Results 21 to 30 of about 69,824 (308)

Rapid generation of chromosome-specific alphoid DNA probes using the polymerase chain reaction [PDF]

open access: yes, 1992
Non-isotopic in situ hybridization of chromosome-specific alphoid DNA probes has become a potent tool in the study of numerical aberrations of specific human chromosomes at all stages of the cell cycle. In this paper, we describe approaches for the rapid
Dunham, Ian   +7 more
core   +1 more source

Induction of chromosome shattering by ultraviolet light and caffeine: The influence of different distributions of photolesions [PDF]

open access: yes, 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
core   +1 more source

The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study

open access: yesAsian 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
doaj   +1 more source

Quantification of Chromosomal Aberrations in Mammalian Cells

open access: yesBio-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
doaj   +1 more source

Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies [PDF]

open access: yes, 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
core   +1 more source

Prenatal Sonographic Features of Rare Chromosome 13 Aberrations

open access: yesThe 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
doaj  

Identifying Mazama gouazoubira (Artiodactyla; Cervidae) chromosomes involved in rearrangements induced by doxorubicin

open access: yesGenetics 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
doaj   +1 more source

The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary [PDF]

open access: yes, 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
core   +1 more source

Calculating variations in biological effectiveness for a 62 MeV proton beam

open access: yesFrontiers 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
doaj   +1 more source

Multicolour interphase cytogenetics: 24 chromosome probes, 6 colours, 4 layers [PDF]

open access: yes, 2011
From the late 1980s onwards, the use of DNA probes to visualise sequences on individual chromosomes (fluorescent in-situ hybridisation - FISH) revolutionised the study of cytogenetics.
Ellis, Michael   +9 more
core   +1 more source

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