Detection of Lis1 gene frame shift mutation in human hepatocarcinoma

Acta Biochimica et Biophysica Sinica

Volumn 32, Issue 4, 2000, Pages 404-405

  Xia, Shuang Luo ^a   Zhao, Mu Jun ^b   Wu, Zhen Yu ^b   Li, Zai Ping ^b  

^a SHANGHAI UNIVERSITY   (China)

^b INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

Author keywords

Frame shift mutation; GST fusion protein; Lis1 gene; PTT

Indexed keywords

EID: 20444380991     PISSN: 05829879     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Dunnen J T, Ommen G B. The protein truncation test: a review. Hum Mutation, 1999, 14: 95-102
2. Orly R et al. Isolation of a Miller-Dieker lissencehaply gene containing G protein β-subunit-like repeats. Nat Genet, 1993, 364: 717-721
3. Daniela T P et al. Lis1 and XLis (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet, 1998, 13: 2029-2037
4. Farrington S M, Lin G J, Ling J, Wang Y, Burczak J D, Dunlop M G. Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls. Am J Hum Genet, 1998, 63: 749-759
5. Ozcelik H et al. Germline BRCA 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients. Nat Genet, 1997, 16: 17-18