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M A Morris

Showing results (121-130 of 152) with videos related to

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The Biochemical Journal|February 15, 1988
Effect of recombinant cytokines on glycolysis and fructose 2,6-bisphosphate in rheumatoid synovial cells in vitroD J Taylor, R J Whitehead, J M Evanson, et al.
American Journal of Human Genetics|August 1, 1995
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombinationJ L Blouin, D H Christie, A Gos, et al.
Pharmacology & Therapeutics|October 23, 2018
Role of the 12-lipoxygenase pathway in diabetes pathogenesis and complicationsA D Dobrian, M A Morris, D A Taylor-Fishwick, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
American Journal of Medical Genetics|May 15, 1994
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?A Bottani, W P Robinson, C D DeLozier-Blanchet, et al.
Annals of Internal Medicine|June 13, 1998
Clinical reporting to primary care physicians leads to increased use and understanding of bone densitometry and affects the management of osteoporosis. A randomized trialJ L Stock, C E Waud, J A Coderre, et al.
Italian Journal of Gastroenterology and Hepatology|June 24, 1999
Family linkage study of the T-cell receptor genes in coeliac diseaseJ Y Yiannakou, P M Brett, M A Morris, et al.
Scandinavian Journal of Gastroenterology|March 17, 2000
Coeliac disease and Down syndrome: associations not due to genetic linkage on chromosome 21M A Morris, J Y Yiannakou, A L King, et al.
Journal of Nanoscience and Nanotechnology|December 5, 2008
Mesoporous silicas impregnated with cobalt and nickel oxide nanoparticles and the growth of carbon nanotubes there fromD Barreca, W J Blau, F C Dillon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2008
Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlationC Djambas Khayat, N Salem, E Chouery, et al.
Pageof 16

Showing results (121-130 of 152) with videos related to

Sort By:
Pageof 16
The Biochemical Journal|February 15, 1988
Effect of recombinant cytokines on glycolysis and fructose 2,6-bisphosphate in rheumatoid synovial cells in vitroD J Taylor, R J Whitehead, J M Evanson, et al.
American Journal of Human Genetics|August 1, 1995
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombinationJ L Blouin, D H Christie, A Gos, et al.
Pharmacology & Therapeutics|October 23, 2018
Role of the 12-lipoxygenase pathway in diabetes pathogenesis and complicationsA D Dobrian, M A Morris, D A Taylor-Fishwick, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
American Journal of Medical Genetics|May 15, 1994
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?A Bottani, W P Robinson, C D DeLozier-Blanchet, et al.
Annals of Internal Medicine|June 13, 1998
Clinical reporting to primary care physicians leads to increased use and understanding of bone densitometry and affects the management of osteoporosis. A randomized trialJ L Stock, C E Waud, J A Coderre, et al.
Italian Journal of Gastroenterology and Hepatology|June 24, 1999
Family linkage study of the T-cell receptor genes in coeliac diseaseJ Y Yiannakou, P M Brett, M A Morris, et al.
Scandinavian Journal of Gastroenterology|March 17, 2000
Coeliac disease and Down syndrome: associations not due to genetic linkage on chromosome 21M A Morris, J Y Yiannakou, A L King, et al.
Journal of Nanoscience and Nanotechnology|December 5, 2008
Mesoporous silicas impregnated with cobalt and nickel oxide nanoparticles and the growth of carbon nanotubes there fromD Barreca, W J Blau, F C Dillon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2008
Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlationC Djambas Khayat, N Salem, E Chouery, et al.
Pageof 16