Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Peter Herter"'
Autor:
Heinz-Herbert Homann, Oliver Müller, Cornelius Kuhnen, C. Lanckohr, M. Lehnhardt, Maria Debiec-Rychter, Peter Herter
Publikováno v:
Der Pathologe. 31:97-105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f23aacd778e18a01e4136849d38453bd
https://doi.org/10.1007/s00292-009-1260-y
https://doi.org/10.1007/s00292-009-1260-y
Autor:
Cornelius Kuhnen, Heinz-Herbert Homann, Marcus Lehnhardt, Peter Herter, Oliver Müller, Alice Kasprzynski, C. Lanckohr, Ludger Klein-Hitpass
Publikováno v:
Der Pathologe. 31:60-66
Myxoid-rundzellige Liposarkome (LS) sind durch typische chromosomale Translokationen charakterisiert. Hierdurch konnten fur diese Tumorentitat charakteristische Genexpressionsmuster resultieren. Zur Identifikation uberexprimierter Gene in myxoid-rund
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48167182b392ba09867af50673786e2b
https://doi.org/10.1007/s00292-009-1234-0
https://doi.org/10.1007/s00292-009-1234-0
Autor:
Malgorzata Jaworska, Ivo Leuschner, Thomas Mentzel, Cornelius Kuhnen, Daniel Druecke, Georg Johnen, Peter Herter
Publikováno v:
Virchows Archiv. 449:572-578
Sclerosing (pseudovascular) rhabdomyosarcoma in adults has been described as a rare variant of rhabdomyosarcoma characterized by extensive hyaline fibrosis and pseudovascular growth patterns. We describe another case of this rhabdomyosarcoma subtype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bfd4155ec08b4e6e8add4f8249ed837
https://doi.org/10.1007/s00428-006-0282-6
https://doi.org/10.1007/s00428-006-0282-6
Autor:
Cornelius Kuhnen, Alice Kasprzynski, Georg Johnen, P. M. Vogt, Peter Herter, Malgorzata Jaworska
Publikováno v:
Der Pathologe. 26:331-338
Der Fall eines Myoepithelioms des tiefen Weichgewebes wird mit klinisch-pathologischen, ultrastrukturellen und genetischen Befunden vorgestellt. Bei einem 30-jahrigen Patienten fand sich ein Weichgewebstumor am rechten Unterschenkel innerhalb der tie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e7f882ff68af47429fa2f8fe7c12cfb
https://doi.org/10.1007/s00292-005-0773-2
https://doi.org/10.1007/s00292-005-0773-2
Publikováno v:
Der Pathologe. 26:96-110
Morphological, ultrastructural, and immunohistochemical findings of 12 diffuse type-tenosynovial giant cell tumors/pigmented villonodular synovitis are presented compared to 30 localized tenosynovial giant cell tumors (giant cell tumor of tendon shea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f11c72113a67d9110b9c72a0861ec83
https://doi.org/10.1007/s00292-004-0740-3
https://doi.org/10.1007/s00292-004-0740-3
Autor:
Inko Nimmrich, Oliver Müller, Matthias Renner, Slava Chtarbova, Silke Erdmann, Peter Herter, Jan Kitajewski
Publikováno v:
Biochemical Journal. 367:723-728
The Wnt signal transduction pathway regulates morphogenesis and mitogenesis of cells in multicellular organisms. A major downstream consequence of Wnt-1 signalling is the activation of β-catenin/T-cell factor (TCF)-mediated transcription. We compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6170aec8a756372dfcf8603e219cc3bd
https://doi.org/10.1042/bj20020699
https://doi.org/10.1042/bj20020699
Autor:
Eberhard Schlatter, Erik Harms, Robert Kleta, Ibrahim Çetinkaya, Peter Herter, Jochen R. Hirsch
Publikováno v:
Journal of the American Society of Nephrology. 13:2085-2093
Cystinosis is the most common cause of the renal Fanconi syndrome in children, leading to severe electrolyte disturbances and growth failure. A defective lysosomal transporter, cystinosin, results in intralysosomal accumulation of cystine. Loading ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce316689a11f02a4af4173a304b3e80d
https://doi.org/10.1097/01.asn.0000023681.13865.25
https://doi.org/10.1097/01.asn.0000023681.13865.25
Publikováno v:
Journal of Biological Chemistry. 277:7831-7837
Small GTPases of the Ras family are major players of signal transduction in eukaryotic cells. They receive signals from a number of receptors and transmit them to a variety of effectors. The distribution of signals to different effector molecules all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0213dd2cdd093dd559062bfabb38d1a
https://doi.org/10.1074/jbc.m110800200
https://doi.org/10.1074/jbc.m110800200
Autor:
Klaus-Michael Müller, Dirk Martin, Gert Muhr, Matthias Soddemann, Peter Herter, Sabine Kahmann, Cornelius Kuhnen, Oliver Müller
Publikováno v:
Human Mutation. 19:165-172
A new method for mutation detection is described, which is a technical advancement of the protein truncation test. The new technique is non-radioactive and highly sensitive for detection of virtually all sequence mutations, which lead to a stop signa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62f189c96a219e4bb145fb685c3d48e0
https://doi.org/10.1002/humu.10024
https://doi.org/10.1002/humu.10024
Publikováno v:
Pathology Research and Practice
In the spectrum of neurofibromas, pigmented tumors are rare variants usually showing only faint, macroscopically obvious pigmentation. We report a case of a huge pigmented neurofibroma with extended, macroscopically striking pigmentation in a patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb428e4c5ea562bc0f2957d4eb89e41
https://doi.org/10.1078/0344-0338-00199
https://doi.org/10.1078/0344-0338-00199