M. Kann

发表

A Single-Cell Transcriptome Atlas of the Mouse Glomerulus.

Haiyue Liu, Nikolaus Rajewsky, Bernhard Schermer, 2018, Journal of the American Society of Nephrology : JASN.

[Genetics of dystonia].

X. Breakefield, P. Pramstaller, P. Vieregge, 2000, Der Nervenarzt.

Role of SCA2 mutations in early‐ and late‐onset dopa‐responsive parkinsonism

K. Marder, A. Lang, S. Fahn, 2002, Annals of neurology.

Parkin mutations in a patient with hemiparkinsonism–hemiatrophy: A clinical–genetic and PET study

C. Goetz, P. Pramstaller, P. Vieregge, 2002, Neurology.

The transcription factor sry‐related HMG box‐4 (SOX4) is required for normal renal development in vivo

Michel G. Arsenault, J. Ho, G. Wright, 2013, Developmental dynamics : an official publication of the American Association of Anatomists.

N-Degradomic Analysis Reveals a Proteolytic Network Processing the Podocyte Cytoskeleton.

Pitter F. Huesgen, Markus M. Rinschen, B. Schermer, 2017, Journal of the American Society of Nephrology : JASN.

Loss of genome maintenance accelerates podocyte damage

Victor G. Puelles, B. Schermer, T. Benzing, 2022, bioRxiv.

Inhibition of insulin/IGF-1 receptor signaling protects from mitochondria-mediated kidney failure

R. Müller, B. Schermer, T. Benzing, 2015, EMBO molecular medicine.

DEV119735 1254..1266

Markus M. Rinschen, B. Schermer, T. Benzing, 2015 .

Inversion Region for Hypertension and Brachydactyly on Chromosome 12p Features Multiple Splicing and Noncoding RNA

D. Chitayat, F. Luft, Y. Neuenfeld, 2008, Hypertension.

First use of the anti‐VWF nanobody caplacizumab to treat iTTP in pregnancy

T. Benzing, M. Thevis, B. Grüttner, 2021, British journal of haematology.

Parkin deletions in a family with adult‐onset, tremor‐dominant parkinsonism: Expanding the phenotype

X. Breakefield, P. Pramstaller, P. Vieregge, 2000, Annals of neurology.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Andreas Busjahn, Jens Jordan, Herbert Schulz, 2015, Nature Genetics.

A 1-year, randomized, placebo-controlled study of donepezil in patients with mild to moderate AD. Authors' reply

K. Marder, A. Lang, Juliette M. Harris, 2002 .

Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism

Christine Klein, Katja Hedrich, X. Breakefield, 2002, Annals of neurology.

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism.

A. Lang, X. Breakefield, P. Pramstaller, 2001, Human molecular genetics.

Combined Therapy with Intravenous Immunoglobulins, Letermovir and (Val-)Ganciclovir in Complicated Courses of CMV-Infection in Transplant Recipients

R. Kaiser, R. Müller, D. Stippel, 2021, Microorganisms.

Evaluation of 50 probands with early-onset Parkinson’s disease for Parkin mutations

K. Marder, S. Fahn, S. Bressman, 2002, Neurology.

DNA damage activates mTORC1 signaling in podocytes leading to glomerulosclerosis

Victor G. Puelles, B. Schermer, T. Benzing, 2020 .

Distribution, type, and origin of Parkin mutations: Review and case studies

K. Marder, A. Lang, Juliette M. Harris, 2004, Movement disorders : official journal of the Movement Disorder Society.

Frequency of parkin mutations in late‐onset Parkinson's disease

K. Marder, A. Lang, Juliette M. Harris, 2003, Annals of neurology.

Protein half‐life determines expression of proteostatic networks in podocyte differentiation

Markus M. Rinschen, B. Schermer, T. Benzing, 2018, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Quantitative deep mapping of the cultured podocyte proteome uncovers shifts in proteostatic mechanisms during differentiation.

Markus M. Rinschen, B. Schermer, T. Benzing, 2016, American journal of physiology. Cell physiology.

CALINCA—A Novel Pipeline for the Identification of lncRNAs in Podocyte Disease

C. Dieterich, R. Müller, B. Schermer, 2021, Cells.

Constitutive activation of the mTOR signaling pathway within the normal glomerulus.

G. McMahon, J. Kreidberg, J. Ho, 2012, Biochemical and biophysical research communications.

YAP-mediated mechanotransduction determines the podocyte’s response to damage

Markus M. Rinschen, B. Schermer, T. Benzing, 2017, Science Signaling.

WT1 targets Gas1 to maintain nephron progenitor cells by modulating FGF signals

Markus M. Rinschen, B. Schermer, T. Benzing, 2015, Development.

Genome-Wide Analysis of Wilms' Tumor 1-Controlled Gene Expression in Podocytes Reveals Key Regulatory Mechanisms.

P. Park, Y. L. Jung, B. Schermer, 2015, Journal of the American Society of Nephrology : JASN.

Individual nephron proteomes connect morphology and function in proteinuric kidney disease

Markus M. Rinschen, T. Reinheckel, A. Beyer, 2017, bioRxiv.

Hand-Assisted Retroperitoneoscopic Donor Nephrectomy Compared to Anterior Approach Open Donor Nephrectomy: Improved Long-Term Physical Component Score in Health-Related Quality of Life in Living Kidney Donors.

Michael N Thomas, M. Hellmich, R. Müller, 2020, Transplantation proceedings.

Loss of genome maintenance accelerates podocyte damage and aging

Victor G. Puelles, B. Schermer, T. Benzing, 2023, bioRxiv.

The parkin gene is not involved in late-onset Parkinson's disease.

K. Marder, A. Lang, S. Bressman, 2002, Neurology.

Monitoring of hepatitis E virus RNA during treatment for chronic hepatitis E virus infection after renal transplantation

R. Kaiser, T. Benzing, D. Stippel, 2021, Immunity, inflammation and disease.

DNA damage activates mTORC1 signaling in podocytes leading to glomerulosclerosis

Victor G. Puelles, B. Schermer, T. Benzing, 2020 .

Genome-Wide Analysis of Wilms' Tumor 1-Controlled Gene Expression in Podocytes Reveals Key Regulatory Mechanisms.

P. Park, Y. L. Jung, B. Schermer, 2015, Journal of the American Society of Nephrology : JASN.

Impact of first-line use of caplacizumab on treatment outcomes in immune thrombotic thrombocytopenic purpura.

A. Kribben, K. Schulmann, J. Gaedeke, 2022, Journal of thrombosis and haemostasis : JTH.