Peter Herter
Max Planck Society
34 Papers
551 Citations
Peter Herter is an academic researcher from Max Planck Society. The author has contributed to research in topics: Cotransporter & Adenomatous polyposis coli. The author has an hindex of 19, co-authored 34 publications. Previous affiliations of Peter Herter include University of Regensburg.
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Papers
A simplified method for isolation of large numbers of defined nephron segments
TL;DR: A simplified method for the isolation of large numbers of nephron segments from rat and rabbit kidneys that maintains their normal architecture and a distinct separation of apical and basolateral membranes is described.
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The APC protein binds to A/T rich DNA sequences.
J. Deka,Peter Herter,Markus Sprenger-Haussels,S. Koosch,D. Franz,Klaus-Michael Müller,Cornelius Kuhnen,Ingrid Hoffmann,Oliver Müller +8 more
TL;DR: It is demonstrated that the nuclear APC protein level is high in cells in the basal crypt region of the normal colorectal epithelium, and staining resembles the staining pattern of a nuclear proliferation marker.
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Beta-catenin in soft tissue sarcomas: expression is related to proliferative activity in high-grade sarcomas.
Cornelius Kuhnen,Peter Herter,Oliver Müller,T. Muehlberger,Larissa Krause,Heinz H. Homann,Hans U. Steinau,Klaus-Michael Müller +7 more
TL;DR: Besides its role in cell adhesion, β-catenin exerts a function as an oncoprotein in sarcomas with intracytoplasmic and nuclear localization with binding to nuclear DNA and a previously discussed stimulation of cell proliferation caused by an increased β- catenin level can be postulated for high-grade soft tissue sarcoma in correlation with the rate of proliferation.
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Intracellular distribution of beta-catenin in colorectal adenomas, carcinomas and Peutz-Jeghers polyps.
TL;DR: The results point to an extensive redistribution of β-catenin, which starts early in colorectal tumorigenesis, and could serve as a criterion for estimating the malignant potential in the clinico-pathological evaluation of colon tumors during their early progression.
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Different modes of sodium-D-glucose cotransporter-mediated D-glucose uptake regulation in Caco-2 cells
Saeed Khoursandi,Daniel Scharlau,Peter Herter,Cornelius Kuhnen,Dirk Martin,Rolf K. H. Kinne,Helmut Kipp +6 more
TL;DR: Results suggest that, pharmacologically, d-glucose uptake can be regulated by a shift of SGLT1 between the plasma membrane and the endosomal pool; however, regulation by the physiological substrate d- glucose can be explained only by an alternative mechanism.
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