Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation

G. Bruce Mann, Kerry J. Fowler, Anastasia Gabriel, +3

Cell

Skin DevelopmentDevelopmental BiologyOphthalmologyCorneal DystrophyCutaneous Biology +6

Survivin and the inner centromere protein INCENP show similar cell-cycle localization and gene knockout phenotype

Anthony G. Uren, Lee H. Wong, Miha Pakusch, +4

Current Biology

ChromatinChromosome DynamicsCell DivisionGene Knockout PhenotypeGenetics +9

Early disruption of centromeric chromatin organization in centromere protein A (<i>Cenpa</i>) null mice

Emily V. Howman, Kerry J. Fowler, Ainsley J. Newson, +4

Proceedings of the National Academy of Sciences

Null MiceEpigenetic ChangeGeneticsCell CycleCentromeric Chromatin +19

<i>Bub3</i> gene disruption in mice reveals essential mitotic spindle checkpoint function during early embryogenesis

Paul Kalitsis, Elizabeth D. Earle, Kerry J. Fowler, +1

Genes & Development

GeneticsCell CycleChromatin BridgingCell RegulationNull Embryos +16

Centromere Protein B Null Mice are Mitotically and Meiotically Normal but Have Lower Body and Testis Weights

Damien F. Hudson, Kerry J. Fowler, Elizabeth D. Earle, +12

The Journal of Cell Biology

SpermatogenesisCytogeneticsGeneticsMolecular GeneticsReproductive Biology +17

A mutation in the epidermal growth factor receptor in waved-2 mice has a profound effect on receptor biochemistry that results in impaired lactation.

Kerry J. Fowler, Francesca Walker, Warren S. Alexander, +7

Proceedings of the National Academy of Sciences

De novo mutations in the mitochondrial <i>ND3</i> gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

Robert McFarland, Denise M. Kirby, Kerry J. Fowler, +9

Annals of Neurology

Infantile Mitochondrial EncephalopathyGeneticsMolecular BiologyNuclear Gene DefectsMolecular Genetics +15

Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo death

Paul Kalitsis, Kerry J. Fowler, Elizabeth D. Earle, +2

Proceedings of the National Academy of Sciences

CytogeneticsGeneticsEarly Embryo DeathMolecular GeneticsEpigenetics +18

Neutralizing monoclonal antibodies to human rotavirus and indications of antigenic drift among strains from neonates

Barbara S. Coulson, Kerry J. Fowler, Ruth F. Bishop, +1

Journal of Virology

Viral DiagnosticsImmunologyViral PathogenesisSerotype 3Viral Structural Protein +15

β-Hydroxyisobutyryl Coenzyme A Deacylase Deficiency: A Defect in Valine Metabolism Associated with Physical Malformations

Garry K. Brown, Susan M. Hunt, R. D. Scholem, +7

PEDIATRICS

BiochemistryNatural SciencesMetabolic DiseasePhysiologyInherited Metabolic Disease +13