Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anja Matthaei"'
Autor:
Sigrid Tinschert, W. Werner, Anja Matthaei, Konrad Oexle, Klaus G. Hinkel, Oliver Bartsch, Inna Nitz, Andreas Rump, Evelin Schröck, Eva-Maria Gerlach, Ulrike Koerner, Alexander Herr
Publikováno v:
European Journal of Medical Genetics. 48:328-338
A 5.4-year-old male propositus is reported with mild dysmorphic features including hypoplasia of the radial part of both hands affecting thenar, thumb and fingers 2-3, incomplete syndactyly of fingers 3-4, single palmar creases, brachymesophalangia o
Autor:
Beatriz Carvalho, Michael Vieth, Catia Moutinho, Gerrit A. Meijer, Manfred Stolte, Anja Matthaei, Fátima Carneiro, Tineke E. Buffart, Rui Manuel Reis, Nicole C.T. van Grieken, Cornelis J.H. van de Velde, Paula Silva, Evelin Schröck, Thomas Mons, Bauke Ylstra
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Buffart, T E, Carvalho, B, Mons, T, Reis, R M, Moutinho, C, Silva, P, van Grieken, N C T, Vieth, M, Stolte, M, van de Velde, C J H, Schrock, E, Matthaei, A, Ylstra, B, Carneiro, F & Meijer, G A 2007, ' DNA copy number profiles of gastric cancer precursor lesions ', BMC Genomics, vol. 8, 345 . https://doi.org/10.1186/1471-2164-8-345
BMC Genomics, Vol 8, Iss 1, p 345 (2007)
BMC Genomics, 8:345. BioMed Central
BMC Genomics
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Buffart, T E, Carvalho, B, Mons, T, Reis, R M, Moutinho, C, Silva, P, van Grieken, N C T, Vieth, M, Stolte, M, van de Velde, C J H, Schrock, E, Matthaei, A, Ylstra, B, Carneiro, F & Meijer, G A 2007, ' DNA copy number profiles of gastric cancer precursor lesions ', BMC Genomics, vol. 8, 345 . https://doi.org/10.1186/1471-2164-8-345
BMC Genomics, Vol 8, Iss 1, p 345 (2007)
BMC Genomics, 8:345. BioMed Central
BMC Genomics
Chromosomal instability (CIN) is the most prevalent type of genomic instability in gastric tumours, but its role in malignant transformation of the gastric mucosa is still obscure. In the present study, we set out to study whether two morphologically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ac4b8ab6bf62165803d8f43d8f8d7e
Autor:
Anja Matthaei, Thomas Heiden, Klaus Hermann, Evelin Schröck, Anne Helmrich, Karen Stout-Weider
Publikováno v:
International journal of cancer. 120(1)
Common fragile sites (CFSs) are expressed as chromosome gaps in cells of different species including human and mouse as a result of the inhibition of DNA replication. They may serve as hot spots for DNA breakage in processes such as tumorigenesis and
Autor:
P. Zschieschang, Evelin Schröck, Anne Helmrich, Karen Stout-Weider, Anja Matthaei, Tanja Hardt, Peter O’Brien
Publikováno v:
Cytogenet Genome Res 114:199–221(2006), ISSN: 1424-8581
Spectral karyotyping (SKY) is a widely used methodology to identify genetic aberrations. Multicolor fluorescence in situ hybridization using chromosome painting probes in individual colors for all metaphase chromosomes at once is combined with a uniq
Autor:
Evelin Schröck, Robert Grützmann, Christian Pilarsky, Anja Matthaei, Andreas Rump, Juliane Artelt, Alexander Herr
Publikováno v:
Genomics. 85(3)
Array-based comparative genome hybridization is a powerful tool for detecting chromosomal imbalances at high resolution. However, the design and setup of such arrays are time consuming and expensive and thus worthwhile only when large numbers of arra