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79 in total

1. Use of a small palindrome genetic marker to investigate mechanisms of double-strand-break repair in mammalian cells.

Authors: J Li; M D Baker
Journal: Genetics Date: 2000-03 Impact factor: 4.562

2. Spontaneous loss of heterozygosity in diploid Saccharomyces cerevisiae cells.

Authors: M Hiraoka; K Watanabe; K Umezu; H Maki
Journal: Genetics Date: 2000-12 Impact factor: 4.562

3. Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells.

Authors: R D Johnson; M Jasin
Journal: EMBO J Date: 2000-07-03 Impact factor: 11.598

4. Loss of heterozygosity analysis using whole genome amplification, cell sorting, and fluorescence-based PCR.

Authors: T G Paulson; P C Galipeau; B J Reid
Journal: Genome Res Date: 1999-05 Impact factor: 9.043

5. Basic research on the biology of meta-tetra(hydroxyphenyl) chlorin for photodynamic therapy in gynaecology: Somatic genotoxicity assayed withDrosophila melanogaster.

Authors: P M Schweizer; H Walt; M Fehr; U Haller
Journal: Lasers Med Sci Date: 1997-10 Impact factor: 3.161

6. Simultaneous assessment of loss of heterozygosity at multiple microsatellite loci using semi-automated fluorescence-based detection: subregional mapping of chromosome 4 in cervical carcinoma.

Authors: G M Hampton; A A Larson; R N Baergen; R L Sommers; S Kern; W K Cavenee
Journal: Proc Natl Acad Sci U S A Date: 1996-06-25 Impact factor: 11.205

7. Loss of heterozygosity induced by a chromosomal double-strand break.

Authors: M E Moynahan; M Jasin
Journal: Proc Natl Acad Sci U S A Date: 1997-08-19 Impact factor: 11.205

8. Structural analysis of aberrant chromosomes that occur spontaneously in diploid Saccharomyces cerevisiae: retrotransposon Ty1 plays a crucial role in chromosomal rearrangements.

Authors: Keiko Umezu; Mina Hiraoka; Masaaki Mori; Hisaji Maki
Journal: Genetics Date: 2002-01 Impact factor: 4.562

9. Codon 249 mutations of p53 gene in development of hepatocellular carcinoma.

Authors: Xiao-Mou Peng; Wen-Wei Peng; Ji-Lu Yao
Journal: World J Gastroenterol Date: 1998-04 Impact factor: 5.742

10. Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors: A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal: Hum Mol Genet Date: 1993-02 Impact factor: 6.150