Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Knut Dietzmann"'
Autor:
Dimitrios Kanakis, Uwe Lendeckel, Paraskevi Theodosiou, Henrik Dobrowolny, Christian Mawrin, Gerburg Keilhoff, Alicia Bukowska, Knut Dietzmann, Bernhard Bogerts, Hans-Gert Bernstein
Publikováno v:
Disease Markers, Vol 34, Iss 2, Pp 81-91 (2013)
Disease markers
Disease markers
ADAM 12 (meltrin alpha) belongs to a large family of molecules, consisting of members with both disintegrin and metalloproteinase properties. ADAMs have been implicated in several cell physiological processes including cell adhesion, cell fusion, pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6284d008c5cce8e37c75b4094f21c4a
https://doaj.org/article/333bdb72ae084c56806063146d5561ab
https://doaj.org/article/333bdb72ae084c56806063146d5561ab
Autor:
Thomas Kapapa, Raimund Firsching, Dieter Woischneck, M. Skalaj, Knut Dietzmann, S. Reissberg, B. Peters
Publikováno v:
Intensivmedizin und Notfallmedizin. 47:59-64
Fur Patienten mit einem nach schwerem Schadel-Hirn-Trauma (SHT) todlichen Verlauf gelten folgende Todesursachen als haufig: die supratentorielle Herniation, der diffuse axonale Hirnschaden und extrazerebrale Komplikationen. Diese seit Jahrzehnten ane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d274f2ad2ccadd430ec81d950f2dec92
https://doi.org/10.1007/s00390-009-0045-0
https://doi.org/10.1007/s00390-009-0045-0
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 118:121-126
The reasons for the increase of pituitary tumor-transforming gene (PTTG) transcripts in about 90% of pituitary adenomas are still not fully understood, although upregulation by basic fibroblast growth factor (bFGF) has been discussed as a potential c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e15dea022bf63fc376b2096b2ceff651
https://doi.org/10.1055/s-0029-1215588
https://doi.org/10.1055/s-0029-1215588
Autor:
Bernd Freigang, Knut Dietzmann, Christian Mawrin, Kathrin Chamaon, Mathias Löttrich, Elmar Kirches
Publikováno v:
Pathology - Research and Practice. 203:245-249
Expression of the transforming growth factor-beta (TGF-beta) protein family in the peripheral nervous system is well established, but the role of their cognate receptors TGF-beta receptor type 1 (R1) and type 2 (R2) has been less well studied. TGF-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e448e023a23d87a275da32f8567b8ea
https://doi.org/10.1016/j.prp.2006.12.007
https://doi.org/10.1016/j.prp.2006.12.007
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 38:610-620
The transmembrane tyrosine-specific protein kinase TrkB has been shown to serve as a receptor for the neurotrophic factors BDNF and NT-4. Neurotrophin binding to TrkB isoformes mediates many intracellular signaling pathways, including calcium signall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5dd14141bdcb5ac33968a7ad02b6569
https://doi.org/10.1016/j.biocel.2005.10.024
https://doi.org/10.1016/j.biocel.2005.10.024
Autor:
Christian Mawrin, Uwe Lendeckel, Anja Hellwig-Patyk, Arie Perry, Stefan Schulz, Guy Lindberg, Raimund Firsching, Kirsten Grimm, Albert Roessner, Elmar Kirches, Gerburg Keilhoff, Bernd W. Scheithauer, Knut Dietzmann, Christian K. Vorwerk, David H. Gutmann
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 64:1080-1088
Although somatostatin receptors have been detected in many normal and neoplastic tissues, little is known of their expression and function in peripheral nerve tumors. In the present study, we examined the expression of all 5 somatostatin receptor sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d210fb0b7bb01a5fee03215183701a
https://doi.org/10.1097/01.jnen.0000190065.36182.25
https://doi.org/10.1097/01.jnen.0000190065.36182.25
Publikováno v:
Biochemical and Biophysical Research Communications. 332:43-49
A heterogeneous group of multisystem disorders affecting various tissues and often including neuromuscular symptoms is caused by mutations of the mitochondrial genome, which codes 13 polypeptides of oxidative phosphorylation (OXPHOS) complexes and 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa7e6d987bb0efff455fab7afa9e438
https://doi.org/10.1016/j.bbrc.2005.04.086
https://doi.org/10.1016/j.bbrc.2005.04.086
Autor:
Antje Bornemann, Raimund Firsching, Bernd Sellhaus, Andreas von Deimling, Bernd F. M. Romeike, Thomas Schneider, Christian Mawrin, Falk R. Wiedemann, Knut Dietzmann
Publikováno v:
Journal of Neuro-Oncology. 73:109-115
Gliomatosis cerebri (GC) is a rare brain tumor characterized by widespread infiltration of large parts of the brain and sometimes even the spinal cord. To determine the cause of this extraordinary degree of brain invasion, we studied immunoexpression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::565855fe588a51e50e37974cb520088c
https://doi.org/10.1007/s11060-004-4206-5
https://doi.org/10.1007/s11060-004-4206-5
Autor:
Knut Dietzmann, Christian Mawrin, Dimitrios Kanakis, Stefan Braeuninger, Kathrin Chamaon, Elmar Kirches
Publikováno v:
Biochemical and Biophysical Research Communications. 331:86-92
The reasons for overexpression of the oncogene pituitary tumor transforming gene (PTTG) in tumors are still not fully understood. A possible influence of the insulin-like growth factor I (Igf-I) may be of interest, since enhanced Igf-I signalling was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e96fc91a5fd167dad33efd21db4fb3d3
https://doi.org/10.1016/j.bbrc.2005.03.124
https://doi.org/10.1016/j.bbrc.2005.03.124
Autor:
Christian, Mawrin, Elmar, Kirches, Regine, Schneider-Stock, Carsten, Boltze, Christian K, Vorwerk, Andreas, von Mawrin, Andreas, von Deimling, Gisela, Stoltenburg-Didinge, Antje, Bornemann, Bernd, Romeike, Bernd, Sellhaus, Knut, Dietzmann
Publikováno v:
Journal of Neuro-Oncology. 72:115-122
Gliomatosis cerebri (GC) is regarded as a rare glial neoplasm of unknown origin, and a detailed analysis of molecular alterations underlying this disease has started only recently. However, because GC characteristically affects large parts of the bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e1bcd6b2f59e0e25d356decb7fb09f3
https://doi.org/10.1007/s11060-004-2061-z
https://doi.org/10.1007/s11060-004-2061-z