Prenatal Sonographic Features of Rare Chromosome 13 Aberrations
The Application of Clinical Genetics, 2022 Hanna Moczulska,1 Michal Pietrusinski,1 Marcin Serafin,1 Beata Skoczylas,1 Piotr Sieroszewski,2 Maciej Borowiec1 1Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland; 2Department of Fetal Medicine and Gynecology, Medical University ...
Moczulska H +5 more
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Genetics and Molecular Biology, 2017 The process of karyotype evolution in Cervidae from a common ancestor (2n = 70, FN = 70) has been marked by complex chromosomal rearrangements. This ancestral karyotype has been retained by the current species Mazama gouazoubira (Fischer 1814), for which
Iara Maluf Tomazella +2 more
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Asian Journal of Andrology, 2020 Chromosomal abnormalities and Y chromosome microdeletions are considered to be the two more common genetic causes of spermatogenic failure. However, the relationship between chromosomal aberrations and Y chromosome microdeletions is still unclear.
Hong-Ge Li +6 more
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Quantification of Chromosomal Aberrations in Mammalian Cells
Bio-Protocol, 2023 Maintenance of genome integrity requires efficient and faithful resolution of DNA breaks and DNA replication obstacles. Dysfunctions in any of the processes orchestrating such resolution can lead to chromosomal instability, which appears as numerical and
Inés Paniagua, Jacqueline Jacobs
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Induction of chromosome shattering by ultraviolet light and caffeine: The influence of different distributions of photolesions [PDF]
, 1986 Cells of synchonized and of asynchronously growing cultures of a V79 Chinese hamster line were microirradiated with a low poweer laser-UV-microbeam of wavelength 257 nm.
Cremer, Thomas, Cremer, Christoph
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Calculating variations in biological effectiveness for a 62 MeV proton beam
Frontiers in Oncology, 2016 A biophysical model of radiation-induced cell death and chromosome aberrations (called BIANCA, BIophysical ANalysis of Cell death and chromosome Aberrations) was further developed and applied to therapeutic protons.
Mario Pietro Carante +3 more
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Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies [PDF]
, 1992 Chromosomal in situ suppression (CISS) hybridization was performed with library DNA from sorted human chromosomes 8, 9, 15, 17, 21, and 22 on immunologically stained bone marrow cells of four patients with a hematologic neoplasm, including two patients ...
Knuutila, Sakari +15 more
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Metaphase and Interphase Cytogenetics with Alu-PCR-amplified Yeast Artificial Chromosome Clones Containing the BCR Gene and the Protooncogenes c-raf-1, c-fms, and c-erbB-21 [PDF]
, 1992 A human yeast artificial chromosome (YAC) library was screened by polymerase chain reaction with oligonucleotide primers defined for DNA sequences of the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erB-2.
Olson, Maynard V. +8 more
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Clinical cytogenetics in river buffalo
Italian Journal of Animal Science, 2011 While autosomal numeric chromosome abnormalities are phenotipically visible (abnormal body conformation) and easily eliminated during the normal breeding selection, sex numeric abnormalities (including the cases of free-martinism), as well as the ...
L. Zicarelli +3 more
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The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary [PDF]
, 1994 Fluorescencein situ hybridization (FISH) of microlibraries established from distinct chromosome subregions can test the evolutionary conservation of chromosome bands as well as chromosomal rearrangements that occurred during primate evolution and will ...
Cremer, Thomas +8 more
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