- Abstract:
-
International efforts to test gene function in the mouse by the systematic knockout of each gene are creating many lines in which embryonic development is compromised. These homozygous lethal mutants represent a potential treasure trove for the biomedical community. Developmental biologists could exploit them in their studies of tissue differentiation and organogenesis; for clinical researchers they offer a powerful resource for investigating the origins of developmental diseases that affect ...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1242/dmm.011957
-
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- Journal:
- Disease models and mechanisms
- Volume:
- 6
- Issue:
- 3
- Pages:
- 562-566
- Publication date:
- 2013-05-05
- DOI:
- EISSN:
-
1754-8411
- ISSN:
-
1754-8403
- URN:
-
uuid:f8bfc6f8-7bc5-4c31-a3ad-b63418964d41
- Source identifiers:
-
405759
- Local pid:
- pubs:405759
- Language:
- English
- Keywords:
- Copyright date:
- 2013
Journal article
Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice.
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