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J A Lowden

Showing results (71-80 of 80) with videos related to

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Pediatric Radiology|January 1, 1983
Biliary disease in metachromatic leukodystrophyL Heier, A Daneman, J A Lowden, et al.
Research Communications in Chemical Pathology and Pharmacology|July 1, 1983
Stability of the paraoxonase phenotyping ratio in collections of human sera with differing storage timesM Brackley, G Carro-Ciampi, D J Stewart, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
American Journal of Human Genetics|November 1, 1979
Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharidesR A Gravel, J A Lowden, J W Callahan, et al.
American Journal of Human Genetics|January 1, 1978
Carrier detection in Sandhoff diseaseJ A Lowden, E J Ives, D L Keene, et al.
The Journal of Biological Chemistry|September 25, 1986
Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)B F O'Dowd, M H Klavins, H F Willard, et al.
American Journal of Obstetrics and Gynecology|February 1, 1974
The antenatal diagnosis of genetic diseaseT A Doran, N L Rudd, H A Gardner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidaseB F O'Dowd, F Quan, H F Willard, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
The Journal of Biological Chemistry|June 25, 1986
Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs diseaseR G Korneluk, D J Mahuran, K Neote, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Pediatric Radiology|January 1, 1983
Biliary disease in metachromatic leukodystrophyL Heier, A Daneman, J A Lowden, et al.
Research Communications in Chemical Pathology and Pharmacology|July 1, 1983
Stability of the paraoxonase phenotyping ratio in collections of human sera with differing storage timesM Brackley, G Carro-Ciampi, D J Stewart, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
American Journal of Human Genetics|November 1, 1979
Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharidesR A Gravel, J A Lowden, J W Callahan, et al.
American Journal of Human Genetics|January 1, 1978
Carrier detection in Sandhoff diseaseJ A Lowden, E J Ives, D L Keene, et al.
The Journal of Biological Chemistry|September 25, 1986
Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)B F O'Dowd, M H Klavins, H F Willard, et al.
American Journal of Obstetrics and Gynecology|February 1, 1974
The antenatal diagnosis of genetic diseaseT A Doran, N L Rudd, H A Gardner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidaseB F O'Dowd, F Quan, H F Willard, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
The Journal of Biological Chemistry|June 25, 1986
Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs diseaseR G Korneluk, D J Mahuran, K Neote, et al.
Pageof 8