Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Walter Zumkeller"'
Autor:
Walter Zumkeller
Publikováno v:
Sarcoma, Vol 2, Iss 2, Pp 69-76 (1998)
Purpose/Results. Although surgical, chemo- and radiotherapeutic treatment regimens in patients with soft tissue sarcomas have constantly been refined over the past two decades, the survival rate for these patients is rather low.
Externí odkaz:
https://doaj.org/article/abd802c19de64766a2d7e10882e6260a
Autor:
Anita Heller, Petra Muschke, Thomas Liehr, Markus Stumm, Marianne Volleth, Walter Zumkeller, Peter Wieacker, Holger Tönnies
Publikováno v:
American Journal of Medical Genetics Part A. :261-264
Reports on patients with pure and complete trisomy 12p are rare. Up to now, 12 cases have been described in the literature. Here, we report on the genotype/phenotype-correlation of a female patient with a pure trisomy 12p. Conventional cytogenetic st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e1aa10fe6d16fb3b2f3170ff2ebf3d1
https://doi.org/10.1002/ajmg.a.30125
https://doi.org/10.1002/ajmg.a.30125
Autor:
Gudrun A. Rappold, Maki Fukami, Thomas Reinehr, Simone Schiller, Udo Heinrich, Elpis Vlachopapadoupoulou, Kazumichi Onigata, Walter Zumkeller, Markus Bettendorf, Tsutomu Ogata, Beate Niesler
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:1402-1406
Short stature, with an incidence of 3 in 100, is a fairly frequent disorder in children. Idiopathic short stature refers to patients who are short due to various unknown reasons. Mutations of a human homeobox gene, SHOX (short stature homeobox), have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27860118e10f7d70015fbcc931890ba4
https://doi.org/10.1210/jcem.87.3.8328
https://doi.org/10.1210/jcem.87.3.8328
Autor:
Manfred Westphal, Frank Berthold, Dorothea Zirkel, Dirk van den Boom, Hubert Köster, Manfred Schwab, Sabine Müller, Walter Zumkeller
Publikováno v:
Human Molecular Genetics. 9:757-763
Genomic imprinting is the result of a gamete-specific modification leading to parental origin-specific gene expression in somatic cells of the offspring. Several embryonal tumors show loss of imprinting of genes clustered in human chromosome 11p15.5,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af352392a41d5b3b89eeb738edf9bf1a
https://doi.org/10.1093/hmg/9.5.757
https://doi.org/10.1093/hmg/9.5.757
Autor:
Walter Zumkeller, Stefan Burdach
Publikováno v:
Blood. 94:3653-3657
P ROLIFERATION OF hematopoietic cells is controlled by a coordinated hierarchy of growth factors and their inhibitors. These growth factors form complex signaling networks either by stimulating or inhibiting cell proliferation and differentiation. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3e033546ba8aa4666e716050f16f878
https://doi.org/10.1182/blood.v94.11.3653.423k42_3653_3657
https://doi.org/10.1182/blood.v94.11.3653.423k42_3653_3657
Autor:
Walter Zumkeller, Juerg Schwander, Paul N. Schofield, Chris Mitchell, David J. Morrell, Michael A. Preece
Publikováno v:
European Journal of Cancer. 29:1973-1977
Insulin-like growth factors (IGF)-I, -II and IGF binding protein-2 (IGFBP-2) have been measured in plasma of children with Wilms' tumour. The mean levels for total serum IGF-I and -II were not significantly altered in Wilms' tumour as compared with n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613022befb2735d28a6d41da251bab96
https://doi.org/10.1016/0959-8049(93)90455-o
https://doi.org/10.1016/0959-8049(93)90455-o
Autor:
Paul N. Schofield, Walter Zumkeller
Publikováno v:
Virchows Archiv B Cell Pathology Including Molecular Pathology. 62:207-220
Insulin-like growth factors (IGFs) and their binding proteins are implicated in the growth regulation of the kidney during embryogenesis and differentiation. Recent evidence also suggests that IGFs play a role in kidney physiology (glomerular filtrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b00b91d329f1fcf795e1a2fa424e0c9
https://doi.org/10.1007/bf02899684
https://doi.org/10.1007/bf02899684
Autor:
Walter Zumkeller
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 15:357-369
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6938ed6e4ae0a5b7f9ead8d734f3c3f
https://doi.org/10.1097/00005176-199211000-00001
https://doi.org/10.1097/00005176-199211000-00001
Autor:
Walter, Zumkeller, Marianne, Volleth, Petra, Muschke, Holger, Tönnies, Anita, Heller, Thomas, Liehr, Peter, Wieacker, Markus, Stumm
Publikováno v:
American journal of medical genetics. Part A. (3)
Reports on patients with pure and complete trisomy 12p are rare. Up to now, 12 cases have been described in the literature. Here, we report on the genotype/phenotype-correlation of a female patient with a pure trisomy 12p. Conventional cytogenetic st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7139e56444b35077bd4938199c1dbe0
https://pubmed.ncbi.nlm.nih.gov/15326625
https://pubmed.ncbi.nlm.nih.gov/15326625
Autor:
Markus Stumm, Walter Zumkeller, Albrecht Röpke, Petra Muschke, Hannswerner Gola, Raymonda Varon, Peter Wieacker
Publikováno v:
Prenatal diagnosis. 24(2)
Objective We report on the retrospective diagnosis of Nijmegen breakage syndrome (NBS) confirmed by molecular genetic analysis and consecutive prenatal diagnosis in the same family. Method Thirteen years after the death of their daughter due to fatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fad270e1b6ed9f5ecceb2a24477578d
https://pubmed.ncbi.nlm.nih.gov/14974117
https://pubmed.ncbi.nlm.nih.gov/14974117