Results 1 to 10 of about 63,041 (164)

An intelligent recognition method of chromosome rearrangement patterns based on information entropy [PDF]

open access: yesScientific Reports, 2022
Chromosome rearrangements play an important role in the speciation of plants and animals, and the recognition of chromosome rearrangement patterns is helpful to elucidate the mechanism of species differentiation at the chromosome level.
Fushun Wang   +6 more
doaj   +2 more sources

Engineering chromosome rearrangements in cancer [PDF]

open access: yesDisease Models & Mechanisms, 2021
ABSTRACT The identification of large chromosomal rearrangements in cancers has multiplied exponentially over the last decade. These complex and often rare genomic events have traditionally been challenging to study, in part owing to lack of tools that efficiently engineer disease-associated inversions, deletions and translocations in ...
Salvador Alonso, Lukas E. Dow
openaire   +3 more sources

Complex X chromosome rearrangement associated with multiorgan autoimmunity [PDF]

open access: yesMolecular Cytogenetics, 2015
Artur Beke   +2 more
exaly   +2 more sources

Conserved Patterns of Symmetric Inversion in the Genome Evolution of Bordetella Respiratory Pathogens

open access: yesmSystems, 2019
Whooping cough (pertussis), primarily caused by Bordetella pertussis, has resurged in the United States, and circulating strains exhibit considerable chromosome structural fluidity in the form of rearrangement and deletion.
Michael R. Weigand   +14 more
doaj   +3 more sources

Gross Chromosomal Rearrangement at Centromeres

open access: yesBiomolecules, 2023
Centromeres play essential roles in the faithful segregation of chromosomes. CENP-A, the centromere-specific histone H3 variant, and heterochromatin characterized by di- or tri-methylation of histone H3 9th lysine (H3K9) are the hallmarks of centromere chromatin.
Ran Xu, Ziyi Pan, Takuro Nakagawa
openaire   +3 more sources

Dynamics of the compartmentalized Streptomyces chromosome during metabolic differentiation

open access: yesNature Communications, 2021
Streptomyces bacteria have a linear chromosome, with core genes located in the central region and gene clusters for specialized metabolite biosynthesis found in the ‘arms’. Here, Lioy et al.
Virginia S. Lioy   +17 more
doaj   +1 more source

Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature [PDF]

open access: yesInternational Journal of Fertility and Sterility, 2016
Chromosomal defects are relatively frequent in infertile men however, translocations between the Y chromosome and autosomes are rare and less than 40 cases of Y-autosome translocation have been reported.
Alfredo Orrico   +7 more
doaj   +1 more source

Chromosome Rearrangements in Canine Fibrosarcomas [PDF]

open access: yesJournal of Heredity, 2005
We have previously reported the use of six- and seven-color paint sets in the analysis of canine soft tissue sarcomas. Here we combine this technique with flow sorting of translocation chromosomes, reverse painting, and polymerase chain reaction (PCR) analysis of the gene content of the reverse paint in order to provide a more detailed analysis of ...
D R, Sargan   +6 more
openaire   +2 more sources

A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning

open access: yesMolecular Cytogenetics, 2017
Background Neocentromeres are rare and considered chromosomal aberrations, because a non-centromeric region evolves in an active centromere by mutation.
N. Villa   +7 more
doaj   +1 more source

Aberrant X chromosomal rearrangement through multi‐step template switching during sister chromatid formation in a patient with severe hemophilia A

open access: yesMolecular Genetics & Genomic Medicine, 2020
Background Hemophilia A (HA) is an X‐linked recessive bleeding disorder caused by pathogenic variants of the coagulation factor VIII gene (F8). Half of the patients with severe HA have a recurrent inversion in the X chromosome, that is, F8 intron 22 or ...
Mahiru Tokoro   +14 more
doaj   +1 more source

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