CHIP and HSPs interact with β-APP in a proteasome-dependent manner and influence Aβ metabolism.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 848, doi. 10.1093/hmg/ddm030
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 7
Results: 12
1
2
Assessment and disease comparisons of hybrid developmental defects.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 808, doi. 10.1093/hmg/ddm025
- By:
- Publication type:
- Article
3
Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 837, doi. 10.1093/hmg/ddm029
- By:
- Publication type:
- Article
4
Translational control of SEPT9 isoforms is perturbed in disease.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 742, doi. 10.1093/hmg/ddm003
- By:
- Publication type:
- Article
5
Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 753, doi. 10.1093/hmg/ddm006
- By:
- Publication type:
- Article
6
Pleiotropic impact of constitutive fosB inactivation on nicotine-induced behavioral alterations and stress-related traits in mice.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 820, doi. 10.1093/hmg/ddm027
- By:
- Publication type:
- Article
7
Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 798, doi. 10.1093/hmg/ddm024
- By:
- Publication type:
- Article
8
A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1–Cog8 interaction in COG complex formation.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 717, doi. 10.1093/hmg/ddl476
- By:
- Publication type:
- Article
9
Extended polyglutamine repeats trigger a feedback loop involving the mitochondrial complex III, the proteasome and huntingtin aggregates.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 783, doi. 10.1093/hmg/ddm023
- By:
- Publication type:
- Article
10
COG8 deficiency causes new congenital disorder of glycosylation type IIh.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 731, doi. 10.1093/hmg/ddm028
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- Publication type:
- Article
11
Trisomy for the Down syndrome ‘critical region’ is necessary but not sufficient for brain phenotypes of trisomic mice.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 774, doi. 10.1093/hmg/ddm022
- By:
- Publication type:
- Article
12
Success and failure in human spermatogenesis as revealed by teratozoospermic RNAs.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 763, doi. 10.1093/hmg/ddm012
- By:
- Publication type:
- Article