Pages that link to "Q21498879"
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The following pages link to Galactosidase, alpha (Q21498879):
Displaying 19 items.
- Gla (Q14886382) (← links)
- Fabry disease: preclinical studies demonstrate the effectiveness of alpha-galactosidase A replacement in enzyme-deficient mice (Q28345052) (← links)
- Local and global cerebral blood flow and glucose utilization in the alpha-galactosidase A knockout mouse model of Fabry disease (Q28506514) (← links)
- Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cells (Q28507358) (← links)
- Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation (Q28507844) (← links)
- X-linked inheritance of a structural gene for alpha-galactosidase in Mus musculus (Q28508108) (← links)
- X-linked and autosomal genes controlling mouse alpha-galactosidase expression (Q28508289) (← links)
- Gene mapping in Mus musculus by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2 (Q28509504) (← links)
- Infrared imaging microscopy of bone: illustrations from a mouse model of Fabry disease (Q28509709) (← links)
- Expression of alpha-galactosidase in preimplantation mouse embryos (Q28511003) (← links)
- Multilocus molecular mapping of the mouse X chromosome (Q28511704) (← links)
- Electrophoretic variation for X chromosome-linked hypoxanthine phosphoribosyl transferase (HPRT) in wild-derived mice. (Q28512016) (← links)
- Comparative gene mapping: order of loci on the X chromosome is different in mice and humans (Q28512604) (← links)
- alpha-Galactosidase A deficient mice: a model of Fabry disease (Q28513530) (← links)
- Mice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity (Q28584902) (← links)
- A synthetic chaperone corrects the trafficking defect and disease phenotype in a protein misfolding disorder (Q28586169) (← links)
- Alpha-galactosidase A deficiency accelerates atherosclerosis in mice with apolipoprotein E deficiency (Q28591035) (← links)
- Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome (Q28593513) (← links)
- Wikidata:Database reports/Constraint violations/P680 (← links | edit)