Joachim Schuster

发表

BRANCHED-CHAIN AMINOTRANSFERASE4 Is Part of the Chain Elongation Pathway in the Biosynthesis of Methionine-Derived Glucosinolates in Arabidopsis[W]

Stefan Binder, M. Reichelt, J. Gershenzon, 2006, The Plant Cell Online.

Branched‐chain amino acid metabolism in higher plants

S. Binder, Joachim Schuster, Tanja Knill, 2007 .

In Vivo Stability of Therapeutic Proteins

Joachim Schuster, P. Detampel, A. Koulov, 2020, Pharmaceutical Research.

Effect of High‐Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis

A. Winkler, J. Dreyhaupt, S. Petri, 2019, Annals of neurology.

The Branched-Chain Amino Acid Transaminase Gene Family in Arabidopsis Encodes Plastid and Mitochondrial Proteins 1

S. Binder, Joachim Schuster, R. Diebold, 2002 .

Tracking the physical stability of fluorescent-labeled mAbs under physiologic invitro conditions in human serum and PBS.

A. Racher, Joachim Schuster, P. Detampel, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Safety and efficacy of rasagiline as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a randomised, double-blind, parallel-group, placebo-controlled, phase 2 trial

S. Klebe, U. Bogdahn, A. Winkler, 2018, The Lancet Neurology.

Fat-rich versus carbohydrate-rich nutrition in ALS: a randomised controlled study

J. Dreyhaupt, A. Ludolph, Joachim Schuster, 2022, Journal of Neurology, Neurosurgery, and Psychiatry.

Effect of high-caloric nutrition on serum neurofilament light chain levels in amyotrophic lateral sclerosis

A. Winkler, J. Dreyhaupt, S. Petri, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.

H. Braak, T. Meitinger, P. Andersen, 2019, Brain : a journal of neurology.

Safety and efficacy of immunoadsorption versus plasma exchange in steroid-refractory relapse of multiple sclerosis and clinically isolated syndrome: A randomised, parallel-group, controlled trial

J. Dreyhaupt, A. Ludolph, Joachim Schuster, 2019, EClinicalMedicine.

Hot-spot KIF5A mutations cause familial ALS

H. Braak, T. Meitinger, T. Strom, 2018, Brain : a journal of neurology.

Arabidopsis Branched-Chain Aminotransferase 3 Functions in Both Amino Acid and Glucosinolate Biosynthesis1[W][OA]

M. Reichelt, J. Gershenzon, S. Binder, 2007, Plant Physiology.

The mitochondrial branched-chain aminotransferase (AtBCAT-1) is capable to initiate degradation of leucine, isoleucine and valine in almost all tissues in Arabidopsis thaliana

S. Binder, Joachim Schuster, 2004, Plant Molecular Biology.

The Branched-Chain Amino Acid Transaminase Gene Family in Arabidopsis Encodes Plastid and Mitochondrial Proteins1

Stefan Binder, S. Binder, Joachim Schuster, 2002, Plant Physiology.

Stability of Monoclonal Antibodies after Simulated Subcutaneous Administration.

Joachim Schuster, J. Huwyler, R. Mathaes, 2021, Journal of pharmaceutical sciences.

Comprehensive analysis of the mutation spectrum in 301 German ALS families

S. Klebe, T. Meitinger, T. Strom, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Assessment of Antibody Stability in a Novel Protein-Free Serum Model

Joachim Schuster, R. Mathaes, Vinay Kamuju, 2021, Pharmaceutics.

Analytical Challenges Assessing Protein Aggregation and Fragmentation Under Physiologic Conditions.

Joachim Schuster, J. Huwyler, R. Mathaes, 2021, Journal of pharmaceutical sciences.

The Europeanisation of Industrial Relations: National and European Processes in Germany, UK, Italy and France

Joachim Schuster, J. Tholen, L. Fulton, 2002 .

Fate of Antibody and Polysorbate Particles in a Human Serum Model.

Joachim Schuster, R. Mathaes, Vinay Kamuju, 2021, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

In Vivo Stability of Therapeutic Proteins

Joachim Schuster, P. Detampel, A. Koulov, 2020, Pharmaceutical Research.

Pharyngeal electrical stimulation in amyotrophic lateral sclerosis: a pilot study

A. Ludolph, Joachim Schuster, J. Dorst, 2022, Therapeutic advances in neurological disorders.

ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale

S. Petri, A. Ludolph, J. Grosskreutz, 2022, Neurological research and practice.

Neurofilament light and heterogeneity of disease progression in amyotrophic lateral sclerosis: development and validation of a prediction model to improve interventional trials

V. Meininger, S. Anders, D. Devos, 2021, Translational neurodegeneration.

Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations

D. Lulé, S. Petri, J. Grosskreutz, 2023, Brain communications.

Phenotyping of the thoracic-onset variant of amyotrophic lateral sclerosis

G. Nagel, D. Rothenbacher, A. Ludolph, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

Prognostic factors in ALS: a comparison between Germany and China

A. Winkler, J. Dreyhaupt, S. Petri, 2019, Journal of Neurology.

Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriers

P. Andersen, J. Kassubek, Joachim Schuster, 2023, EBioMedicine.

Protein Stability After Administration: A Physiologic Consideration.

Joachim Schuster, R. Mathaes, Vinay Kamuju, 2022, Journal of pharmaceutical sciences.

Particle Analysis of Biotherapeutics in Human Serum using Machine Learning.

Kai D. Schleicher, Joachim Schuster, J. Huwyler, 2020, Journal of pharmaceutical sciences.

Longitudinal course of neurofilament light chain levels in amyotrophic lateral sclerosis—insights from a completed randomized controlled trial with rasagiline

J. Statland, Joachim Schuster, J. Dorst, 2023, European journal of neurology.

Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis

S. Petri, J. Grosskreutz, Joachim Schuster, 2023, Brain communications.