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Human Mutation
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January 1, 1993
Mutations of the fumarylacetoacetate hydrolase gene in four patients with tyrosinemia, type I
M Grompe, M al-Dhalimy
Biochemical Medicine and Metabolic Biology
|
August 1, 1992
Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase
M Grompe, M al-Dhalimy
Molecular Genetics and Metabolism
|
February 5, 2002
Long-term therapy with NTBC and tyrosine-restricted diet in a murine model of hereditary tyrosinemia type I
M Al-Dhalimy, K Overturf, M Finegold, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 16, 1999
In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I
K Manning, M Al-Dhalimy, M Finegold, et al.
Journal of Inherited Metabolic Disease
|
September 5, 1998
Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report
M Grompe, K Overturf, M al-Dhalimy, et al.
The American Journal of Pathology
|
December 14, 1999
The repopulation potential of hepatocyte populations differing in size and prior mitotic expansion
K Overturf, M Al-Dhalimy, M Finegold, et al.
The American Journal of Pathology
|
February 13, 2001
Liver repopulation and correction of metabolic liver disease by transplanted adult mouse pancreatic cells
X Wang, M Al-Dhalimy, E Lagasse, et al.
The American Journal of Pathology
|
November 14, 1997
Serial transplantation reveals the stem-cell-like regenerative potential of adult mouse hepatocytes
K Overturf, M al-Dhalimy, C N Ou, et al.
Human Gene Therapy
|
March 21, 1998
Ex vivo hepatic gene therapy of a mouse model of Hereditary Tyrosinemia Type I
K Overturf, M Al-Dhalimy, K Manning, et al.
The New England Journal of Medicine
|
August 11, 1994
A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I
M Grompe, M St-Louis, S I Demers, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Human Mutation
|
January 1, 1993
Mutations of the fumarylacetoacetate hydrolase gene in four patients with tyrosinemia, type I
M Grompe, M al-Dhalimy
Biochemical Medicine and Metabolic Biology
|
August 1, 1992
Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase
M Grompe, M al-Dhalimy
Molecular Genetics and Metabolism
|
February 5, 2002
Long-term therapy with NTBC and tyrosine-restricted diet in a murine model of hereditary tyrosinemia type I
M Al-Dhalimy, K Overturf, M Finegold, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 16, 1999
In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I
K Manning, M Al-Dhalimy, M Finegold, et al.
Journal of Inherited Metabolic Disease
|
September 5, 1998
Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report
M Grompe, K Overturf, M al-Dhalimy, et al.
The American Journal of Pathology
|
December 14, 1999
The repopulation potential of hepatocyte populations differing in size and prior mitotic expansion
K Overturf, M Al-Dhalimy, M Finegold, et al.
The American Journal of Pathology
|
February 13, 2001
Liver repopulation and correction of metabolic liver disease by transplanted adult mouse pancreatic cells
X Wang, M Al-Dhalimy, E Lagasse, et al.
The American Journal of Pathology
|
November 14, 1997
Serial transplantation reveals the stem-cell-like regenerative potential of adult mouse hepatocytes
K Overturf, M al-Dhalimy, C N Ou, et al.
Human Gene Therapy
|
March 21, 1998
Ex vivo hepatic gene therapy of a mouse model of Hereditary Tyrosinemia Type I
K Overturf, M Al-Dhalimy, K Manning, et al.
The New England Journal of Medicine
|
August 11, 1994
A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I
M Grompe, M St-Louis, S I Demers, et al.
Page
of 2