Gärtner, Jutta

Inspiration is the major regulator of human CSF flow.

Dreha-Kulaczewski, S., Joseph, A. A., Merboldt, K.-D., Ludwig, H.-C., Gärtner, J., & Frahm, J. (2015) · The Journal of Neuroscience

Cerebrospinal fluid and hydrocephalusAdvanced MRI Techniques and Applications

Cited by 405

Anti-myelin oligodendrocyte glycoprotein antibodies in pediatric patients with optic neuritis

Rostasy, K., Mader, S., Schanda, K., Huppke, P., Gärtner, J., Kraus, V., Karenfort, M., Tibussek, D., Blaschek, A., Bajer-Kornek, B., et al. (2012) · Archives of Neurology

Multiple Sclerosis Research StudiesOcular Diseases and Behçet’s Syndrome

Cited by 182

Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals

Schueren, F., Lingner, T., George, R., Hofhuis, J., Dickel, C., Gärtner, J., & Thoms, S. (2014) · eLife

RNA and protein synthesis mechanismsRedox biology and oxidative stress

Cited by 180

Peroxisomes are juxtaposed to strategic sites on mitochondria

Cohen, Y., Klug, Y. A., Dimitrov, L., Erez, Z., Chuartzman, S. G., Elinger, D., Yofe, I., Soliman, K., Gärtner, J., Thoms, S., et al. (2014) · Molecular BioSystems

Fungal and yeast genetics researchAutophagy in Disease and Therapy

Cited by 117

Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders

Poll-The, B. T., & Gärtner, J. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 85

The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code

Hofhuis, J., Schueren, F., Nötzel, C., Lingner, T., Gärtner, J., Jahn, O., & Thoms, S. (2016) · Open Biology

RNA and protein synthesis mechanismsRNA Research and Splicing

Cited by 59

Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients

Weller, S., Rosewich, H., & Gärtner, J. (2008) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersFetal and Pediatric Neurological Disorders

Cited by 58

Live Cell FRET Microscopy

Hillebrand, M., Verrier, S. E., Ohlenbusch, A., Schäfer, A., Söling, H.-D., Wouters, F. S., & Gärtner, J. (2007) · Journal of Biological Chemistry

Metabolism and Genetic DisordersDrug Transport and Resistance Mechanisms

Cited by 54

Characterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transporters

Roerig, P., Mayerhofer, P., Holzinger, A., & Gärtner, J. (2001) · FEBS Letters

Metabolism and Genetic DisordersDrug Transport and Resistance Mechanisms

Cited by 40

Leukoencephalopathy and early death associated with an Ashkenazi-Jewish founder mutation in the Hikeshi gene

Edvardson, S., Kose, S., Jalas, C., Fattal-Valevski, A., Watanabe, A., Ogawa, Y., Mamada, H., Fedick, A. M., Ben-Shachar, S., Treff, N. R., et al. (2016) · Journal of Medical Genetics

Hereditary Neurological DisordersHeat shock proteins research

Cited by 33

Concurrent axon and myelin destruction differentiates X-linked adrenoleukodystrophy from multiple sclerosis

Bergner, C. G., Genc, N., Hametner, S., Franz, J., van der Meer, F., Mitkovski, M., Weber, M. S., Stoltenburg‐Didinger, G., Kühl, J., Köhler, W., et al. (2021) · Glia

Multiple Sclerosis Research StudiesLysosomal Storage Disorders Research

Cited by 23

Functional characterization of the adrenoleukodystrophy protein (ALDP) and disease pathogenesis

Gärtner, J., Dehmel, T., Klusmann, A., & Roerig, P. (2002) · Endocrine Research

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 15