Found: 17
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Generation and characterization of a knock-in mouse model for spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM).
- Published in:
- Mammalian Genome, 2023, v. 34, n. 4, p. 572, doi. 10.1007/s00335-023-10013-4
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- Article
35th International Mammalian Genome Conference: meeting overview.
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- Mammalian Genome, 2023, v. 34, n. 3, p. 449, doi. 10.1007/s00335-023-09983-2
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- Article
Chronic and age-dependent effects of the spongiform neurodegeneration-associated MGRN1 E3 ubiquitin ligase on mitochondrial homeostasis.
- Published in:
- Mammalian Genome, 2019, v. 30, n. 5/6, p. 151, doi. 10.1007/s00335-019-09802-7
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- Article
Meeting report: 31st International Mammalian Genome Conference, Mammalian Genetics and Genomics: From Molecular Mechanisms to Translational Applications.
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- Mammalian Genome, 2018, v. 29, n. 5/6, p. 299, doi. 10.1007/s00335-018-9747-6
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- Article
Accessory Proteins for Melanocortin Signaling.
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- Annals of the New York Academy of Sciences, 2003, v. 994, n. 1, p. 288, doi. 10.1111/j.1749-6632.2003.tb03192.x
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- Article
Levels of the Mahogunin Ring Finger 1 E3 Ubiquitin Ligase Do Not Influence Prion Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055575
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- Article
A biochemical function for attractin in agouti-induced pigmentation and obesity.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 40, doi. 10.1038/83741
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- Article
Molecular Pharmacology of Agouti Protein in Vitro and in Vivo.
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- Annals of the New York Academy of Sciences, 1999, v. 885, n. 1, p. 143, doi. 10.1111/j.1749-6632.1999.tb08671.x
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- Article
The mouse mahogany locus encodes a transmembrane form of human attraction.
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- Nature, 1999, v. 398, n. 6723, p. 152, doi. 10.1038/18217
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- Article
Mice with mutations in Mahogunin ring finger-1 ( Mgrn1) exhibit abnormal patterning of the left-right axis.
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- Developmental Dynamics, 2006, v. 235, n. 12, p. 3438, doi. 10.1002/dvdy.20992
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- Article
MGRN1-dependent pigment-type switching requires its ubiquitination activity but not its interaction with TSG101 or NEDD4.
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- Pigment Cell & Melanoma Research, 2013, v. 26, n. 2, p. 263, doi. 10.1111/pcmr.12059
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- Article
Greg Barsh.
- Published in:
- 2011
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- Publication type:
- Other
Shades of meaning: the pigment-type switching system as a tool for discovery.
- Published in:
- Pigment Cell & Melanoma Research, 2010, v. 23, n. 4, p. 485, doi. 10.1111/j.1755-148X.2010.00721.x
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- Article
Piecing together the pigment-type switching puzzle.
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- Pigment Cell & Melanoma Research, 2010, v. 23, n. 1, p. 4, doi. 10.1111/j.1755-148X.2009.00654.x
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- Article
Oligodendroglial deletion of ESCRT-I component TSG101 causes spongiform encephalopathy.
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- Biology of the Cell (Wiley-Blackwell), 2016, v. 108, n. 11, p. 324, doi. 10.1111/boc.201600014
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- Article
Identification and preliminary characterization of mouse Adam33.
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- BMC Genetics, 2002, v. 3, p. 1
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- Article
Functional annotation and ENU.
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- BMC Research Notes, 2012, v. 5, n. 1, p. 1, doi. 10.1186/1756-0500-5-580
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- Article