Indraccolo, S <br/><br/>
Mutator phenotype in human hematopoietic neoplasms and its association with deletions disabling DNA repair genes and bcl-2 rearrangements.  [electronic resource] 

 -  Blood  Oct 1999 
 - 2424-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Adenosine Triphosphatases<br/>Adult<br/>Aged<br/>Animals<br/>Carrier Proteins<br/>Cell Survival<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3<br/>Chromosomes, Human, Pair 7<br/>DNA Repair--genetics<br/>DNA Repair Enzymes<br/>DNA-Binding Proteins<br/>Female<br/>Gene Rearrangement<br/>Genes, bcl-2<br/>Humans<br/>Loss of Heterozygosity<br/>Lymphoma, Non-Hodgkin--genetics<br/>Male<br/>Mice<br/>Microsatellite Repeats<br/>Middle Aged<br/>Mismatch Repair Endonuclease PMS2<br/>MutL Protein Homolog 1<br/>MutS Homolog 2 Protein<br/>Neoplasm Proteins--genetics<br/>Nuclear Proteins<br/>Phenotype<br/>Precursor Cell Lymphoblastic Leukemia-Lymphoma--genetics<br/>Proteins--genetics<br/>Proto-Oncogene Mas<br/>Proto-Oncogene Proteins--genetics<br/>Sequence Deletion