Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Melanie, Rammer"'
Autor:
Theodora Malli, Melanie Rammer, Sabrina Haslinger, Jonathan Burghofer, Sonja Burgstaller, Hans-Christian Boesmueller, Renate Marschon, Wolfgang Kranewitter, Martin Erdel, Sabine Deutschbauer, Gerald Webersinke
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Abstract Background Translocations of the IGH locus on 14q32.3 are present in about 8% of patients with chronic lymphocytic leukemia (CLL) and contribute to leukemogenesis by deregulating the expression of the IGH-partner genes. Identification of the
Externí odkaz:
https://doaj.org/article/9caff90d8fc94d6c995c5338a0baf292
Autor:
Gerald Webersinke, Jonathan Burghofer, Theodora Malli, Melanie Rammer, Stephan Wenzel Jahn, Axel Niendorf, Fattaneh A. Tavassoli, Farid Moinfar
Publikováno v:
Archives of Pathology & Laboratory Medicine.
Context.— Low-grade fibromatosis-like metaplastic carcinoma (FLMC) is a very rare subtype of triple-negative metaplastic (spindle cell) breast carcinoma. It is characterized by the proliferation of spindle cells closely resembling fibromatosis, whi
Autor:
Bernhard Haid, Melanie Rammer, Felix Nägele, Helga Fritsch, Jozsef Dudas, Elisabeth J. Pechriggl, Josef Oswald, Gerald Webersinke
Publikováno v:
Journal of pediatric urology. 16(1)
Summary Introduction Fibroblast growth factors (FGFs) play a crucial role in early embryogenesis of the genital tubercle and are involved in the development of hypospadias, affecting both endo- and ectodermally derived tissues. It was hypothesized th
Autor:
Florian Obermair, Wolfgang Kranewitter, Katharina Wimmer, Jonathan Burghofer, Anna Schossig, Melanie Rammer, Hans-Christoph Duba, Gerald Webersinke, Beate Mayrbaeurl, Theodora Malli
Publikováno v:
Familial cancer. 18(2)
Hereditary diffuse gastric cancer (HDGC) is an autosomal-dominantly inherited cancer syndrome associated with a high risk for diffuse gastric and lobular breast cancer, caused by heterozygous CDH1 germline mutations. Of note, also cleft lip/palate (C
Autor:
Renate Marschon, Martin Erdel, Hans-Christian Boesmueller, Sabrina Haslinger, Gerald Webersinke, Jonathan Burghofer, Wolfgang Kranewitter, Melanie Rammer, Sabine Deutschbauer, Theodora Malli, Sonja Burgstaller
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Background Translocations of the IGH locus on 14q32.3 are present in about 8% of patients with chronic lymphocytic leukemia (CLL) and contribute to leukemogenesis by deregulating the expression of the IGH-partner genes. Identification of these genes
Autor:
Gerald Webersinke, Wolfgang Kranewitter, Ingrid Simonitsch-Klupp, Peter Valent, Sabine Deutschbauer, Veronika Buxhofer-Ausch, Holger Rumpold, Melanie Rammer, Theodora Malli, Martin Erdel, Kirsten Muellner-Ammer, Thomas Birkner, Renate Marschon, Christian Sebesta
Publikováno v:
Genes, Chromosomes and Cancer. 55:60-68
Myeloid and lymphoid neoplasms with fibroblast growth factor receptor 1 (FGFR1) abnormalities, also known as 8p11 myeloproliferative syndrome (EMS), represent rare and aggressive disorders, associated with chromosomal aberrations that lead to the fus
Autor:
Hubert Hackl, Theodora Malli, Eva Maier, Pornpimol Charoentong, Holger Rumpold, Gerald Webersinke, Andreas L. Petzer, Sophie Haitchi-Petnehazy, Melanie Rammer, Maria Steinmair
Publikováno v:
Clinicalexperimental metastasis. 34(6-7)
Worldwide, colon cancer is among the most common cancer entities. Understanding the molecular background is the key to enable accurate stage determination, which is crucial to assess optimal therapy options. The search for preoperative biomarkers is
Autor:
Theodora, Malli, Veronika, Buxhofer-Ausch, Melanie, Rammer, Martin, Erdel, Wolfgang, Kranewitter, Holger, Rumpold, Renate, Marschon, Sabine, Deutschbauer, Ingrid, Simonitsch-Klupp, Peter, Valent, Kirsten, Muellner-Ammer, Christian, Sebesta, Thomas, Birkner, Gerald, Webersinke
Publikováno v:
Genes, chromosomescancer. 55(1)
Myeloid and lymphoid neoplasms with fibroblast growth factor receptor 1 (FGFR1) abnormalities, also known as 8p11 myeloproliferative syndrome (EMS), represent rare and aggressive disorders, associated with chromosomal aberrations that lead to the fus