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R McInnes

Showing results (41-50 of 140) with videos related to

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Pathobiology Annual|January 1, 1981
Prolactin updateA E Mehta, G Tolis, C Goodyer, et al.
Acta Neuropathologica|January 1, 1992
"Reducing body"-like inclusions in skeletal muscle in childhood-onset acid maltase deficiencyV Jay, J Christodoulou, A Mercer-Connolly, et al.
Transactions of the American Ophthalmological Society|January 1, 1980
Treatment of gyrate atrophy of the choroid and retina with low arginine dietR R McInnes, S A Arshinoff, L Bell, et al.
Pediatrics|January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newbornR McInnes, P Lamm, C L Clow, et al.
Journal of the Canadian Dietetic Association|September 8, 1982
Use and design of low protein diets for children with inborn metabolic disordersL Bell, L Chan, W G Sherwood, et al.
Developmental Biology|May 27, 2009
Eye evolution at high resolution: the neuron as a unit of homologyTed Erclik, Volker Hartenstein, Roderick R McInnes, et al.
Current Biology : CB|August 30, 2008
Conserved role of the Vsx genes supports a monophyletic origin for bilaterian visual systemsTed Erclik, Volker Hartenstein, Howard D Lipshitz, et al.
The Journal of Pediatrics|March 1, 1993
Ornithine transcarbamylase deficiency presenting with strokelike episodesJ Christodoulou, I A Qureshi, R R McInnes, et al.
Human Molecular Genetics|July 1, 1994
Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine beta-synthase using an improved bacterial expression systemR de Franchis, V Kozich, R R McInnes, et al.
Journal of Medical Genetics|March 1, 1995
A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defectP M Smooker, J Christodoulou, R R McInnes, et al.
Pageof 14

Showing results (41-50 of 140) with videos related to

Sort By:
Pageof 14
Pathobiology Annual|January 1, 1981
Prolactin updateA E Mehta, G Tolis, C Goodyer, et al.
Acta Neuropathologica|January 1, 1992
"Reducing body"-like inclusions in skeletal muscle in childhood-onset acid maltase deficiencyV Jay, J Christodoulou, A Mercer-Connolly, et al.
Transactions of the American Ophthalmological Society|January 1, 1980
Treatment of gyrate atrophy of the choroid and retina with low arginine dietR R McInnes, S A Arshinoff, L Bell, et al.
Pediatrics|January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newbornR McInnes, P Lamm, C L Clow, et al.
Journal of the Canadian Dietetic Association|September 8, 1982
Use and design of low protein diets for children with inborn metabolic disordersL Bell, L Chan, W G Sherwood, et al.
Developmental Biology|May 27, 2009
Eye evolution at high resolution: the neuron as a unit of homologyTed Erclik, Volker Hartenstein, Roderick R McInnes, et al.
Current Biology : CB|August 30, 2008
Conserved role of the Vsx genes supports a monophyletic origin for bilaterian visual systemsTed Erclik, Volker Hartenstein, Howard D Lipshitz, et al.
The Journal of Pediatrics|March 1, 1993
Ornithine transcarbamylase deficiency presenting with strokelike episodesJ Christodoulou, I A Qureshi, R R McInnes, et al.
Human Molecular Genetics|July 1, 1994
Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine beta-synthase using an improved bacterial expression systemR de Franchis, V Kozich, R R McInnes, et al.
Journal of Medical Genetics|March 1, 1995
A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defectP M Smooker, J Christodoulou, R R McInnes, et al.
Pageof 14