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K Doudney

Showing results (1-10 of 12) with videos related to

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Human Molecular Genetics|November 16, 2001
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specificationJ N Murdoch, K Doudney, C Paternotte, et al.
Genomics|May 15, 1997
Exon-intron structure of a 2.7-kb transcript of the STM7 gene with phosphatidylinositol-4-phosphate 5-kinase activityM A Pook, J J Carvajal, K Doudney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
A family with pseudodominant Friedreich's ataxia showing marked variation of phenotype between affected siblingsS Webb, K Doudney, M Pook, et al.
Genomics|June 13, 2001
Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23K Doudney, J N Murdoch, C Paternotte, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5R Hillermann, C G See, M Pook, et al.
The Pharmacogenomics Journal|March 11, 2015
Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producersE W Chua, S Cree, M L Barclay, et al.
Human Molecular Genetics|August 1, 1995
Friedreich's ataxia: a defect in signal transduction?J J Carvajal, M A Pook, K Doudney, et al.
American Journal of Human Genetics|January 1, 1993
Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9qS Chamberlain, M Farrall, J Shaw, et al.
Journal of Dental Research|January 1, 2010
Autosomal-dominant ankyloglossia and tooth number anomaliesA C Acevedo, J A C da Fonseca, J Grinham, et al.
Acta Neuropsychiatrica|March 9, 2016
Upstream genetic variant near INSIG2, influences response to carnitine supplementation in bipolar patients with valproate-induced weight gainK Doudney, J A Harley, J F Pearson, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|November 16, 2001
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specificationJ N Murdoch, K Doudney, C Paternotte, et al.
Genomics|May 15, 1997
Exon-intron structure of a 2.7-kb transcript of the STM7 gene with phosphatidylinositol-4-phosphate 5-kinase activityM A Pook, J J Carvajal, K Doudney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
A family with pseudodominant Friedreich's ataxia showing marked variation of phenotype between affected siblingsS Webb, K Doudney, M Pook, et al.
Genomics|June 13, 2001
Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23K Doudney, J N Murdoch, C Paternotte, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5R Hillermann, C G See, M Pook, et al.
The Pharmacogenomics Journal|March 11, 2015
Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producersE W Chua, S Cree, M L Barclay, et al.
Human Molecular Genetics|August 1, 1995
Friedreich's ataxia: a defect in signal transduction?J J Carvajal, M A Pook, K Doudney, et al.
American Journal of Human Genetics|January 1, 1993
Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9qS Chamberlain, M Farrall, J Shaw, et al.
Journal of Dental Research|January 1, 2010
Autosomal-dominant ankyloglossia and tooth number anomaliesA C Acevedo, J A C da Fonseca, J Grinham, et al.
Acta Neuropsychiatrica|March 9, 2016
Upstream genetic variant near INSIG2, influences response to carnitine supplementation in bipolar patients with valproate-induced weight gainK Doudney, J A Harley, J F Pearson, et al.
Pageof 2