Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 261, doi. 10.1007/s00335-011-9321-y
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- Publication type:
- Article
Works matching IS 09388990 AND DT 2011 AND VI 22 AND IP 5/6
Results: 9
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Decreased expression of Flightless I, a gelsolin family member and developmental regulator, in early-gestation fetal wounds improves healing.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 341, doi. 10.1007/s00335-011-9320-z
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- Article
3
Intersubspecific subcongenic mouse strain analysis reveals closely linked QTLs with opposite effects on body weight.
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- Mammalian Genome, 2011, v. 22, n. 5/6, p. 282, doi. 10.1007/s00335-011-9323-9
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- Publication type:
- Article
4
Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 353, doi. 10.1007/s00335-011-9325-7
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- Publication type:
- Article
5
A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 290, doi. 10.1007/s00335-011-9324-8
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- Publication type:
- Article
6
Functional PAK-2 knockout and replacement with a caspase cleavage-deficient mutant in mice reveals differential requirements of full-length PAK-2 and caspase-activated PAK-2p34.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 306, doi. 10.1007/s00335-011-9326-6
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- Publication type:
- Article
7
Uncovering the transcriptional circuitry in skeletal muscle regeneration.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 272, doi. 10.1007/s00335-011-9322-x
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- Publication type:
- Article
8
The influence of sex and estrous cycle on QTL for emotionality and ethanol consumption.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 329, doi. 10.1007/s00335-011-9327-5
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- Publication type:
- Article
9
ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type.
- Published in:
- Mammalian Genome, 2011, v. 22, n. 5/6, p. 318, doi. 10.1007/s00335-011-9329-3
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- Publication type:
- Article