Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 20
Results: 19
Blocking acid-sensing ion channel 1 alleviates Huntington's disease pathology via an ubiquitin-proteasome system-dependent mechanism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3223, doi. 10.1093/hmg/ddn218
- By:
- Publication type:
- Article
Compensatory changes in the ubiquitin–proteasome system, brain-derived neurotrophic factor and mitochondrial complex II/III in YAC72 and R6/2 transgenic mice partially model Huntington's disease patients.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3144, doi. 10.1093/hmg/ddn211
- By:
- Publication type:
- Article
Failure of bone morphogenetic protein receptor trafficking in pulmonary arterial hypertension: potential for rescue.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3180, doi. 10.1093/hmg/ddn214
- By:
- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. NP, doi. 10.1093/hmg/ddn315
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. NP, doi. 10.1093/hmg/ddn314
- Publication type:
- Article
Neocortical expression of mutant huntingtin is not required for alterations in striatal gene expression or motor dysfunction in a transgenic mouse.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3095, doi. 10.1093/hmg/ddn206
- By:
- Publication type:
- Article
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3118, doi. 10.1093/hmg/ddn209
- By:
- Publication type:
- Article
Mice lacking the schizophrenia-associated protein FEZ1 manifest hyperactivity and enhanced responsiveness to psychostimulants.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3191, doi. 10.1093/hmg/ddn215
- By:
- Publication type:
- Article
Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3212, doi. 10.1093/hmg/ddn217
- By:
- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. NP, doi. 10.1093/hmg/ddn316
- Publication type:
- Article
Polycystin-2 down-regulates cell proliferation via promoting PERK-dependent phosphorylation of eIF2α.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3254, doi. 10.1093/hmg/ddn221
- By:
- Publication type:
- Article
Replication independent ATR signalling leads to G2/M arrest requiring Nbs1, 53BP1 and MDC1.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3247, doi. 10.1093/hmg/ddn220
- By:
- Publication type:
- Article
Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3154, doi. 10.1093/hmg/ddn212
- By:
- Publication type:
- Article
Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3204, doi. 10.1093/hmg/ddn216
- By:
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. NP, doi. 10.1093/hmg/ddn317
- Publication type:
- Article
Parkin deletion causes cerebral and systemic amyloidosis in human mutated tau over-expressing mice.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3128
- By:
- Publication type:
- Article
Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3236, doi. 10.1093/hmg/ddn219
- By:
- Publication type:
- Article
Polycystin-1 C-terminal tail associates with β-catenin and inhibits canonical Wnt signaling.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3105, doi. 10.1093/hmg/ddn208
- By:
- Publication type:
- Article
Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz–Jampel syndrome neuromyotonia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3166, doi. 10.1093/hmg/ddn213
- By:
- Publication type:
- Article