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M Z Jones

Showing results (31-40 of 74) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1984
Beta-mannosidosis: prenatal biochemical and morphological characteristicsM Z Jones, E J Rathke, K Cavanagh, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Molecular defect of caprine N-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5'-region of the coding sequenceK T Cavanagh, J R Leipprandt, M Z Jones, et al.
Muscle & Nerve|March 1, 1978
Becker-type muscular dystrophyW G Bradley, M Z Jones, J M Mussini, et al.
Acta Neuropathologica|April 12, 1979
Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by BeckerH H Goebel, H Prange, F Gullotta, et al.
Theriogenology|September 1, 1995
Development and efficacy of ultrasound-guided fetal fluid aspiration techniques for prenatal diagnosis of caprine beta-mannosidosisK L Lovell, D J Sprecher, N K Ames, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Thyroid structure and function in bovine beta-mannosidosisK L Lovell, M Z Jones, J Patterson, et al.
Brain Research|June 30, 1978
A histological study of kainic acid-induced lesions in the rat brainS M Wuerthele, K L Lovell, M Z Jones, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Beta-mannosidosis: prenatal detection of caprine allantoic fluid oligosaccharides with thin layer, gel permeation and high performance liquid chromatographyD L Dahl, C D Warren, E J Rathke, et al.
Veterinary Pathology|September 1, 1989
Ocular pathology of caprine beta-mannosidosisJ A Render, K L Lovell, M Z Jones, et al.
Molecular Genetics and Metabolism|March 13, 2001
Metabolic studies of glycosphingolipid accumulation in mucopolysaccharidosis IIIDS S Liour, M Z Jones, M Suzuki, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Journal of Inherited Metabolic Disease|January 1, 1984
Beta-mannosidosis: prenatal biochemical and morphological characteristicsM Z Jones, E J Rathke, K Cavanagh, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Molecular defect of caprine N-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5'-region of the coding sequenceK T Cavanagh, J R Leipprandt, M Z Jones, et al.
Muscle & Nerve|March 1, 1978
Becker-type muscular dystrophyW G Bradley, M Z Jones, J M Mussini, et al.
Acta Neuropathologica|April 12, 1979
Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by BeckerH H Goebel, H Prange, F Gullotta, et al.
Theriogenology|September 1, 1995
Development and efficacy of ultrasound-guided fetal fluid aspiration techniques for prenatal diagnosis of caprine beta-mannosidosisK L Lovell, D J Sprecher, N K Ames, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Thyroid structure and function in bovine beta-mannosidosisK L Lovell, M Z Jones, J Patterson, et al.
Brain Research|June 30, 1978
A histological study of kainic acid-induced lesions in the rat brainS M Wuerthele, K L Lovell, M Z Jones, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Beta-mannosidosis: prenatal detection of caprine allantoic fluid oligosaccharides with thin layer, gel permeation and high performance liquid chromatographyD L Dahl, C D Warren, E J Rathke, et al.
Veterinary Pathology|September 1, 1989
Ocular pathology of caprine beta-mannosidosisJ A Render, K L Lovell, M Z Jones, et al.
Molecular Genetics and Metabolism|March 13, 2001
Metabolic studies of glycosphingolipid accumulation in mucopolysaccharidosis IIIDS S Liour, M Z Jones, M Suzuki, et al.
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