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Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
Nucleotide sequence and organization of the mouse adenine phosphoribosyltransferase gene: presence of a coding region common to animal and bacterial phosphoribosyltransferases that has a variable intron/exon arrangementM K Dush, J M Sikela, S A Khan, et al.Environmental and Molecular Mutagenesis|January 1, 1996
APRT: a versatile in vivo resident reporter of local mutation and loss of heterozygosityP J Stambrook, C Shao, M Stockelman, et al.Journal of Cellular Biochemistry|March 1, 1997
Localization of group IIc low molecular weight phospholipase A2 mRNA to meiotic cells in the mouseJ Chen, C Shao, V Lazar, et al.Experimental Hematology|July 31, 1999
Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse modelR Bolante-Cervantes, S Li, A Sahota, et al.The Clinical Investigator|July 1, 1994
Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasisS Bye, R Mallmann, J Duley, et al.Gene|May 1, 1983
Cloning and expression of a mouse adenine phosphoribosyltransferase geneJ M Sikela, S A Khan, E Feliciano, et al.The Journal of Biological Chemistry|June 11, 1998
The functions of five distinct mammalian phospholipase A2S in regulating arachidonic acid release. Type IIa and type V secretory phospholipase A2S are functionally redundant and act in concert with cytosolic phospholipase A2M Murakami, S Shimbara, T Kambe, et al.American Journal of Human Genetics|May 1, 1991
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locusA Sahota, J Chen, M A Behzadian, et al.Cancer Research|July 26, 2000
Biallelic methylation and silencing of mouse Aprt in normal kidney cellsJ A Rose, P A Yates, J Simpson, et al.Mutation Research|June 1, 1993
Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: mutational hot spots at the intron 4 splice donor site and at codon 87J Chen, A Sahota, G F Martin, et al.Pageof 9