Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1

Edmund Ui‐Hang Sim, Aaron G. Smith, Elida Szilagi, +4

Oncogene

GeneticsGene RegulationTumor SuppressorWnt-4 RegulationGene Expression +2

A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION

John Old, Shaheen N. Khan, Ishwar C. Verma, +11

Hemoglobin

Friedreich's Ataxia, No Changes in Mitochondrial Labile Iron in Human Lymphoblasts and Fibroblasts

Brigitte Sturm, Ute Bistrich, Matthias Schranzhofer, +6

Journal of Biological Chemistry

Upregulation of expression from the FRDA genomic locus for the therapy of Friedreich ataxia

Joseph P. Sarsero, Lingli Li, Hady Wardan, +3

The Journal of Gene Medicine

Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen

Jacques Puechberty, Anne‐Marie Laurent, Sylvie Gimenez, +8

Genomics

ChromatinPhysical AnalysesChromatin StructureGenetic DisorderNatural Sciences +13

Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice

Joseph P. Sarsero, Lingli Li, Timothy P. Holloway, +9

Mammalian Genome

Knockout MouseNeurodegenerative DiseasesGenetic DisorderGeneticsImmunology +4

Flow-cytometric analysis of mouse embryonic stem cell lipofection using small and large DNA constructs

Samuel McLenachan, Joseph P. Sarsero, Panos Ioannou

Genomics

Regenerative MedicineEmbryonic Stem CellInduced Pluripotent Stem CellDevelopmental BiologyMedicine +10

Pharmacological Screening Using an FXN-EGFP Cellular Genomic Reporter Assay for the Therapy of Friedreich Ataxia

Lingli Li, Lucille Voullaire, Chiranjeevi Sandi, +4

PLoS ONE

Neurodegenerative DiseasesMitochondrial BiogenesisMitochondrial FunctionGenetic DisorderMedicine +12

Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity

Kyproula Christodoulou, Feza Deymeer, Coşkun Özdemır, +6

Neurogenetics

Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsMolecular Biology +5

Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis

Panos Ioannou, George Christopoulos, Kyproula Panayides, +2

Neurology