A. Neu

发表

Opposing modifications in intrinsic currents and synaptic inputs in post-traumatic mossy cells: evidence for single-cell homeostasis in a hyperexcitable network.

Julio C. Echegoyen, R. Morgan, I. Soltesz, 2007, Journal of neurophysiology.

Severe congenital contractural arachnodactyly caused by biallelic pathogenic variants in FBN2.

K. Kutsche, A. Volk, K. Kloth, 2021, European journal of medical genetics.

Differential regulation of AMPK activation in leptin‐and creatine‐deficient mice

D. Isbrandt, K. Sauter, C. Choe, 2013, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy.

M. Meisler, J. Denecke, M. Amling, 2017, Bone.

Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness.

L. T. ’t Hart, G. Janssen, A. Neu, 2006, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Cognitive performance of 20 healthy humans supplemented with L-homoarginine for 4 weeks

C. Gerloff, J. Hoppe, E. Schwedhelm, 2018, Journal of Clinical Neuroscience.

Creatine, guanidinoacetate and homoarginine in statin-induced myopathy

C. Gerloff, E. Schwedhelm, D. Isbrandt, 2020, Amino Acids.

Control of glial cell volume in anoxia. In vitro studies on ischemic cell swelling.

O. Kempski, A. Baethmann, A. Neu, 1987, Stroke.

The weaver Mouse gain-of-functionPhenotype of Dopaminergic Midbrain Neurons Is Determined by Coactivation of wvGirk2 and K-ATP Channels

B. Liss, J. Roeper, A. Neu, 1999, The Journal of Neuroscience.

Homoarginine supplementation improves blood glucose in diet-induced obese mice

E. Schwedhelm, D. Isbrandt, R. Böger, 2015, Amino Acids.

Guanidino compound ratios are associated with stroke etiology, internal carotid artery stenosis and CHA2DS2-VASc score in three cross-sectional studies

C. Gerloff, G. Thomalla, E. Schwedhelm, 2019, Journal of the Neurological Sciences.

Swelling Behavior of C6 Glioma Cells During Shutdown of Energy Metabolism

O. Kempski, A. Baethmann, A. Neu, 1986 .

Homoarginine supplementation improves blood glucose in diet-induced obese mice

E. Schwedhelm, D. Isbrandt, R. Böger, 2015, Amino Acids.

Transcriptomic and metabolic analyses reveal salvage pathways in creatine-deficient AGAT−/− mice

K. Kharbanda, D. Isbrandt, K. Sauter, 2016, Amino Acids.

Treatment during a vulnerable developmental period rescues a genetic epilepsy

Christophe Bernard, Dirk Isbrandt, Fabio Morellini, 2015, Nature Medicine.

de novo MEPCE nonsense variant associated with a neurodevelopmental disorder causes disintegration of 7SK snRNP and enhanced RNA polymerase II activation

K. Kutsche, M. Hempel, A. Neu, 2019, Scientific Reports.

Cell type–specific gating of perisomatic inhibition by cholecystokinin

I. Soltesz, J. Szabadics, Soo Yeun Lee, 2007, Nature Neuroscience.

Glutaric aciduria type I: Pathomechanisms of neurodegeneration

E. Christensen, C. Jakobs, T. Lücke, 1999, Journal of Inherited Metabolic Disease.

Ih Channels Contribute to the Different Functional Properties of Identified Dopaminergic Subpopulations in the Midbrain

Jochen Roeper, Axel Neu, Birgit Liss, 2002, The Journal of Neuroscience.

Single‐cell mRNA expression of HCN1 correlates with a fast gating phenotype of hyperpolarization‐activated cyclic nucleotide‐gated ion channels (Ih) in central neurons

B. Liss, J. Roeper, O. Franz, 2000, The European journal of neuroscience.

Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports

M. Synofzik, B. Wissinger, C. Kernstock, 2019, BMC Medical Genetics.

Epilepsy With Febrile Seizures Plus Sodium Channel Mutations That Cause Generalized Increased Neuronal Firing in Computer Simulations of

Ping Zheng, Ivan Soltesz, Robert J. Morgan, 2015 .

De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.

D. MacArthur, L. Vissers, M. Reijnders, 2016, American journal of human genetics.

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

Robert W. Taylor, H. Prokisch, M. Simpson, 2017, neurogenetics.

Pacemaker channel dysfunction in a patient with sinus node disease.

G. Breithardt, E. Schulze-Bahr, O. Pongs, 2003, The Journal of clinical investigation.

C-terminal HERG ( LQT 2 ) mutations disrupt

S. Priori, G. Mönnig, E. Schulze-Bahr, 2006 .

C-terminal HERG ( LQT2 ) mutations disrupt I Kr channel regulation through 14-3-3 e

S. Priori, G. Mönnig, E. Schulze-Bahr, 2006 .

Postsynaptic origin of CB1‐dependent tonic inhibition of GABA release at cholecystokinin‐positive basket cell to pyramidal cell synapses in the CA1 region of the rat hippocampus

I. Soltesz, Csaba Földy, A. Neu, 2007, The Journal of physiology.

L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.

A. Heerschap, F. Morellini, D. Isbrandt, 2013, Human molecular genetics.

Molecular mechanisms of glial swelling in vitro.

O. Kempski, A. Baethmann, F. Staub, 1988, Neurochemical pathology.

Cell Volume Regulation of Glial Cells During Anoxia and Hyposmotic Exposure In Vitro

O. Kempski, A. Baethmann, A. Neu, 1985 .

Presynaptic, Activity-Dependent Modulation of Cannabinoid Type 1 Receptor-Mediated Inhibition of GABA Release

I. Soltesz, Mathew V. Jones, Csaba Földy, 2006, The Journal of Neuroscience.

Prevention of Plasticity of Endocannabinoid Signaling Inhibits Persistent Limbic Hyperexcitability Caused by Developmental Seizures

Ivan Soltesz, Ken Mackie, Axel Neu, 2007, The Journal of Neuroscience.

Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure

C. Gerloff, E. Schwedhelm, D. Isbrandt, 2019, Amino Acids.

Loss of TNR causes a nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus

T. Strom, H. Venselaar, R. Maroofian, 2020, Genetics in Medicine.

Cloning and functional expression of rat ether‐à‐go‐go‐like K+ channel genes

O. Pongs, J. Ludwig, A. Neu, 1998, The Journal of physiology.

A Mouse Model of Creatine Transporter Deficiency Reveals Impaired Motor Function and Muscle Energy Metabolism

A. Heerschap, D. Isbrandt, I. Hermans-Borgmeyer, 2018, Front. Physiol..

Activation of GABAA Receptors by Guanidinoacetate: A Novel Pathophysiological Mechanism

Jochen Roeper, Dirk Isbrandt, Gerhard Trube, 2002, Neurobiology of Disease.

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease

Dirk Isbrandt, Matthias Paul, Eric Schulze-Bahr, 2010, Human mutation.

Loss of TNR causes a nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus

T. Strom, C. Kim, H. Venselaar, 2020, Genetics in Medicine.

Homeostatic Plasticity Studied Using In Vivo Hippocampal Activity-Blockade: Synaptic Scaling, Intrinsic Plasticity and Age-Dependence

Ivan Soltesz, Axel Neu, Julio C. Echegoyen, 2007, PloS one.

C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.

Dirk Isbrandt, Colleen E Clancy, Eric Schulze-Bahr, 2006, Human molecular genetics.

Creatine, guanidinoacetate and homoarginine in statin-induced myopathy

C. Gerloff, E. Schwedhelm, D. Isbrandt, 2020, Amino Acids.

Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure

C. Gerloff, E. Schwedhelm, D. Isbrandt, 2019, Amino Acids.