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M A Pook

Showing results (1-10 of 16) with videos related to

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Physiological Genomics|December 18, 2003
Defining a metabolic phenotype in the brain of a transgenic mouse model of spinocerebellar ataxia 3J L Griffin, C K Cemal, M A Pook
Human Immunology|November 1, 1991
Polymerase chain reaction analysis of transcriptional patterns of expression of class I HLA genesC W Summers, V Woodcock, M A Pook, 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.
Annals of Human Genetics|October 1, 1993
Localization of the Tamm-Horsfall glycoprotein (uromodulin) gene to chromosome 16p12.3-16p13.11M A Pook, S Jeremiah, S J Scheinman, et al.
The Journal of Clinical Investigation|June 1, 1993
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutationsR V Thakker, M A Pook, C Wooding, et al.
Human Molecular Genetics|December 1, 1993
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22M A Pook, O Wrong, C Wooding, et al.
Human Immunology|October 1, 1991
Characterization of an expressible nonclassical class I HLA geneM A Pook, V Woodcock, M Tassabehji, et al.
The Journal of Clinical Investigation|June 1, 1993
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesS J Scheinman, M A Pook, C Wooding, et al.
Gene Therapy|August 13, 2016
Lentivirus-meditated frataxin gene delivery reverses genome instability in Friedreich ataxia patient and mouse model fibroblastsH Khonsari, M Schneider, S Al-Mahdawi, 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.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Physiological Genomics|December 18, 2003
Defining a metabolic phenotype in the brain of a transgenic mouse model of spinocerebellar ataxia 3J L Griffin, C K Cemal, M A Pook
Human Immunology|November 1, 1991
Polymerase chain reaction analysis of transcriptional patterns of expression of class I HLA genesC W Summers, V Woodcock, M A Pook, 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.
Annals of Human Genetics|October 1, 1993
Localization of the Tamm-Horsfall glycoprotein (uromodulin) gene to chromosome 16p12.3-16p13.11M A Pook, S Jeremiah, S J Scheinman, et al.
The Journal of Clinical Investigation|June 1, 1993
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutationsR V Thakker, M A Pook, C Wooding, et al.
Human Molecular Genetics|December 1, 1993
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22M A Pook, O Wrong, C Wooding, et al.
Human Immunology|October 1, 1991
Characterization of an expressible nonclassical class I HLA geneM A Pook, V Woodcock, M Tassabehji, et al.
The Journal of Clinical Investigation|June 1, 1993
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesS J Scheinman, M A Pook, C Wooding, et al.
Gene Therapy|August 13, 2016
Lentivirus-meditated frataxin gene delivery reverses genome instability in Friedreich ataxia patient and mouse model fibroblastsH Khonsari, M Schneider, S Al-Mahdawi, 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.
Pageof 2