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M B Coulter

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Kidney International|November 30, 2006
4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?M B Coulter-Mackie
Molecular Genetics and Metabolism|September 15, 2006
Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutationsM B Coulter-Mackie, Q Lian
Molecular Genetics and Metabolism|May 2, 2008
Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutantsM B Coulter-Mackie, Q Lian
American Journal of Human Genetics|October 1, 1992
A double mutation in exon 6 of the beta-hexosaminidase alpha subunit in a patient with the B1 variant of Tay-Sachs diseaseP J Ainsworth, M B Coulter-Mackie
Virus Research|September 1, 1984
In vivo and in vitro models of demyelinating disease X. A Schwannoma-L-2 somatic cell hybrid persistently yielding high titres of mouse hepatitis virus strain JHMM B Coulter-Mackie, W F Flintoff, S Dales
Virology|September 1, 1984
In vivo and in vitro models of demyelinating disease. IX. Progression of JHM virus infection in the central nervous system of the rat during overt and asymptomatic phasesO Sorensen, M B Coulter-Mackie, S Puchalski, et al.
Human Molecular Genetics|April 1, 1993
Evidence of DNA methylation in the neurofibromatosis type 1 (NF1) gene region of 17q11.2D I Rodenhiser, M B Coulter-Mackie, S M Singh
Clinical Biochemistry|February 1, 1997
DNA-based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay: a case in pointM B Coulter-Mackie, D A Applegarth, J Toone, et al.
Clinical Biochemistry|January 7, 1999
A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletionM B Coulter-Mackie, D A Applegarth, J R Toone, et al.
Molecular Genetics and Metabolism|November 16, 2001
Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluriaM B Coulter-Mackie, G Rumsby, D A Applegarth, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Kidney International|November 30, 2006
4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?M B Coulter-Mackie
Molecular Genetics and Metabolism|September 15, 2006
Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutationsM B Coulter-Mackie, Q Lian
Molecular Genetics and Metabolism|May 2, 2008
Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutantsM B Coulter-Mackie, Q Lian
American Journal of Human Genetics|October 1, 1992
A double mutation in exon 6 of the beta-hexosaminidase alpha subunit in a patient with the B1 variant of Tay-Sachs diseaseP J Ainsworth, M B Coulter-Mackie
Virus Research|September 1, 1984
In vivo and in vitro models of demyelinating disease X. A Schwannoma-L-2 somatic cell hybrid persistently yielding high titres of mouse hepatitis virus strain JHMM B Coulter-Mackie, W F Flintoff, S Dales
Virology|September 1, 1984
In vivo and in vitro models of demyelinating disease. IX. Progression of JHM virus infection in the central nervous system of the rat during overt and asymptomatic phasesO Sorensen, M B Coulter-Mackie, S Puchalski, et al.
Human Molecular Genetics|April 1, 1993
Evidence of DNA methylation in the neurofibromatosis type 1 (NF1) gene region of 17q11.2D I Rodenhiser, M B Coulter-Mackie, S M Singh
Clinical Biochemistry|February 1, 1997
DNA-based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay: a case in pointM B Coulter-Mackie, D A Applegarth, J Toone, et al.
Clinical Biochemistry|January 7, 1999
A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletionM B Coulter-Mackie, D A Applegarth, J R Toone, et al.
Molecular Genetics and Metabolism|November 16, 2001
Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluriaM B Coulter-Mackie, G Rumsby, D A Applegarth, et al.
Pageof 2