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M Grompe

Showing results (61-70 of 78) with videos related to

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Nature Genetics|August 1, 1995
Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type IM Grompe, S Lindstedt, M al-Dhalimy, et al.
Nature Medicine|November 4, 2000
Purified hematopoietic stem cells can differentiate into hepatocytes in vivoE Lagasse, H Connors, M Al-Dhalimy, et al.
American Journal of Medical Genetics|January 15, 1994
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterizationE A Lindsay, A Grillo, G B Ferrero, et al.
Molecular Cell|March 10, 2001
Positional cloning of a novel Fanconi anemia gene, FANCD2C Timmers, T Taniguchi, J Hejna, et al.
Genomics|September 1, 1995
Cloning and characterization of a human cDNA (INPPL1) sharing homology with inositol polyphosphate phosphatasesJ A Hejna, H Saito, L S Merkens, et al.
Molecular Genetics and Metabolism|March 13, 2001
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analysesB M Hogema, S Akaboshi, M Taylor, et al.
Molecular Medicine (Cambridge, Mass.)|August 26, 1998
Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transferM Pulsipher, G M Kupfer, D Naf, et al.
Diabetologia|September 2, 2011
Transcriptomes of the major human pancreatic cell typesC Dorrell, J Schug, C F Lin, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
Nature Genetics|September 7, 2001
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenaseB M Hogema, M Gupta, H Senephansiri, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Nature Genetics|August 1, 1995
Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type IM Grompe, S Lindstedt, M al-Dhalimy, et al.
Nature Medicine|November 4, 2000
Purified hematopoietic stem cells can differentiate into hepatocytes in vivoE Lagasse, H Connors, M Al-Dhalimy, et al.
American Journal of Medical Genetics|January 15, 1994
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterizationE A Lindsay, A Grillo, G B Ferrero, et al.
Molecular Cell|March 10, 2001
Positional cloning of a novel Fanconi anemia gene, FANCD2C Timmers, T Taniguchi, J Hejna, et al.
Genomics|September 1, 1995
Cloning and characterization of a human cDNA (INPPL1) sharing homology with inositol polyphosphate phosphatasesJ A Hejna, H Saito, L S Merkens, et al.
Molecular Genetics and Metabolism|March 13, 2001
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analysesB M Hogema, S Akaboshi, M Taylor, et al.
Molecular Medicine (Cambridge, Mass.)|August 26, 1998
Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transferM Pulsipher, G M Kupfer, D Naf, et al.
Diabetologia|September 2, 2011
Transcriptomes of the major human pancreatic cell typesC Dorrell, J Schug, C F Lin, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
Nature Genetics|September 7, 2001
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenaseB M Hogema, M Gupta, H Senephansiri, et al.
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