Characterization and chromosomal mapping of a genomic clone encoding human alanine:Glyoxylate aminotransferase
- 31 May 1991
- Vol. 10 (1) , 34-42
- https://doi.org/10.1016/0888-7543(91)90481-s
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Molecular and Clinical Heterogeneity in Primary Hyperoxaluria Type 1American Journal of Kidney Diseases, 1991
- The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reactionGenomics, 1989
- An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.The Journal of cell biology, 1989
- Further studies on the activity and subcellular distribution of alanine: Glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1Clinical Science, 1988
- Interaction of a Liver-Specific Nuclear Factor with the Fibrinogen and α 1 -Antitrypsin PromotersScience, 1987
- Factors involved in control of tissue-specific expression of albumin geneCell, 1987
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986
- Assignment of the haemophilia B (Factor IX) locus to the q26‐qter region of the X chromosomeAnnals of Human Genetics, 1984
- Screening λgt Recombinant Clones by Hybridization to Single Plaques in SituScience, 1977
- SOMATIC CELL HYBRIDS BETWEEN MOUSE PERITONEAL MACROPHAGES AND SV40-TRANSFORMED HUMAN CELLSThe Journal of Experimental Medicine, 1974