- Coamplification of Multiple Regions of Chromosome 2, Including MYCN, in a Single Patchwork Amplicon in Cancer Cell Lines
[作者:Kitada, K; Aida, S; Aikawa, S,期刊:Cytogenetic and Genome Research, 页码:30-37 , 文章类型: Article,,卷期:2012年136-1]
- Coamplification of multiple segments of chromosome 2, including an MYCN-bearing segment, was examined in 2 cancer cell lines, NCI-H69 (lung cancer) and IMR-32 (neuroblastoma). High-resolution array-CGH analysis revealed ...
- SNP Analysis of Minimally Evolved t(14;18) (q32;q21)-Positive Follicular Lymphomas Reveals a Common Copy-Neutral Loss of Heterozygosity Pattern
[作者:Cheung, KJ; Rogic, S; Ben-Neriah, S; Boyle, M; Connors, JM; Gascoyne, RD; Horsman, DE,期刊:Cytogenetic and Genome Research, 页码:38-43 , 文章类型: Article,,卷期:2012年136-1]
- Follicular lymphoma (FL) cases with a t(14;18)(q32;q21) and minimal or no additional karyotypic alterations, such as copy number gains and losses and/or chromosomal rearrangements, may exhibit pathologic features and a c...
- Molecular Cytogenetic Aberrations in Tunisian Patients with Multiple Myeloma Identified by cIg-FISH in Fixed Bone Marrow Cells
[作者:Gmidene, A; Avet-Loiseau, H; Sennana, H; Ben Abdallah, I; Khlif, A; Meddeb, B; Elloumi, M; Saad, A,期刊:Cytogenetic and Genome Research, 页码:44-49 , 文章类型: Article,,卷期:2012年136-1]
- Cytogenetic studies in multiple myeloma (MM) are hampered by the hypo-proliferative nature of plasma cells. In order to circumvent this problem, we have used a combination of immunolabeling of cytoplasmic Ig light chains...
- Cryptic Introgression of Dasypyrum villosum Parental DNA in Wheat Lines Derived from Intergeneric Hybridization
[作者:Caceres, ME; Pupilli, F; Ceccarelli, M; Vaccino, P; Sarri, V; De Pace, C; Cionini, PG,期刊:Cytogenetic and Genome Research, 页码:75-81 , 文章类型: Article,,卷期:2012年136-1]
- Cytogenetic and DNA molecular analyses have been carried out in 3 wheat introgression lines (ILs; CS x V58, CS x V59, and CS x V60) derived from Triticum aestivum cv. 'Chinese Spring' (CS) x Dasypyrum villosum (Dv) inter...
- A New Case of Pure Partial 7q Duplication
[作者:Alfonsi, M; Palka, C; Morizio, E; Gatta, V; Franchi, S; Franchi, PG; Zori, R; Calabrese, G; Palka, G; Chiarelli, F,期刊:Cytogenetic and Genome Research, 页码:1-5 , 文章类型: Article,,卷期:2012年136-1]
- We report on an 18-month-old boy conceived by assisted reproduction technology with developmental delay, hypotonia, microcephaly, frontal bossing, a mild convergent squint, malformed ears, and a short neck. Karyotype ana...
- Characterizing Small Supernumerary Marker Chromosomes with Combination of Multiple Techniques
[作者:Yu, S; Fiedler, SD; Brawner, SJ; Joyce, JM; Zhou, XG; Liu, HY,期刊:Cytogenetic and Genome Research, 页码:6-14 , 文章类型: Article,,卷期:2012年136-1]
- Fourteen cases with constitutional small supernumerary marker chromosomes (sSMCs) were assessed by combination of diverse techniques including genome-wide high-resolution chromosomal microarray (CMA), chromosome banding ...
- Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
[作者:Vlckova, M; Trkova, M; Zemanova, Z; Hancarova, M; Novotna, D; Raskova, D; Puchmajerova, A; Drabova, J; Zmitkova, Z; Tan, Y; Sedlacek, Z,期刊:Cytogenetic and Genome Research, 页码:15-20 , 文章类型: Article,,卷期:2012年136-1]
- Proximal 6q deletions have a milder phenotype than middle and distal 6q deletions. We describe 2 patients with non-overlapping deletions of about 15 and 19 Mb, respectively, which subdivide the proximal 6q region into 2 ...
- Chromosome Breakage in Human Preimplantation Embryos from Carriers of Structural Chromosomal Abnormalities in Relation to Fragile Sites, Maternal Age, and Poor Sperm Factors
[作者:Xanthopoulou, L; Ghevaria, H; Mantzouratou, A; Serhal, P; Doshi, A; Delhanty, JDA,期刊:Cytogenetic and Genome Research, 页码:21-29 , 文章类型: Article,,卷期:2012年136-1]
- Chromosome breakage is a fairly widespread phenomenon in preimplantation embryos affecting at least 10% of day 3 cleavage stage embryos. It may be detected during preimplantation genetic diagnosis (PGD). For carriers of ...
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