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Keywords: Chromosome
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Journal Articles
Journal Articles
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2021) 161 (3-4): 120–131.
Published Online: 21 July 2021
...Xueluo Zhang; Junmei Fan; Yanhua Chen; Jun Wang; Zhijiao Song; Jinghui Zhao; Zhongyun Li; Xueqing Wu; Yuanjing Hu In the present study, we retrospectively recruited 340 patients who underwent spontaneous abortions to investigate chromosomal abnormalities of the conception products in the first...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2021) 161 (1-2): 82–92.
Published Online: 17 February 2021
...(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Array CGH Chromosome Melanoma Multicolor FISH Murine tumor cell lines Translocations Skin cancer is one...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2020) 160 (11-12): 698–703.
Published Online: 18 November 2020
...Ross Brookwell; Kimberly Finlayson; Jason P. van de Merwe The karyotype of the Odontocete whale, Mesoplodon densirostris , has not been previously reported. The chromosome number is determined to be 2n = 42, and the karyotype is presented using G-, C-, and nucleolar organizer region (NOR) banding...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2017) 151 (3): 161–170.
Published Online: 24 March 2017
... respectively labeled with TAMRA or digoxigenin to hybridize with mitotic chromosomes for samples of all localities. It turned out that all probes showed the same signals that appeared in every centromeric region and in the telomeric regions of chromosome 5, without differences within or between populations...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2014) 142 (4): 245–248.
Published Online: 09 May 2014
... microscopy showed a cellular spindle cell tumor composed of oval to spindly cells arranged in sheets or fascicles supported by a rich vascular network and stained positive for smooth muscle markers (SMA, HHF35). The majority of metaphase cells from the short-term cultures of tumor cells had 49 chromosomes...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2013) 140 (2-4): 226–240.
Published Online: 08 July 2013
..., androgenetic) animals can be compared. First, we summarize the chromosome manipulation techniques to induce triploids and tetraploids by inhibiting meiotic or mitotic divisions of inseminated eggs, respectively, as well as parthenogenetic animals, obtained after fertilization with genetically inactivated...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2013) 140 (1): 62–69.
Published Online: 26 April 2013
...A.E. Barros e Silva; W. dos Santos Soares Filho; M. Guerra Sites of 5S and 45S rDNA are more commonly located on different chromosomes of most angiosperms. Previous investigations have shown that in the subfamily Aurantioideae these sites may appear closely linked (adjacent sites...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2012) 136 (3): 220–228.
Published Online: 18 February 2012
...H. Xu; D. Yin; L. Li; Q. Wang; X. Li; X. Yang; W. Liu; D. An To develop a set of molecular markers specific for the chromosome arms of rye, a total of 1,098 and 93 primer pairs derived from the expressed sequence tag (EST) sequences distributed on all 21 wheat chromosomes and 7 rye chromosomes...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2011) 133 (2-4): 107–118.
Published Online: 28 January 2011
...E. Fragouli; D. Wells; J.D.A. Delhanty Aneuploidy is the most commonly occurring type of chromosome abnormality and the most significant clinically. It arises mostly due to segregation errors taking place during female meiosis and is also closely associated with advancing maternal age. Two main...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2011) 133 (2-4): 149–159.
Published Online: 19 January 2011
...E. Fragouli; D. Wells Studies of human cleavage stage embryos, 3 days after fertilization of the oocyte, have revealed remarkably high levels of chromosome abnormality. In addition to meiotic errors derived from the gametes, principally the oocyte, mitotic errors occurring after fertilization...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2011) 133 (2-4): 280–291.
Published Online: 06 January 2011
... hours however, although convincing studies suggesting an age effect for disomies 1, 9, 18 and 21 and the sex chromosomes are in the literature, others failed to notice any association for these or other chromosomes. It is biologically plausible that chromosomal non-disjunction errors should increase...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2011) 133 (2-4): 269–279.
Published Online: 19 November 2010
...D. Ioannou; D.K. Griffin Numerous studies have implicated the role of gross genomic rearrangements in male infertility, e.g., constitutional aneuploidy, translocations, inversions, Y chromosome deletions, elevated sperm disomy, and DNA damage. The primary purpose of this paper is to review male...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2010) 129 (1-3): 55–63.
Published Online: 13 July 2010
...T. Wako; K. Fukui Plants have a wide range of genome sizes. The length of each DNA molecule is usually much longer than the diameter of the cell and the length of each metaphase chromosome is effectively shortened to progress through mitosis. Thus some questions arise, such as: How is genomic DNA...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2010) 129 (1-3): 211–223.
Published Online: 26 May 2010
... complexity can, however, be reduced by using flow cytometry to isolate individual chromosomes, and these can be exploited to construct chromosome-specific BAC libraries. Such libraries simplify the task of physical map construction, positional cloning and the targeted development of genetic markers. Rapid...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2010) 129 (1-3): 234–240.
Published Online: 22 May 2010
...O. Riera-Lizarazu; J.M. Leonard; V.K. Tiwari; S.F. Kianian Radiation hybrid (RH) mapping is based on radiation-induced chromosome breakage rather than meiotic recombination, as a means to induce marker segregation for mapping. To date, the implementation of this mapping approach in hexaploid...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2009) 127 (2-4): 273–279.
Published Online: 25 March 2010
... species exhibited many chromosome aberrations which were associated with their complete or partial sterility. In addition, the karyotype and the structure of mitotic and meiotic lampbrush chromosomes in 2 species and in some back-cross hybrids of this unisexual-bisexual complex have been examined here...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2009) 127 (1): 33–42.
Published Online: 29 January 2010
... was absent in all the other tested archaeo- and neo-bratrachian species, as well as non-amphibian species. Fluorescent in situ hybridization (FISH) analysis shows that Dp-sat1 is localized only in peri- and/or para-centromeric areas of the 7 small chromosome pairs, while no labeling was observed in the 7...
Journal Articles
Subject Area:
Genetics
Cytogenet Genome Res (2009) 125 (2): 162–164.
Published Online: 31 August 2009
... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Chromosome Idiogram ISCN Level of resolution Short Communication Cytogenet Genome Res 2009;125:162 164 DOI: 10.1159/000227842 Accepted after revision: March 6, 2009...