Ralph Witzgall researcher
Witzgall, Ralph
VIAF ID: 58145971452032331636 (Personal)
Permalink: http://viaf.org/viaf/58145971452032331636
Preferred Forms
- 100 0 _ ‡a Ralph Witzgall ‡c researcher
- 100 1 _ ‡a Witzgall, Ralph
4xx's: Alternate Name Forms (4)
5xx's: Related Names (1)
Works
Title | Sources |
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Advanced electron microscopic techniques provide a deeper insight into the peculiar features of podocytes | |
Biodistribution of quantum dots in the kidney after intravenous injection | |
The calcium-activated chloride channel Anoctamin 1 contributes to the regulation of renal function | |
Calmodulin-dependent activation of the epithelial calcium-dependent chloride channel TMEM16A | |
Cytosolic phospholipase A2 (PLA2), but not secretory PLA2, potentiates hydrogen peroxide cytotoxicity in kidney epithelial cells | |
Differentiation and cell polarity during renal cyst formation in the Han:SPRD (cy/+) rat, a model for ADPKD. | |
Doxycycline accelerates renal cyst growth and fibrosis in the pcy/pcy mouse model of type 3 nephronophthisis, a form of recessive polycystic kidney disease. | |
An endocytosis defect as a possible cause of proteinuria in polycystic kidney disease | |
ER-localized bestrophin 1 activates Ca2+-dependent ion channels TMEM16A and SK4 possibly by acting as a counterion channel. | |
Expression of clusterin in Crohn's disease of the terminal ileum | |
Expression of the conjugate export pump encoded by the mrp2 gene in the apical membrane of kidney proximal tubules. | |
Genomic structure and chromosomal location of the rat gene encoding the zinc finger transcription factor Kid-1. | |
Identification and characterization of polycystin-2, the PKD2 gene product | |
Impaired endocytosis may represent an obstacle to gene therapy in polycystic kidney disease | |
Integration of Cistromic and Transcriptomic Analyses Identifies Nphs2, Mafb, and Magi2 as Wilms' Tumor 1 Target Genes in Podocyte Differentiation and Maintenance | |
Intravital Imaging Reveals Angiotensin II-Induced Transcytosis of Albumin by Podocytes. | |
Kid-1 expression is high in differentiated renal proximal tubule cells and suppressed in cyst epithelia. | |
Kidney podocytes as specific targets for cyclo(RGDfC)-modified nanoparticles. | |
Klonierung der [p-Untereinheit] des menschlichen IL-2-Rezeptors [IL-Rezeptors] Expression in Fibroblasten-Zellinien der Maus und Analyse des Expressionsverhaltens in Escherichia coli | |
The Krüppel-associated box-A (KRAB-A) domain of zinc finger proteins mediates transcriptional repression. | |
Lack of a laterality phenotype in Pkd1 knock-out embryos correlates with absence of polycystin-1 in nodal cilia | |
Lack of connexin 40 causes displacement of renin-producing cells from afferent arterioles to the extraglomerular mesangium | |
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes | |
LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys | |
Localization of proliferating cell nuclear antigen, vimentin, c-Fos, and clusterin in the postischemic kidney. Evidence for a heterogenous genetic response among nephron segments, and a large pool of mitotically active and dedifferentiated cells. | |
A mammalian expression vector for the expression of GAL4 fusion proteins with an epitope tag and histidine tail | |
Missense mutation in sterile alpha motif of novel protein SamCystin is associated with polycystic kidney disease in (cy/+) rat. | |
Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome | |
Mutant polycystin-2 induces proliferation in primary rat tubular epithelial cells in a STAT-1/p21-independent fashion accompanied instead by alterations in expression of p57KIP2 and Cdk2. | |
Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains. | |
Nail-patella syndrome | |
Natriuretic Peptide Receptor Guanylyl Cyclase-A in Podocytes is Renoprotective but Dispensable for Physiologic Renal Function. | |
New developments in the field of cystic kidney diseases. | |
NMR-assignments of a cytosolic domain of the C-terminus of polycystin-2 | |
Nonspecific cation current associated with native polycystin-2 in HEK-293 cells. | |
Novel role for polycystin-1 in modulating cell proliferation through calcium oscillations in kidney cells | |
Phospholipase A(2) and Lipids as Potential Modulators of c-Raf-1 Kinase | |
Phosphorylation of C-terminal polycystin-2 influences the interaction with PIGEA14: a QCM study based on solid supported membranes. | |
Photochemically Active Fluorophore-DNA/RNA Conjugates for Cellular Imaging of Nucleic Acids by Readout in Electron Microscopy | |
PIGEA-14, a novel coiled-coil protein affecting the intracellular distribution of polycystin-2 | |
The podocyte-specific inactivation of Lmx1b, Ldb1 and E2a yields new insight into a transcriptional network in podocytes. | |
Polycystic kidney disease--a tale of calcium channels and the actin cytoskeleton | |
Polycystin-1 promotes PKCalpha-mediated NF-kappaB activation in kidney cells | |
Polycystin-2--an intracellular or plasma membrane channel? | |
A polycystin-2 protein with modified channel properties leads to an increased diameter of renal tubules and to renal cysts | |
Polycystin-2 takes different routes to the somatic and ciliary plasma membrane | |
The proximal tubule phenotype and its disruption in acute renal failure and polycystic kidney disease. | |
Quantifying the interaction of the C-terminal regions of polycystin-2 and polycystin-1 attached to a lipid bilayer by means of QCM | |
The rat pkd2 protein assumes distinct subcellular distributions in different organs | |
Regulation of clusterin expression following spinal cord injury | |
Renal osmotic stress-induced cotransporter: expression in the newborn, adult and post-ischemic rat kidney. | |
Renal phenotype in heterozygous Lmx1b knockout mice (Lmx1b+/-) after unilateral nephrectomy | |
Soluble interleukin-2 receptors inhibit interleukin 2-dependent proliferation and cytotoxicity: explanation for diminished natural killer cell activity in cutaneous T-cell lymphomas in vivo? | |
The swelling-activated chloride channel ClC-2, the chloride channel ClC-3, and ClC-5, a chloride channel mutated in kidney stone disease, are expressed in distinct subpopulations of renal epithelial cells | |
A truncated polycystin-2 protein causes polycystic kidney disease and retinal degeneration in transgenic rats | |
Up-regulation of the human serum and glucocorticoid-dependent kinase 1 in glomerulonephritis | |
Use of the tetracycline system for inducible protein synthesis in the kidney |