Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Markus Eckart"'
Autor:
Barbara J. Lamb, Rork Kuick, Peter F. Ambros, Markus Eckart, Andreas Weinhäusl, Xiao-Xiang Zhu, Katharina Wimmer, Jean Marie Rouillard, Christa Fonatsch, Sam M. Hanash
Publikováno v:
Genes, Chromosomes and Cancer. 33:285-294
Restriction landmark genome scanning (RLGS) allows comparative analysis of several thousand DNA fragments in the genome and provides a means to identify CpG islands that are altered in tumor cells as a result of amplification, deletion, or methylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96bb6b831081f003d379c2a0f18ee6af
https://doi.org/10.1002/gcc.10030
https://doi.org/10.1002/gcc.10030
Publikováno v:
Human Genetics. 106:311-313
Neurofibromatosis type 1 (NF1) is a common inherited disease affecting one in 3,500 individuals. The mutation rate in the NF1 gene is one of the highest known for human genes. Compared to other methods, the protein truncation test (PTT) and subsequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::834163c194836065a5dc862a6f0118ab
https://doi.org/10.1007/s004390051043
https://doi.org/10.1007/s004390051043
Autor:
Nitzschke, Markus Eckart.
Thesis (doctoral)--Albert-Ludwigs-Universität Freiburg im Breisgau, 2006.
Autor:
Katharina Wimmer, Torsten Pietsch, Jean Marie Rouillard, Wolfgang Hartmann, Andrea Zatkova, Arend Koch, Dietrich von Schweinitz, Christa Fonatsch, Sam M. Hanash, Barbara J. Lamb, Markus Eckart, Rork Kuick
Publikováno v:
Genes, chromosomescancer. 39(2)
There is evidence that 8q amplification is associated with poor prognosis in hepatoblastoma. A previous comparative genomic hybridization analysis identified a critical region in chromosomal bands 8q11.2-q13. Using restriction landmark genomic scanni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e038c5486e014625ad92ad036d1bc7c
https://pubmed.ncbi.nlm.nih.gov/14695992
https://pubmed.ncbi.nlm.nih.gov/14695992
Publikováno v:
Journal of neuropathology and experimental neurology. 61(10)
Children with neurofibromatosis type I (NF1) have a highly increased risk for developing optic nerve gliomas. Several lines of evidence support the notion that the NF1 gene functions as tumor suppressor in these pilocytic astrocytomas and therefore i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdaa1125ec5564071b2f653f56681e4f
https://pubmed.ncbi.nlm.nih.gov/12387455
https://pubmed.ncbi.nlm.nih.gov/12387455
Autor:
Katharina, Wimmer, Xiao-xiang, Zhu Xx, Jean Marie, Rouillard, Peter F, Ambros, Barbara J, Lamb, Rork, Kuick, Markus, Eckart, Andreas, Weinhäusl, Christa, Fonatsch, Sam M, Hanash
Publikováno v:
Genes, chromosomescancer. 33(3)
Restriction landmark genome scanning (RLGS) allows comparative analysis of several thousand DNA fragments in the genome and provides a means to identify CpG islands that are altered in tumor cells as a result of amplification, deletion, or methylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c48daa1bd3b1097d88b0f0f543de574
https://pubmed.ncbi.nlm.nih.gov/11807986
https://pubmed.ncbi.nlm.nih.gov/11807986
Autor:
Markus Eckart, Katharina Wimmer, Ludwine Messiaen, Tom Callens, Thomas Birkner, Helga Rehder, Christa Fonatsch, Manfred Mühlbauer, Jules G. Leroy
Publikováno v:
European journal of human genetics : EJHG. 10(5)
Spinal neurofibromas are found in up to 38% of NF1 patients. However, they cause clinical implications only in about 5% of the patients. In contrast, multiple symptomatic spinal neurofibromas are the main clinical finding in patients with familial sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68a7d93aaf7e6bf71910f88bb4cb7fa
https://pubmed.ncbi.nlm.nih.gov/12082509
https://pubmed.ncbi.nlm.nih.gov/12082509
Publikováno v:
Scopus-Elsevier
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting one in 3,500 individuals. The mutation rate in the NF1 gene is one of the highest known for human genes. Compared to other methods, the protein truncation test (PTT) p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b72984e93c93d652b958f991bacfc04f
https://pubmed.ncbi.nlm.nih.gov/10874316
https://pubmed.ncbi.nlm.nih.gov/10874316
Publikováno v:
Human Mutation. 16:90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52da9aefef442b0a4d1d2c62a08ef654
https://doi.org/10.1002/1098-1004(200007)16:1<90::aid-humu20>3.3.co
https://doi.org/10.1002/1098-1004(200007)16:1<90::aid-humu20>3.3.co
Autor:
Andrea Zatkova, Jean-Marie Rouillard, Wolfgang Hartmann, Barbara J. Lamb, Rork Kuick, Markus Eckart, Dietrich von Schweinitz, Arend Koch, Christa Fonatsch, Torsten Pietsch, Sam M. Hanash, Katharina Wimmer
Publikováno v:
Genes, Chromosomes & Cancer; Feb2004, Vol. 39 Issue 2, p126-137, 12p