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American Journal of Human Genetics
|
October 1, 1992
Gaucher disease: A G+1----A+1 IVS2 splice donor site mutation causing exon 2 skipping in the acid beta-glucosidase mRNA
G S He, G A Grabowski
American Journal of Human Genetics
|
May 1, 1989
Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts
J E Bergmann, G A Grabowski
Methods in Cell Biology
|
January 1, 1982
Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospects
G A Grabowski, R J Desnick
The Journal of Biological Chemistry
|
November 17, 1995
Characterization of lysosomal acid lipase by site-directed mutagenesis and heterologous expression
S Sheriff, H Du, G A Grabowski
DNA and Cell Biology
|
March 7, 2002
In vivo roles of RORalpha and Sp4 in the regulation of murine prosaposin gene
P Jin, Y Sun, G A Grabowski
The Journal of Biological Chemistry
|
June 17, 1994
Functional human saposins expressed in Escherichia coli. Evidence for binding and activation properties of saposins C with acid beta-glucosidase
X Qi, T Leonova, G A Grabowski
Blood Reviews
|
July 14, 1998
Enzyme therapy for Gaucher disease: the first 5 years
G A Grabowski, N Leslie, R Wenstrup
DNA and Cell Biology
|
January 1, 1997
The mouse prosaposin locus: promoter organization
Y Sun, P Jin, G A Grabowski
Critical Reviews in Biochemistry and Molecular Biology
|
January 1, 1990
Acid beta-glucosidase: enzymology and molecular biology of Gaucher disease
G A Grabowski, S Gatt, M Horowitz
The Journal of Biological Chemistry
|
May 28, 1998
Role of Sp proteins and RORalpha in transcription regulation of murine prosaposin
P Jin, Y Sun, G A Grabowski
Page
of 13
Search research articles
Search
Showing results (21-30 of 126) with videos related to
Sort By:
Page
of 13
American Journal of Human Genetics
|
October 1, 1992
Gaucher disease: A G+1----A+1 IVS2 splice donor site mutation causing exon 2 skipping in the acid beta-glucosidase mRNA
G S He, G A Grabowski
American Journal of Human Genetics
|
May 1, 1989
Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts
J E Bergmann, G A Grabowski
Methods in Cell Biology
|
January 1, 1982
Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospects
G A Grabowski, R J Desnick
The Journal of Biological Chemistry
|
November 17, 1995
Characterization of lysosomal acid lipase by site-directed mutagenesis and heterologous expression
S Sheriff, H Du, G A Grabowski
DNA and Cell Biology
|
March 7, 2002
In vivo roles of RORalpha and Sp4 in the regulation of murine prosaposin gene
P Jin, Y Sun, G A Grabowski
The Journal of Biological Chemistry
|
June 17, 1994
Functional human saposins expressed in Escherichia coli. Evidence for binding and activation properties of saposins C with acid beta-glucosidase
X Qi, T Leonova, G A Grabowski
Blood Reviews
|
July 14, 1998
Enzyme therapy for Gaucher disease: the first 5 years
G A Grabowski, N Leslie, R Wenstrup
DNA and Cell Biology
|
January 1, 1997
The mouse prosaposin locus: promoter organization
Y Sun, P Jin, G A Grabowski
Critical Reviews in Biochemistry and Molecular Biology
|
January 1, 1990
Acid beta-glucosidase: enzymology and molecular biology of Gaucher disease
G A Grabowski, S Gatt, M Horowitz
The Journal of Biological Chemistry
|
May 28, 1998
Role of Sp proteins and RORalpha in transcription regulation of murine prosaposin
P Jin, Y Sun, G A Grabowski
Page
of 13