Fowler KJ - Search Results

1

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency.

McFarland R, Kirby DM, Fowler KJ, Ohtake A, Ryan MT, Amor DJ, Fletcher JM, Dixon JW, Collins FA, Turnbull DM, Taylor RW, Thorburn DR. McFarland R, et al. Among authors: fowler kj. Ann Neurol. 2004 Jan;55(1):58-64. doi: 10.1002/ana.10787. Ann Neurol. 2004. PMID: 14705112

2

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

Sarsero JP, Li L, Holloway TP, Voullaire L, Gazeas S, Fowler KJ, Kirby DM, Thorburn DR, Galle A, Cheema S, Koenig M, Williamson R, Ioannou PA. Sarsero JP, et al. Among authors: fowler kj. Mamm Genome. 2004 May;15(5):370-82. doi: 10.1007/s00335-004-3019-3. Mamm Genome. 2004. PMID: 15170226

3

Evaluation of an FRDA-EGFP genomic reporter assay in transgenic mice.

Sarsero JP, Holloway TP, Li L, McLenachan S, Fowler KJ, Bertoncello I, Voullaire L, Gazeas S, Ioannou PA. Sarsero JP, et al. Among authors: fowler kj. Mamm Genome. 2005 Apr;16(4):228-41. doi: 10.1007/s00335-004-3021-9. Mamm Genome. 2005. PMID: 15965784

4

A humanized BAC transgenic/knockout mouse model for HbE/beta-thalassemia.

Jamsai D, Zaibak F, Vadolas J, Voullaire L, Fowler KJ, Gazeas S, Peters H, Fucharoen S, Williamson R, Ioannou PA. Jamsai D, et al. Among authors: fowler kj. Genomics. 2006 Sep;88(3):309-15. doi: 10.1016/j.ygeno.2006.03.009. Epub 2006 May 2. Genomics. 2006. PMID: 16631345 Free article.

5

Transgenic mice expressing the Peripherin-EGFP genomic reporter display intrinsic peripheral nervous system fluorescence.

McLenachan S, Goldshmit Y, Fowler KJ, Voullaire L, Holloway TP, Turnley AM, Ioannou PA, Sarsero JP. McLenachan S, et al. Among authors: fowler kj. Transgenic Res. 2008 Dec;17(6):1103-16. doi: 10.1007/s11248-008-9210-7. Epub 2008 Aug 15. Transgenic Res. 2008. PMID: 18709437

6

A knock-out mouse model for methylmalonic aciduria resulting in neonatal lethality.

Peters H, Nefedov M, Sarsero J, Pitt J, Fowler KJ, Gazeas S, Kahler SG, Ioannou PA. Peters H, et al. Among authors: fowler kj. J Biol Chem. 2003 Dec 26;278(52):52909-13. doi: 10.1074/jbc.M310533200. Epub 2003 Oct 10. J Biol Chem. 2003. PMID: 14555645 Free article.

7

A humanized mouse model for a common beta0-thalassemia mutation.

Jamsai D, Zaibak F, Khongnium W, Vadolas J, Voullaire L, Fowler KJ, Gazeas S, Fucharoen S, Williamson R, Ioannou PA. Jamsai D, et al. Among authors: fowler kj. Genomics. 2005 Apr;85(4):453-61. doi: 10.1016/j.ygeno.2004.11.016. Genomics. 2005. PMID: 15780748

8

Uterine dysfunction and genetic modifiers in centromere protein B-deficient mice.

Fowler KJ, Hudson DF, Salamonsen LA, Edmondson SR, Earle E, Sibson MC, Choo KH. Fowler KJ, et al. Genome Res. 2000 Jan;10(1):30-41. Genome Res. 2000. PMID: 10645947 Free PMC article.

9

Analysis of mitotic and expression properties of human neocentromere-based transchromosomes in mice.

Wong LH, Saffery R, Anderson MA, Earle E, Quach JM, Stafford AJ, Fowler KJ, Choo KH. Wong LH, et al. Among authors: fowler kj. J Biol Chem. 2005 Feb 4;280(5):3954-62. doi: 10.1074/jbc.M410047200. Epub 2004 Nov 22. J Biol Chem. 2005. PMID: 15557333 Free article.

10

Spef1, a conserved novel testis protein found in mouse sperm flagella.

Chan SW, Fowler KJ, Choo KH, Kalitsis P. Chan SW, et al. Among authors: fowler kj. Gene. 2005 Jul 4;353(2):189-99. doi: 10.1016/j.gene.2005.04.025. Gene. 2005. PMID: 15979255

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