Two genes, HEXA and HEXB, encode the alpha- and beta-subunits, respectively, of human beta-hexosaminidase. In the mouse,...
...hexB, has also been proven to be related to the DNA mismatch repair system. As the first step to understand whether huma...
...HEXB genes, respectively. Extensive homology in both the gene structures and deduced primary sequences demonstrate their...
...HEXB promoter. Analysis of the tissue distribution of the HEXB mRNA in 129/Sv male mice revealed up to 28-fold tissue-sp...
...HexB) and S. cerevisiae yeast (PMS1). Disruption of the MLH1 gene results in elevated spontaneous mutation rates during ...
...HEXB and HTR1A) and two by polymerase chain reaction (PCR) amplification (HRH1 and ETH1112). These loci were assigned to...
Sandhoff disease is an autosomal recessive lysosomal storage disease resulting from mutations of the HEXB gene encoding ...
...HEXB gene encoding the beta subunit of the beta-hexosaminidases. In the present report, we examined the brain and liver ...
...HEXB, VIM, and APOB) for restriction fragment length polymorphisms (RFLP). A total of 14 polymorphisms, at least one at ...
...HEXB gene. Defects in the beta subunit lead to Sandhoff disease. Patients with the defect lack the activity or formation...
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