Murine albino-deletion complex: High-resolution microsatellite map and genetically...
- Published in:
- Genetics, 1997, v. 147, n. 2, p. 787, doi. 10.1093/genetics/147.2.787
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- Publication type:
- Article
Works by Johnson, Dabney K.
Results: 11
1
2
Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus.
- Published in:
- Genetics, 1995, v. 141, n. 4, p. 1563, doi. 10.1093/genetics/141.4.1563
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- Publication type:
- Article
3
Cdc14B depletion leads to centriole amplification, and its overexpression prevents unscheduled centriole duplication.
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- Journal of Cell Biology, 2008, v. 181, n. 3, p. 475, doi. 10.1083/jcb.200710127
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- Publication type:
- Article
4
Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 8, p. 1329, doi. 10.1093/hmg/ddl053
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- Publication type:
- Article
5
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 3, p. 533
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- Publication type:
- Article
6
The Collaborative Cross at Oak Ridge National Laboratory: developing a powerful resource for systems genetics.
- Published in:
- Mammalian Genome, 2008, v. 19, n. 6, p. 382, doi. 10.1007/s00335-008-9135-8
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- Publication type:
- Article
7
Neurobehavioral mutants identified in an ENU-mutagenesis project.
- Published in:
- Mammalian Genome, 2007, v. 18, n. 8, p. 559, doi. 10.1007/s00335-007-9035-3
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- Publication type:
- Article
8
Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader–Willi syndrome mouse models.
- Published in:
- Mammalian Genome, 2005, v. 16, n. 6, p. 424, doi. 10.1007/s00335-005-2460-2
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- Publication type:
- Article
9
Identification of mutations from phenotype-driven ENU mutagenesis in mouse Chromosome 7.
- Published in:
- Mammalian Genome, 2005, v. 16, n. 8, p. 555, doi. 10.1007/s00335-005-0032-0
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- Publication type:
- Article
10
Cloning, functional study and comparative mapping of Luzp2 to mouse Chromosome 7 and human Chromosome 11p13–11p14.
- Published in:
- Mammalian Genome, 2003, v. 14, n. 5, p. 323, doi. 10.1007/s00335-002-2248-6
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- Publication type:
- Article
11
A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 1, p. 58, doi. 10.1007/s003350010011
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- Publication type:
- Article