound standing wave trap

scientific article

Gene expression changes during cataract progression in Sparc null mice: differential regulation of mouse globins in the lens.

scientific article

Gene expression changes during retinal development and rod specification

scientific article published on 20 January 2015

Gene expression profiles during early differentiation of mouse embryonic stem cells

scientific article

Gene therapies for inherited retinal disorders.

scientific article

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

scientific article

Novel mutations in the TIGR gene in early and late onset open angle glaucoma

article

Optimization of minuscule samples for use with cDNA microarrays

scientific article

Osteopenia in Sparc (osteonectin)-deficient mice: characterization of phenotypic determinants of femoral strength and changes in gene expression.

scientific article

RED: the analysis, management and dissemination of expressed sequence tags

scientific article published in December 2002

Reply

scientific article published in July 1996

Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

scientific article

Strategems in vitro for gene therapies directed to dominant mutations

article

Survivin expression is associated with lens epithelial cell proliferation and fiber cell differentiation.

scientific article published on 22 November 2012

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

scientific article published in January 1996

Three sequence polymorphisms in the PDC gene

article

List of works by Fiona Mansergh

A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.

Apoptosis gene profiling reveals spatio-temporal regulated expression of the p53/Mdm2 pathway during lens development

Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy.

Characterization and in silico mapping of a novel murine zinc finger transcription factor

Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness

Deficiency of SPARC suppresses intestinal tumorigenesis in APCMin/+ mice

Developmentally regulated expression of hemoglobin subunits in avascular tissues

ES cell neural differentiation reveals a substantial number of novel ESTs.

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy

Gene expression analysis of mouse embryonic stem cells following levitation in an ultrasound standing wave trap

Gene expression changes during cataract progression in Sparc null mice: differential regulation of mouse globins in the lens.

Gene expression changes during retinal development and rod specification

Gene expression profiles during early differentiation of mouse embryonic stem cells

Gene therapies for inherited retinal disorders.

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Novel mutations in the TIGR gene in early and late onset open angle glaucoma

Optimization of minuscule samples for use with cDNA microarrays

Osteopenia in Sparc (osteonectin)-deficient mice: characterization of phenotypic determinants of femoral strength and changes in gene expression.

RED: the analysis, management and dissemination of expressed sequence tags

Reply

Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

Strategems in vitro for gene therapies directed to dominant mutations

Survivin expression is associated with lens epithelial cell proliferation and fiber cell differentiation.

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

Three sequence polymorphisms in the PDC gene