M. Bauer

发表

Rapid determination of total homocysteine in blood spots by liquid chromatography-electrospray ionization-tandem mass spectrometry.

K. Gempel, K. Gerbitz, B. Casetta, 2000, Clinical chemistry.

The molecular basis of the Rhesus antigen Ew

M. Bauer, F. Noizat‐Pirenne, J. Cartron, 2004, Transfusion.

Import of proteins into mitochondria: A novel pathomechanism for progressive neurodegeneration

M. Bauer, W. Neupert, Walter Neupert, 2001, Journal of Inherited Metabolic Disease.

Protein Import Across the Inner Mitochondrial Membrane

M. Bauer, W. Neupert, M. Brunner, 1996 .

Chapter 33 Protein transport across the outer and inner membranes of mitochondria

M. Bauer, W. Neupert, 1996 .

Tim23 Links the Inner and Outer Mitochondrial Membranes

M. Bauer, W. Neupert, M. Brunner, 2000, Cell.

Role of the Deafness Dystonia Peptide 1 (DDP1) in Import of Human Tim23 into the Inner Membrane of Mitochondria*

K. Gerbitz, M. Bauer, W. Neupert, 2001, The Journal of Biological Chemistry.

Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry

K. Gempel, K. Gerbitz, M. Bauer, 2001, Journal of Inherited Metabolic Disease.

Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product.

K. Gerbitz, M. Bauer, S. Hofmann, 2003, Human molecular genetics.

Significance of Respirasomes for the Assembly/Stability of Human Respiratory Chain Complex I*

M. Bauer, H. Schägger, S. Hofmann, 2004, Journal of Biological Chemistry.

Functional and mutational characterization of human MIA40 acting during import into the mitochondrial intermembrane space.

M. Bauer, U. Rothbauer, S. Hofmann, 2005, Journal of molecular biology.

Protein translocation into mammalian mitochondria and its role in the development of human mitochondrial disorders

M. Bauer, S. Hofmann, 2004 .

Biogenesis of Tim23 and Tim17, integral components of the TIM machinery for matrix‐targeted preproteins

M. Bauer, W. Neupert, M. Brunner, 1998, The EMBO journal.

Leigh-like subacute necrotising encephalopathy in Yorkshire Terriers: neuropathological characterisation, respiratory chain activities and mitochondrial DNA

M. Bauer, S. Hofmann, K. Matiasek, 2009, Acta Neuropathologica.

Wolfram syndrome‐associated mutations lead to instability and proteasomal degradation of wolframin

M. Bauer, S. Hofmann, 2006, FEBS letters.

Association between infectious burden, socioeconomic status, and ischemic stroke.

H. Becher, M. Bauer, A. Grau, 2016, Atherosclerosis.

Multicenter Evaluation of a Fully Automated High-Throughput SARS-CoV-2 Antigen Immunoassay

M. Bauer, M. Lütgehetmann, Dominik Nörz, 2021, Infectious Diseases and Therapy.

"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old child

K. Gempel, K. Gerbitz, M. Bauer, 2001, European Journal of Pediatrics.

Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology*

S. Duvezin-Caubet, R. Jagasia, A. Reichert, 2006, Journal of Biological Chemistry.

Yeast mitochondrial F1F0‐ATPase: the novel subunit e is identical to Tim11

M. Bauer, W. Neupert, R. Stuart, 1997, FEBS letters.

Role of Tim23 as Voltage Sensor and Presequence Receptor in Protein Import into Mitochondria

M. Bauer, W. Neupert, M. Brunner, 1996, Cell.

Mitochondrial Disorders. A Diagnostic Challenge in Clinical Chemistry

K. Gempel, K. Gerbitz, M. Bauer, 1999, Clinical chemistry and laboratory medicine.

The MIM complex mediates preprotein translocationacross the mitochondrial inner membrane and couples it to the mt-Hsp70/ATP driving system

Walter Neupert, Michael Brunner, Hans-Christoph Schneider, 1995, Cell.

Mitochondrial Hsp70/MIM44 complex facilitates protein import

M. Bauer, W. Neupert, K. Dietmeier, 1994, Nature.

Functional Cooperation and Stoichiometry of Protein Translocases of the Outer and Inner Membranes of Mitochondria*

M. Bauer, W. Neupert, M. Brunner, 1997, The Journal of Biological Chemistry.

Clinical and molecular ® ndings in a patient with a novel mutation in the deafness ± dystonia peptide ( DDP 1 ) gene

M. Hennerici, J. Krauss, M. Bauer, 2022 .

Mitochondrial dysfunction in diabetes mellitus

K. Gerbitz, M. Bauer, S. Hofmann, 2001 .

The role of the TIM8–13 complex in the import of Tim23 into mitochondria

M. Bauer, W. Neupert, K. Káldi, 2000, EMBO Journal.

Tandem mass spectrometric assay for the determination of carnitine palmitoyltransferase II activity in muscle tissue.

K. Gempel, K. Gerbitz, M. Bauer, 2002, Analytical biochemistry.

Screening for Carnitine Palmitoyltransferase II Deficiency by Tandem Mass Spectrometry

S. Kiechl, J. Willeit, K. Gempel, 2002, Journal of Inherited Metabolic Disease.

Import of carrier proteins into the mitochondrial inner membrane mediated by Tim22

M. Bauer, W. Neupert, M. Brunner, 1996, Nature.

Organization and Function of the Small Tim Complexes Acting along the Import Pathway of Metabolite Carriers into Mammalian Mitochondria*

M. Bauer, U. Rothbauer, S. Hofmann, 2004, Journal of Biological Chemistry.

The C66W Mutation in the Deafness Dystonia Peptide 1 (DDP1) Affects the Formation of Functional DDP1·TIM13 Complexes in the Mitochondrial Intermembrane Space*

K. Gerbitz, M. Bauer, W. Neupert, 2002, The Journal of Biological Chemistry.

Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene.

M. Hennerici, J. Krauss, J. Wöhrle, 2003, Brain : a journal of neurology.

Mitochondrial Function and Biogenesis

M. Bauer, C. Koehler, 2004, Topics in Current Genetics.

Genetics of Mitochondria-Related Forms of Syndromic Diabetes Mellitus

K. Gerbitz, M. Bauer, S. Hofmann, 2001 .

A new mitochondrial point mutation in the transfer RNALys gene associated with progressive external ophthalmoplegia with impaired respiratory regulation

M. Bauer, A. Grau, M. Mörl, 2012, Journal of the Neurological Sciences.

Mixed chemodectoma-ganglioneuroma of the conus medullaris region

M. Bauer, K. Wurster, K. Parsch, 2004, Acta Neuropathologica.

Protein translocation into mitochondria: the role of TIM complexes.

M. Bauer, W. Neupert, M. Brunner, 2000, Trends in cell biology.

Adult carnitine palmitoyltransferase II deficiency: Detection of characteristic carnitine esters in serum by tandem mass spectrometry

K. Gempel, K. Gerbitz, M. Bauer, 1999, Journal of Inherited Metabolic Disease.

Dystonia in the Mohr–Tranebjaerg syndrome responds to GABAergic substances

M. Hennerici, J. Krauss, J. Wöhrle, 2004, Movement disorders : official journal of the Movement Disorder Society.

Genetic and structural characterization of the human mitochondrial inner membrane translocase.

A. Reichert, K. Gempel, K. Gerbitz, 1999, Journal of molecular biology.