about
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retinaDeficiency of SPARC suppresses intestinal tumorigenesis in APCMin/+ miceCharacterization and in silico mapping of a novel murine zinc finger transcription factorGene expression analysis of mouse embryonic stem cells following levitation in an ultrasound standing wave trap.ES cell neural differentiation reveals a substantial number of novel ESTs.Optimization of minuscule samples for use with cDNA microarrays.Gene expression profiles during early differentiation of mouse embryonic stem cells.Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.Apoptosis gene profiling reveals spatio-temporal regulated expression of the p53/Mdm2 pathway during lens developmentGene therapies for inherited retinal disorders.Gene expression changes during retinal development and rod specification.Gene expression changes during cataract progression in Sparc null mice: differential regulation of mouse globins in the lens.Survivin expression is associated with lens epithelial cell proliferation and fiber cell differentiation.Osteopenia in Sparc (osteonectin)-deficient mice: characterization of phenotypic determinants of femoral strength and changes in gene expression.Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy.Developmentally regulated expression of hemoglobin subunits in avascular tissues.Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland.RED: the analysis, management and dissemination of expressed sequence tags.Strategems in vitro for gene therapies directed to dominant mutationsThree sequence polymorphisms in the PDC geneNovel mutations in the TIGR gene in early and late onset open angle glaucomaReply
P50
Q28271659-1E8C9A63-0A88-4686-9CFB-2F6505980934Q28505216-6AC1C4C6-551E-4400-9A5F-3D418583CE73Q28585424-568F60D8-3C1A-45BA-B98A-05251AD6DFCAQ30476418-62C624E8-F7CB-4498-9A0C-F24EFFF31347Q32059426-8D3B99EB-D1EA-4EB3-9C9D-388DC432F7FDQ33318996-5D6570D0-A783-4F96-838E-365DC52F82CFQ33398806-2F358ED6-02CD-4DFD-A592-74628802584CQ33682728-E8AA6087-0EA2-426C-9207-28B3B7C2B5B9Q34306058-846E114B-5C8C-442C-BF80-F9F75E2AECBFQ34389296-C1B4FDAC-E536-4EBD-AB44-8763331A6B2EQ35299420-D46832A3-2F35-4AE0-82DC-DE5B8F01F109Q37251881-C6099904-3FC7-41EE-B62A-244CE0AED481Q38221905-9BEB2608-4ECE-4397-B6DE-9E6C8AE9E5EBQ38301080-00F35457-57BC-4604-AF15-1D1A91A1C392Q38337956-412B0A8E-E52E-4472-98DB-431D11FD0EEEQ41944319-7AC56FE9-A15C-4E77-ABFB-5B04BAF95256Q42070862-A197FE19-1880-4537-BDF5-8C9D81435B89Q42235259-43D425EA-9061-4EC5-853C-1FF9210E0B74Q46290555-725A19ED-0E44-455A-8654-0F1952E3A01EQ48067489-31B733DC-0D56-45A0-B9ED-FEFC7809D082Q48268776-0FF24683-A8C3-4B5E-AB1F-47AA5C89E337Q60653034-8329A8DF-C172-4EB3-893F-86DEA05D318AQ60653050-F3329CB6-3788-40C0-9C92-66200B73F776Q74376898-D851E0F8-07A2-44A1-B0E2-B395B740E90CQ93601547-833147AF-B3BC-4DF1-BBE5-CC377428B013
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fiona Mansergh
@ast
Fiona Mansergh
@en
Fiona Mansergh
@es
Fiona Mansergh
@nl
Fiona Mansergh
@sl
type
label
Fiona Mansergh
@ast
Fiona Mansergh
@en
Fiona Mansergh
@es
Fiona Mansergh
@nl
Fiona Mansergh
@sl
prefLabel
Fiona Mansergh
@ast
Fiona Mansergh
@en
Fiona Mansergh
@es
Fiona Mansergh
@nl
Fiona Mansergh
@sl
P106
P1153
6603578145
P21
P31
P496
0000-0001-7763-0383