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The New England Journal of Medicine
|
August 10, 1995
Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene
J Walston, K Silver, C Bogardus, et al.
American Journal of Medical Genetics
|
September 17, 1998
Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease
F Martiniuk, A Chen, A Mack, et al.
Human Molecular Genetics
|
October 9, 2001
Conditional tissue-specific expression of the acid alpha-glucosidase (GAA) gene in the GAA knockout mice: implications for therapy
N Raben, N Lu, K Nagaraju, et al.
Neurology
|
June 27, 2001
Surprises of genetic engineering: a possible model of polyglucosan body disease
N Raben, M Danon, N Lu, et al.
Human Gene Therapy
|
March 27, 2001
Intercellular transfer of the virally derived precursor form of acid alpha-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy Pompe disease
D F Pauly, T J Fraites, C Toma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 2, 2000
Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies
K Nagaraju, N Raben, L Loeffler, et al.
Diabetes/Metabolism Research and Reviews
|
October 12, 2000
Molecular scanning for mutations in the insulin receptor substrate-1 (IRS-1) gene in Mexican Americans with Type 2 diabetes mellitus
F S Celi, C Negri, K Tanner, et al.
Molecular Genetics and Metabolism
|
June 10, 2008
Biochemical and pharmacological characterization of different recombinant acid alpha-glucosidase preparations evaluated for the treatment of Pompe disease
A J McVie-Wylie, K L Lee, H Qiu, et al.
American Journal of Human Genetics
|
June 13, 1998
The African origin of the common mutation in African American patients with glycogen-storage disease type II
J A Becker, J Vlach, N Raben, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
The New England Journal of Medicine
|
August 10, 1995
Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene
J Walston, K Silver, C Bogardus, et al.
American Journal of Medical Genetics
|
September 17, 1998
Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease
F Martiniuk, A Chen, A Mack, et al.
Human Molecular Genetics
|
October 9, 2001
Conditional tissue-specific expression of the acid alpha-glucosidase (GAA) gene in the GAA knockout mice: implications for therapy
N Raben, N Lu, K Nagaraju, et al.
Neurology
|
June 27, 2001
Surprises of genetic engineering: a possible model of polyglucosan body disease
N Raben, M Danon, N Lu, et al.
Human Gene Therapy
|
March 27, 2001
Intercellular transfer of the virally derived precursor form of acid alpha-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy Pompe disease
D F Pauly, T J Fraites, C Toma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 2, 2000
Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies
K Nagaraju, N Raben, L Loeffler, et al.
Diabetes/Metabolism Research and Reviews
|
October 12, 2000
Molecular scanning for mutations in the insulin receptor substrate-1 (IRS-1) gene in Mexican Americans with Type 2 diabetes mellitus
F S Celi, C Negri, K Tanner, et al.
Molecular Genetics and Metabolism
|
June 10, 2008
Biochemical and pharmacological characterization of different recombinant acid alpha-glucosidase preparations evaluated for the treatment of Pompe disease
A J McVie-Wylie, K L Lee, H Qiu, et al.
American Journal of Human Genetics
|
June 13, 1998
The African origin of the common mutation in African American patients with glycogen-storage disease type II
J A Becker, J Vlach, N Raben, et al.
Page
of 5