A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis (2008)
Martin, Dianna C., Atmuri, V., Hemming, R. J., Farley, J., Mort, J. S., Byers, Sharon, ...
Copyright © The Author 2008. Published by Oxford University Press. All rights reserved.
A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis (2008)
Martin, Dianna C., Atmuri, V., Hemming, R. J., Farley, J., Mort, J. S., Byers, Sharon, ...
Copyright © The Author 2008. Published by Oxford University Press. All rights reserved.
Nucleotide sequence of katG, encoding catalase HPI of Escherichia coli.
Triggs-Raine, B L, Doble, B W, Mulvey, M R, Sorby, P A, Loewen, P C
The gene katG, encoding catalase HPI of Escherichia coli, was sequenced, predicting a 726-amino-acid protein. The sequence was confirmed by identification of potential regulatory elements and amino...
Cao, Z, Natowicz, M R, Kaback, M M, Lim-Steele, J S, Prence, E M, Brown, D, ...
Deficient activity of beta-hexosaminidase A (Hex A), resulting from mutations in the HEXA gene, typically causes Tay-Sachs disease. However, healthy individuals lacking Hex A activity against...
Triggs-Raine, B. L., Mules, E. H., Kaback, M. M., Dowling, C. E., Akerman, B. R., ...
Deficiency of β-hexosaminidase A (Hex A) activity typically results in Tay-Sachs disease. However, healthy subjects found to be deficient in Hex A activity (i.e., pseudodeficient) by means of in...
Triggs-Raine, B L, Akerman, B R, Clarke, J T, Gravel, R A
The rapid identification of mutations causing Tay-Sachs disease requires the capacity to readily screen the regions of the HEXA gene most likely to be affected by mutation. We have sequenced the...
Nucleotide sequence of katG, encoding catalase HPI of Escherichia coli.
Triggs-Raine, B L, Doble, B W, Mulvey, M R, Sorby, P A, Loewen, P C
The gene katG, encoding catalase HPI of Escherichia coli, was sequenced, predicting a 726-amino-acid protein. The sequence was confirmed by identification of potential regulatory elements and amino...
Cao, Z, Natowicz, M R, Kaback, M M, Lim-Steele, J S, Prence, E M, Brown, D, ...
Deficient activity of beta-hexosaminidase A (Hex A), resulting from mutations in the HEXA gene, typically causes Tay-Sachs disease. However, healthy individuals lacking Hex A activity against...
Triggs-Raine, B. L., Mules, E. H., Kaback, M. M., Dowling, C. E., Akerman, B. R., ...
Deficiency of β-hexosaminidase A (Hex A) activity typically results in Tay-Sachs disease. However, healthy subjects found to be deficient in Hex A activity (i.e., pseudodeficient) by means of in...
Triggs-Raine, B L, Akerman, B R, Clarke, J T, Gravel, R A
The rapid identification of mutations causing Tay-Sachs disease requires the capacity to readily screen the regions of the HEXA gene most likely to be affected by mutation. We have sequenced the...