Results 301 to 310 of about 319,606 (332)
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Homologous chromosome recognition via nonspecific interactions

2023
AbstractIn many organisms, most notablyDrosophila, homologous chromosomes in somatic cells associate with each other, a phenomenon known as somatic homolog pairing. Unlike in meiosis, where homology is read out at the level of DNA sequence complementarity, somatic homolog pairing takes place without double strand breaks or strand invasion, thus ...
Wallace F. Marshall, Jennifer C. Fung
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Do homologous chromosomes differ?

Cytogenetic and Genome Research, 1979
This paper is concerned with the problem of deciding whether measurements from homologous chromosomes differ. First, a general mathematical model is proposed for studying the distribution of chromosome measurements. Next, log-likelihood ratios are used to test for correlation between homolog pairs and for differences between homolog means and variances.
D.H. Moore II, A.V. Carrano, B.H. Mayall
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Homologous chromosome pairing

Philosophical Transactions of the Royal Society of London. B, Biological Sciences, 1977
Commonly accepted precepts are challenged : (1) that homologous chromosome pairing is normally mediated by nuclear envelope attachment sites; (2) that crossover site establishment awaits synaptic completion; and (3) that it is the function of the synaptonemal complex to hold homologues in register so that equal crossing over can occur, and perhaps to ...
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Homologous Recombination Using Bacterial Artificial Chromosomes

Cold Spring Harbor Protocols, 2015
This protocol introduces the technique of homologous recombination in bacteria to insert a linear DNA fragment into bacterial artificial chromosomes (BACs). Homologous recombination allows the modification of large DNA molecules, in contrast with conventional restriction endonuclease-based strategies, which cleave large DNAs into numerous fragments and
Cary, Lai   +2 more
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Human chromosome 9 pericentric homologies: implications for chromosome 9 heteromorphisms

Cytogenetic and Genome Research, 1998
Pericentromeric polymorphisms of chromosome 9 include variations in the size of heterochromatin, pericentric inversions, and, more rarely, additional C-band-negative, G-band-positive material in either the proximal short arm or long arm or within the heterochromatin.
J P, Park   +4 more
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Chimpanzee chromosome 12 is homologous to human chromosome arm 2q

Cytogenetic and Genome Research, 1978
Most of the 46 human chromosomes find their counterparts in the 48 chimpanzee chromosomes except for chromosome 2 which has been hypothesized to have been derived from a centric fusion of two chimpanzee acrocentric chromosomes. These two chromosomes correspond to the human chromosomes 2p and 2g.
N C, Sun, C R, Sun, T, Ho
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Chromosomal homology in southern Akodon

Experientia, 1982
Differential staining (G and C) of southern South American Akodon are presented. A. olivaceus, A. longipilis and A. sanborni all have the same karyotype (2n = 52, NF = 58). A virtually identical band sequence is observed. This situation is interpreted using the canalization model of chromosomal evolution which stresses an optimum karyotype for each ...
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Do homologous chromosomes differ?

Cytogenetic and Genome Research, 1973
Two statistics are derived for testing whether measurements on otherwise indistinguishable chromosome pairs differ. The power of these tests is shown as well as a method for estimating the true homolog means. The tests and estimation procedures are simple to compute, and their use is illustrated on chromosome data.
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Chromosome ends initiate homologous chromosome pairing during rice meiosis

Plant Physiology
Abstract During meiotic prophase I, chromosomes undergo large-scale dynamics to allow homologous chromosome pairing, prior to which chromosome ends attach to the inner nuclear envelope and form a chromosomal bouquet. Chromosome pairing is crucial for homologous recombination and accurate chromosome segregation during meiosis.
Hanli You   +11 more
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Homologous Association of Oppositely Imprinted Chromosomal Domains

Science, 1996
Human chromosome 15q11-q13 encompasses the Prader-Willi syndrome (PWS) and the Angelman syndrome (AS) loci, which are subject to parental imprinting, a process that marks the parental origin of certain chromosomal subregions. A temporal and spatial association between maternal and paternal chromosomes 15 was observed in human T lymphocytes by three ...
J M, LaSalle, M, Lalande
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