Kerry J Fowler
Overview
Explore the profile of Kerry J Fowler including associated specialties, affiliations and a list of published articles.
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12
Citations
257
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Recent Articles
1.
McLenachan S, Goldshmit Y, Fowler K, Voullaire L, Holloway T, Turnley A, et al.
Transgenic Res
. 2008 Aug;
17(6):1103-16.
PMID: 18709437
The development of homologous recombination methods for the precise modification of bacterial artificial chromosomes has allowed the introduction of disease causing mutations or fluorescent reporter genes into human loci for...
2.
Jamsai D, Zaibak F, Vadolas J, Voullaire L, Fowler K, Gazeas S, et al.
Genomics
. 2006 Apr;
88(3):309-15.
PMID: 16631345
Hemoglobin E (HbE) is caused by a G-->A mutation at codon 26 of the beta-globin gene, which substitutes Glu-->Lys. This mutation gives rise to functional but unstable hemoglobin and activates...
3.
Chan S, Fowler K, Choo K, Kalitsis P
Gene
. 2005 Jun;
353(2):189-99.
PMID: 15979255
We describe the cloning and characterisation of Spef1, a novel testis-specific gene. Spef1 has evolutionary orthologues in a wide range of species including mammals, other vertebrates, Drosophila, and protozoans with...
4.
Sarsero J, Holloway T, Li L, McLenachan S, Fowler K, Bertoncello I, et al.
Mamm Genome
. 2005 Jun;
16(4):228-41.
PMID: 15965784
Friedreich ataxia is an autosomal recessive neurodegenerative disorder caused by a GAA trinucleotide expansion in the first intron of the Friedreich ataxia gene (FRDA) that causes reduced synthesis of frataxin,...
5.
Kalitsis P, Fowler K, Griffiths B, Earle E, Chow C, Jamsen K, et al.
Genes Chromosomes Cancer
. 2005 May;
44(1):29-36.
PMID: 15898111
Mitotic spindle checkpoint proteins have been shown to play a crucial role in the accurate segregation of chromosomes during cell division. Bub3 is a member of a group of mitotic...
6.
7.
Jamsai D, Zaibak F, Khongnium W, Vadolas J, Voullaire L, Fowler K, et al.
Genomics
. 2005 Mar;
85(4):453-61.
PMID: 15780748
Accurate animal models that recapitulate the phenotype and genotype of patients with beta-thalassemia would enable the development of a range of possible therapeutic approaches. Here we report the generation of...
8.
Wong L, Saffery R, Anderson M, Earle E, Quach J, Stafford A, et al.
J Biol Chem
. 2004 Nov;
280(5):3954-62.
PMID: 15557333
Human neocentromeres are functional centromeres that are devoid of the typical human centromeric alpha-satellite DNA. We have transferred a 60-Mb chromosome 10-derived neocentric marker chromosome, mardel(10), and its truncated 3.5-Mb...
9.
Sarsero J, Li L, Holloway T, Voullaire L, Gazeas S, Fowler K, et al.
Mamm Genome
. 2004 Jun;
15(5):370-82.
PMID: 15170226
Three independent transgenic mouse lines were generated with the human Friedreich ataxia gene, FRDA, in an 188-kb bacterial artificial chromosome (BAC) genomic sequence. Three copies of the transgene per diploid...
10.
McFarland R, Kirby D, Fowler K, Ohtake A, Ryan M, Amor D, et al.
Ann Neurol
. 2004 Jan;
55(1):58-64.
PMID: 14705112
Both nuclear and mitochondrial DNA mutations can cause energy generation disorders. Respiratory chain complex I deficiency is the most common energy generation disorder and a frequent cause of infantile mitochondrial...