4.5 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

Related references

Note: Only part of the references are listed.
Article Neurosciences

Selective degeneration in YAC mouse models of Huntington disease

Jeremy M. Van Raamsdonk et al.

BRAIN RESEARCH BULLETIN (2007)

Article Biochemistry & Molecular Biology

Mitochondrial dysfunction in Huntington's disease:: the bioenergetics of isolated and in situ mitochondria from transgenic mice

Jorge M. A. Oliveira et al.

JOURNAL OF NEUROCHEMISTRY (2007)

Article Cell & Tissue Engineering

Huntington's disease: Pathological mechanisms and therapeutic strategies

Shilpa Ramaswamy et al.

CELL TRANSPLANTATION (2007)

Article Biochemistry & Molecular Biology

Inhibition of 26S proteasome activity by huntingtin filaments but not inclusion bodies isolated from mouse and human brain

Miguel Diaz-Hernandez et al.

JOURNAL OF NEUROCHEMISTRY (2006)

Article Biochemistry & Molecular Biology

Dopamine release is severely compromised in the R6/2 mouse model of Huntington's disease

MA Johnson et al.

JOURNAL OF NEUROCHEMISTRY (2006)

Article Neurosciences

Reduced expression of the TrkB receptor in Huntington's disease mouse models and in human brain

S Ginés et al.

EUROPEAN JOURNAL OF NEUROSCIENCE (2006)

Article Clinical Neurology

Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice

ZZ Gizatullina et al.

ANNALS OF NEUROLOGY (2006)

Article Biochemistry & Molecular Biology

Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease

JM Van Raamsdonk et al.

HUMAN MOLECULAR GENETICS (2005)

Article Biochemistry & Molecular Biology

Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant Huntingtin

T Milakovic et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Pharmacology & Pharmacy

Progressive loss of BDNF in a mouse model of Huntington's disease and rescue by BDNF delivery

C Zuccato et al.

PHARMACOLOGICAL RESEARCH (2005)

Article Biochemistry & Molecular Biology

Brain-derived neurotrophic factor modulates dopaminergic deficits in a transgenic mouse model of Huntington's disease

JR Pineda et al.

JOURNAL OF NEUROCHEMISTRY (2005)

Article Clinical Neurology

Generalized brain and skin proteasome inhibition in Huntington's disease

H Seo et al.

ANNALS OF NEUROLOGY (2004)

Article Biochemistry & Molecular Biology

Accumulation of aberrant ubiquitin induces aggregate formation and cell death in polyglutamine diseases

R de Pril et al.

HUMAN MOLECULAR GENETICS (2004)

Article Medicine, General & Internal

Mechanism of neurodegenerative disease: role of the ubiquitin proteasome system

L Petrucelli et al.

ANNALS OF MEDICINE (2004)

Article Neurosciences

NMDA receptor function in mouse models of Huntington disease

C Cepeda et al.

JOURNAL OF NEUROSCIENCE RESEARCH (2001)

Article Multidisciplinary Sciences

Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease

C Zuccato et al.

SCIENCE (2001)