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Scholar Results 1 - 7 of 7 citing Martin: Exendin-4 improves glycemic control, ameliorates brain and pancreatic pathologies,.... (0.12 sec) 

Huntington's Disease-New Perspectives Based on Neuroendocrine Changes in Rodent …


Å Petersén, S Hult, D Kirik - Neurodegenerative Dis, 2009 - content.karger.com
Huntington's disease (HD) is a neurodegenerative disorder caused by an expanded
CAG repeat in the huntingtin gene. Although it is characterized by progressive
motor impairments, cognitive changes and psychiatric disturbances are major ...
Cited by 1 - Related articles - All 3 versions

Emerging cardiovascular actions of the incretin hormone glucagon-like peptide-1: potential …


DJ Grieve, RS Cassidy, BD Green - British Journal of Pharmacology, 2009 - interscience.wiley.com
Glucagon-like peptide-1 (GLP-1) is an incretin hormone secreted by the small
intestine in response to nutrient ingestion. It has wide-ranging effects on
glucose metabolism, including stimulation of insulin release, inhibition of ...
Cited by 1 - Related articles - All 3 versions

Adenosine, Ketogenic Diet and Epilepsy: The Emerging Therapeutic Relationship Between …


SA Masino, M Kawamura Jr, CA Wasser, LT … - Current Neuropharmacology, 2009 - ingentaconnect.com
Abstract: For many years the neuromodulator adenosine has been recognized as an
endogenous anticonvulsant molecule and termed a “retaliatory metabolite.” As
the core molecule of ATP, adenosine forms a unique link between cell energy ...
Related articles

Beyond the brain: widespread pathology in Huntington's disease


JMM van der Burg, M Björkqvist, P Brundin - Lancet Neurology, 2009 - Elsevier
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by a
polyglutamine stretch in the huntingtin protein. Today, more than 15 years after
the genetic defect underlying HD was discovered, the pathogenesis is still ...
Related articles - All 11 versions

[PDF] Jorien MM van der Burg, Maria Björkqvist, Patrik Brundin


NS Unit, N Center, S Lund - Lancet Neurol, 2009 - med.lu.se
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by a
polyglutamine stretch in the huntingtin protein. Today, more than 15 years after
the genetic defect underlying HD was discovered, the pathogenesis is still ...
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Allosteric modulators of G protein-coupled receptors: Future therapeutics for complex …


L Wang, B Martin, R Brenneman, LM Luttrell, … - Journal of Pharmacology and Experimental …, 2009 - ASPET
G protein-coupled receptors (GPCRs) are one of the most important classes of
proteins in the genome, not only because of their tremendous molecular diversity
but because they are the targets of nearly 50% of current ...
Related articles - All 3 versions

Increased numbers of motor activity peaks during light cycle are associated with reductions …


FJ Bode, M Stephan, S Wiehager, HP Nguyen, M … - Behavioural Brain Research, 2009 - Elsevier
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG repeat
expansion in the HD gene. Besides psychiatric, motor and cognitive symptoms, HD
patients suffer from sleep disturbances. In order to screen a rat model ...
Related articles - All 2 versions


 


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