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Pascale Hince Selected Research

Symporters

9/2008HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.

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Pascale Hince Research Topics

Disease

2Corpus callosum agenesis neuronopathy
10/2017 - 09/2008
2Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
03/2015 - 08/2012
2Hereditary Sensory and Motor Neuropathy (Dejerine Sottas Disease)
03/2012 - 09/2008
1Autosomal Recessive Primary Microcephaly
04/2016
1Hyperalgesia
03/2016
1Congenital Pain Insensitivity
03/2016
1Neuralgia (Stump Neuralgia)
03/2016
1Pain (Aches)
03/2016
1Lethal congenital contracture syndrome 1
03/2015
1Motor Neuron Disease (Primary Lateral Sclerosis)
03/2015
1Lethal Arthrogryposis With Anterior Horn Cell Disease
03/2015
1Neurodegenerative Diseases (Neurodegenerative Disease)
03/2012
1Colorectal Neoplasms (Colorectal Cancer)
04/2010

Drug/Important Bio-Agent (IBA)

4Proteins (Proteins, Gene)FDA Link
04/2016 - 09/2008
3Potassium ChlorideFDA LinkGeneric
10/2017 - 09/2008
3K Cl- CotransportersIBA
10/2017 - 09/2008
1Aminobutyrates (Aminobutyric Acid)IBA
03/2016
1gamma-Aminobutyric Acid (GABA)IBA
03/2016
1Phosphotransferases (Kinase)IBA
03/2016
1Messenger RNA (mRNA)IBA
03/2015
1Nonsense Codon (Nonsense Mutation)IBA
08/2012
1Netrin-1IBA
04/2010
1Creatine Kinase (Creatine Phosphokinase)IBA
09/2008
1EnzymesIBA
09/2008
1SymportersIBA
09/2008
1Adenosine Triphosphate (ATP)IBA
09/2008