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Diane W Cox

Showing results (1-10 of 22) with videos related to

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Human Genetics|October 28, 2003
A comparison of the mutation spectra of Menkes disease and Wilson diseaseGloria Hsi, Diane W Cox
Human Mutation|August 8, 2007
Sequence variation database for the Wilson disease copper transporter, ATP7BSusan M Kenney, Diane W Cox
Journal of Bioenergetics and Biomembranes|January 24, 2003
Copper transporting P-type ATPases and human diseaseDiane W Cox, Steven D P Moore
Nephron|October 10, 2002
Expression in mouse kidney of membrane copper transporters Atp7a and Atp7bSteven D P Moore, Diane W Cox
American Journal of Medical Genetics. Part A|April 15, 2009
A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlationsKamilla Schlade-Bartusiak, Holly Ardinger, Diane W Cox
Genetic Testing|April 1, 2008
New mutations in the Wilson disease gene, ATP7B: implications for molecular testingLisa Prat Davies, Georgina Macintyre, Diane W Cox
Journal of Hepatology|July 17, 2007
Three atypical cases of Wilson disease: assessment of the Leipzig scoring system in making a diagnosisAndy Xuan, Ian Bookman, Diane W Cox, et al.
Veterinary Journal (London, England : 1997)|June 19, 2007
Polymorphisms in canine ATP7B: candidate modifier of copper toxicosis in the Bedlington terrierVeronica A Coronado, Brian O'Neill, Manoj Nanji, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
A child with deletion (14)(q24.3q32.13) and auditory neuropathyKamilla Schlade-Bartusiak, Georgina Macintyre, Janice Zunich, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 20, 2003
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosisVeronica A Coronado, Deepti Damaraju, Ritva Kohijoki, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Human Genetics|October 28, 2003
A comparison of the mutation spectra of Menkes disease and Wilson diseaseGloria Hsi, Diane W Cox
Human Mutation|August 8, 2007
Sequence variation database for the Wilson disease copper transporter, ATP7BSusan M Kenney, Diane W Cox
Journal of Bioenergetics and Biomembranes|January 24, 2003
Copper transporting P-type ATPases and human diseaseDiane W Cox, Steven D P Moore
Nephron|October 10, 2002
Expression in mouse kidney of membrane copper transporters Atp7a and Atp7bSteven D P Moore, Diane W Cox
American Journal of Medical Genetics. Part A|April 15, 2009
A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlationsKamilla Schlade-Bartusiak, Holly Ardinger, Diane W Cox
Genetic Testing|April 1, 2008
New mutations in the Wilson disease gene, ATP7B: implications for molecular testingLisa Prat Davies, Georgina Macintyre, Diane W Cox
Journal of Hepatology|July 17, 2007
Three atypical cases of Wilson disease: assessment of the Leipzig scoring system in making a diagnosisAndy Xuan, Ian Bookman, Diane W Cox, et al.
Veterinary Journal (London, England : 1997)|June 19, 2007
Polymorphisms in canine ATP7B: candidate modifier of copper toxicosis in the Bedlington terrierVeronica A Coronado, Brian O'Neill, Manoj Nanji, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
A child with deletion (14)(q24.3q32.13) and auditory neuropathyKamilla Schlade-Bartusiak, Georgina Macintyre, Janice Zunich, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 20, 2003
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosisVeronica A Coronado, Deepti Damaraju, Ritva Kohijoki, et al.
Pageof 3