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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 Journal of Clinical Investigation
|
August 8, 2001
Loss of p27(Kip1) enhances the transplantation efficiency of hepatocytes transferred into diseased livers
A N Karnezis, M Dorokhov, M Grompe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 13, 2001
Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C
M Noll, R L Bateman, A D D'Andrea, et al.
Human Mutation
|
March 27, 1999
Identification of the mutation in the alkaptonuria mouse model. Mutations in brief no. 216. Online
K Manning, J M Fernández-Cañón, X Montagutelli, et al.
American Journal of Human Genetics
|
March 1, 1992
Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis
E Basler, M Grompe, G Parenti, et al.
Human Gene Therapy
|
February 1, 1992
Retroviral-mediated gene transfer of human ornithine transcarbamylase into primary hepatocytes of spf and spf-ash mice
M Grompe, S N Jones, H Loulseged, et al.
Human Genetics
|
May 1, 1992
Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR
M W Kilimann, A Pizzuti, M Grompe, et al.
Blood
|
January 11, 2000
Phenotypic correction of Fanconi anemia group C knockout mice
K A Gush, K L Fu, M Grompe, et al.
Molecular Biology & Medicine
|
December 1, 1989
Detection of new mutation disease in man and mouse
M Grompe, R A Gibbs, J S Chamberlain, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 78) with videos related to
Sort By:
Page
of 8
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 Journal of Clinical Investigation
|
August 8, 2001
Loss of p27(Kip1) enhances the transplantation efficiency of hepatocytes transferred into diseased livers
A N Karnezis, M Dorokhov, M Grompe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 13, 2001
Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C
M Noll, R L Bateman, A D D'Andrea, et al.
Human Mutation
|
March 27, 1999
Identification of the mutation in the alkaptonuria mouse model. Mutations in brief no. 216. Online
K Manning, J M Fernández-Cañón, X Montagutelli, et al.
American Journal of Human Genetics
|
March 1, 1992
Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis
E Basler, M Grompe, G Parenti, et al.
Human Gene Therapy
|
February 1, 1992
Retroviral-mediated gene transfer of human ornithine transcarbamylase into primary hepatocytes of spf and spf-ash mice
M Grompe, S N Jones, H Loulseged, et al.
Human Genetics
|
May 1, 1992
Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR
M W Kilimann, A Pizzuti, M Grompe, et al.
Blood
|
January 11, 2000
Phenotypic correction of Fanconi anemia group C knockout mice
K A Gush, K L Fu, M Grompe, et al.
Molecular Biology & Medicine
|
December 1, 1989
Detection of new mutation disease in man and mouse
M Grompe, R A Gibbs, J S Chamberlain, et al.
Page
of 8