C. Dafinger

发表

Jade-1S phosphorylation induced by CK1α contributes to cell cycle progression

Markus M. Rinschen, B. Schermer, T. Benzing, 2016, Cell cycle.

Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases

D. Haffner, M. Liebau, C. Bergmann, 2022, Orphanet Journal of Rare Diseases.

The carboxy‐terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC‐activation

B. Schermer, T. Benzing, T. Weimbs, 2020, Journal of cellular and molecular medicine.

Challenges in establishing genotype–phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations

B. Schermer, T. Benzing, K. Zerres, 2017, Pediatric Nephrology.

Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics.

H. Zentgraf, I. Ebermann, H. Bolz, 2011, The Journal of clinical investigation.

IL‐6/Smad2 signaling mediates acute kidney injury and regeneration in a murine model of neonatal hyperoxia

M. Liebau, J. Dötsch, K. Dinger, 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Casein Kinase 1 α Phosphorylates the Wnt Regulator Jade-1 and Modulates Its Activity*

Markus M. Rinschen, B. Schermer, T. Benzing, 2014, The Journal of Biological Chemistry.

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

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

Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling

B. Schermer, L. Weber, H. Thiele, 2021, Kidney international reports.

Neph2/Kirrel3 regulates sensory input, motor coordination, and home‐cage activity in rodents

B. Schermer, T. Benzing, A. Bilkei-Gorzo, 2018, Genes, brain, and behavior.

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality

B. Schermer, T. Benzing, M. Liebau, 2021, Molecular and Cellular Pediatrics.

Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT)

R. Müller, B. Schermer, T. Benzing, 2013, Journal of Molecular Medicine.

Primary cilia suppress Ripk3-mediated necroptosis

B. Schermer, T. Benzing, G. Slaats, 2022, Cell Death Discovery.

Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus

Markus M. Rinschen, M. Rauh, R. Müller, 2018, Experimental & Molecular Medicine.

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.

Monte Westerfield, Peter Nürnberg, Bernhard Schermer, 2010, The Journal of clinical investigation.

Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

H. Bolz, A. Koschak, S. Baig, 2011, Nature Neuroscience.

Loss of Dgcr8-mediated microRNA expression in the kidney results in hydronephrosis and renal malformation

R. Müller, B. Schermer, T. Benzing, 2015, BMC Nephrology.

The Ciliary Protein Nephrocystin-4 Translocates the Canonical Wnt Regulator Jade-1 to the Nucleus to Negatively Regulate β-Catenin Signaling*

B. Schermer, T. Benzing, M. Liebau, 2012, The Journal of Biological Chemistry.

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, 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.

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

K. Zerres, L. Weber, D. Mekahli, 2021, Kidney international.

Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3

Carsten Bergmann, Peter Nürnberg, Ahmad Mansour, 2012, Orphanet Journal of Rare Diseases.

Characterization of Three Ammonium Transporters of the Glomeromycotan Fungus Geosiphon pyriformis

A. Brachmann, A. Schüßler, Friedemann Loos, 2013, Eukaryotic Cell.

Characterization of three ammonium transporters of the

A. Brachmann, Friedemann Loos, D. Brucker, 2013 .

mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, bioRxiv.

Nephrocystin-4 Regulates Pyk2-induced Tyrosine Phosphorylation of Nephrocystin-1 to Control Targeting to Monocilia*

H. Zentgraf, R. Müller, B. Schermer, 2011, The Journal of Biological Chemistry.

The effect of mycophenolate mofetil on podocytes in nephrotoxic serum nephritis

R. Müller, B. Schermer, L. Weber, 2023, Scientific reports.

Magnetic resonance T2 mapping and diffusion-weighted imaging for early detection of cystogenesis and response to therapy in a mouse model of polycystic kidney disease.

D. Maintz, B. Schermer, T. Benzing, 2017, Kidney international.