Chromosomal deletions (deficiencies\u27) are powerful tools in the genetic analysis of complex genomes. They have been exploited extensively in Drosophila melanogaster, an organism in which deficiencies can be efficiently induced and selected. Spontaneous deletions in humans have facilitated the dissection of phenotypes in contiguous gene syndromes and led to the positional cloning of critical genes. In mice, deletion complexes created by whole animal irradiation experiments have enabled a systematic characterization of functional units along defined chromosomal regions. However, classical mutagenesis in mice is logistically impractical for generating deletion sets on a genome-wide scale. Here, we report a high-throughput method f...
Gene targeting in mouse embryonic stem (ES) cells can be used to generate single gene mutations or d...
The discovery of chromosomal translocations in leukemia/lymphoma and sarcomas presaged a widespread ...
SummaryStructural variations (SVs) contribute to the variability of our genome and are often associa...
As the genetic and physical mapping stage of the Human Genome Project nears completion, the focus is...
Chromosome deletions have several applications in the genetic analysis of complex organisms. They ca...
Chromosome deletion complexes in model organisms serve as valuable genetic tools for the functional ...
Chromosomal rearrangements have been instrumental in genetic studies in Drosophila. Visibly marked d...
CHROMOSOMAL rearrangements are the major cause of inherited human disease and fetal loss 1 . Transla...
Until the end of the 20th century, mouse germ cell data on induced mutation rates, which were collec...
<div><p>(A) Insertion of a negative selectable marker (cassette Neo-tk: Hsv-thymidine kinase/neomyci...
Experimental approaches for deciphering the function of human genes rely heavily on our ability to g...
Deletions, duplications, and inversions of large genomic regions covering several genes are an impor...
This article has been adapted, with permission, from a paper originally published in Médecine/ Scien...
Structural variations (SVs) contribute to the variability of our genome and are often associated wit...
Molecular biologists have elucidated general principles about chromosomal translocations by cloning ...
Gene targeting in mouse embryonic stem (ES) cells can be used to generate single gene mutations or d...
The discovery of chromosomal translocations in leukemia/lymphoma and sarcomas presaged a widespread ...
SummaryStructural variations (SVs) contribute to the variability of our genome and are often associa...
As the genetic and physical mapping stage of the Human Genome Project nears completion, the focus is...
Chromosome deletions have several applications in the genetic analysis of complex organisms. They ca...
Chromosome deletion complexes in model organisms serve as valuable genetic tools for the functional ...
Chromosomal rearrangements have been instrumental in genetic studies in Drosophila. Visibly marked d...
CHROMOSOMAL rearrangements are the major cause of inherited human disease and fetal loss 1 . Transla...
Until the end of the 20th century, mouse germ cell data on induced mutation rates, which were collec...
<div><p>(A) Insertion of a negative selectable marker (cassette Neo-tk: Hsv-thymidine kinase/neomyci...
Experimental approaches for deciphering the function of human genes rely heavily on our ability to g...
Deletions, duplications, and inversions of large genomic regions covering several genes are an impor...
This article has been adapted, with permission, from a paper originally published in Médecine/ Scien...
Structural variations (SVs) contribute to the variability of our genome and are often associated wit...
Molecular biologists have elucidated general principles about chromosomal translocations by cloning ...
Gene targeting in mouse embryonic stem (ES) cells can be used to generate single gene mutations or d...
The discovery of chromosomal translocations in leukemia/lymphoma and sarcomas presaged a widespread ...
SummaryStructural variations (SVs) contribute to the variability of our genome and are often associa...