- Sequence based high resolution chromosomal CGH
[作者：Kowalska, A; Brunner, B; Bozsaky, E; Chen, QR; Stock, C; Lorch, T; Khan, J; Ambros, PF,期刊：Cytogenetic and Genome Research, 页码：1-6 , 文章类型： Article，,卷期：2008年121-1]
- We aimed to directly align a chromosomal CGH (cCGH) pattern with the gene mapping data by taking advantage of the clustering of the GGCC motif at certain positions in the human genome. The alignment of chromosomal with s...
- An improved method for generating BAC DNA suitable for FISH
[作者：Roohi, J; Cammer, M; Montagna, C; Hatchwell, E,期刊：Cytogenetic and Genome Research, 页码：7-9 , 文章类型： Article，,卷期：2008年121-1]
- Fluorescence in situ hybridization ( FISH) is commonly used to identify chromosomal aberrations such as translocations, deletions, duplications, gene fusions, and aneuploidies. It relies on the hybridization of fluoresce...
- Microarray mRNA expression analysis of Fanconi anemia fibroblasts
[作者：Galetzka, D; Weis, E; Rittner, G; Schindler, D; Haaf, T,期刊：Cytogenetic and Genome Research, 页码：10-13 , 文章类型： Article，,卷期：2008年121-1]
- Fanconi anemia ( FA) cells are generally hypersensitive to DNA cross-linking agents, implying that mutations in the different FANC genes cause a similar DNA repair defect(s). By using a customized cDNA microarray chip fo...
- Characterization of a familial small supernumerary marker chromosome in a patient with adult-onset tongue cancer
[作者：Bakshi, SR; Dave, BJ; Sanger, W; Brahmbhatt, MM; Trivedi, PJ; Kakadia, PM; Patel, SJ,期刊：Cytogenetic and Genome Research, 页码：14-17 , 文章类型： Article，,卷期：2008年121-1]
- Cytogenetic analysis in peripheral blood lymphocytes of a 50-year-old female with tongue cancer showed the presence of one to three copies of a small supernumerary marker chromosome (sSMC) in a mosaic state. Family studi...
- Karyotype analysis of the euploid cell population of a mouse embryonic stem cell line revealed a high incidence of chromosome abnormalities that varied during culture
[作者：Rebuzzini, P; Neri, T; Mazzini, G; Zuccotti, M; Redi, CA; Garagna, S,期刊：Cytogenetic and Genome Research, 页码：18-24 , 文章类型： Article，,卷期：2008年121-1]
- It is common knowledge that mouse embryonic stem cell (mESC) lines accumulate chromosomal changes during culture. Despite the wide use of mESCs as a model of early mammalian development and cell differentiation, there is...
- Cytogenetic studies and karyotype nomenclature of three wild canid species: maned wolf (Chrysocyon brachyurus), bat-eared fox (Otocyon megalotis) and fennec fox (Fennecus zerda)
[作者：Pienkowska-Schelling, A; Schelling, C; Zawada, M; Yang, F; Bugno, M; Ferguson-Smith, M,期刊：Cytogenetic and Genome Research, 页码：25-34 , 文章类型： Article，,卷期：2008年121-1]
- We have analysed the chromosomes of three wild and endangered canid species: the maned wolf (Chrysocyon brachyurus), the bat-eared fox (Otocyon megalotis) and the fennec fox (Fennecus zerda) using classical and molecular...
- A comparative radiation hybrid map of sheep chromosome 10
[作者：Drogemuller, M; Tetens, J; Dalrymple, B; Goldammer, T; Wu, CH; Cockett, NE; Leeb, T; Drogemuller, C,期刊：Cytogenetic and Genome Research, 页码：35-40 , 文章类型： Article，,卷期：2008年121-1]
- Comparative radiation hybrid (RH) maps of individual ovine chromosomes are essential to identify genes governing traits of economic importance in sheep, a livestock species for which whole genome sequence data are not ye...
- Genomic organization, expression and evolution of porcine CRSP1, 2, and 3
[作者：Rezaeian, AH; Katafuchi, T; Yoshizawa, M; Hiraiwa, N; Saito, T; Nishibori, M; Hamano, K; Minamino, N; Yasue, H,期刊：Cytogenetic and Genome Research, 页码：41-49 , 文章类型： Article，,卷期：2008年121-1]
- Recently we identified and characterized porcine calcitonin receptor-stimulating peptide (CRSP) 1, CRSP2 and CRSP3 as members of the calcitonin/calcitonin gene-related peptide (CT/CGRP) family. In the present study, the ...
- Non-homologous sex chromosomes in two species of the genus Eigenmannia (Teleostei : Gymnotiformes)
[作者：Henning, F; Trifonov, V; Ferguson-Smith, MA; de Almeida-Toledo, LF,期刊：Cytogenetic and Genome Research, 页码：55-58 , 文章类型： Article，,卷期：2008年121-1]
- The Neotropical genus Eigenmannia is a fish group with unknown species diversity where representatives possess a broad range of chromosomal sex determining systems namely XY/XX, X1X2Y/X1X1X2X2, ZZ/ZW as well as homomorph...
- Down syndrome and the genes of human chromosome 21: current knowledge and future potentials
[作者：Pritchard, M; Reeves, RH; Dierssen, M; Patterson, D; Gardiner, KJ,期刊：Cytogenetic and Genome Research, 页码：67-77 , 文章类型： Article，,卷期：2008年121-1]
- Down syndrome (DS), trisomy of human chromosome 21, is the most common genetic cause of intellectual disability. With an incidence in some countries as high as one in approximately 700 live births, and a complex, extensi...
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