Results 271 to 280 of about 9,449,306 (346)
Kinetochore-centrosome feedback linking CENP-E and Aurora kinases controls chromosome congression. [PDF]
Nat CommunVukušić K, Tolić IM.
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Xist in X chromosome inactivation: mechanisms and disease relevance. [PDF]
Cell Commun SignalZhang X +11 more
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Ancestral Chromosome-Level Assemblies Reveal Posthybridization Genome Evolution in the New Mexico Whiptail Lizard (Aspidoscelis neomexicanus). [PDF]
Genome Biol EvolHo DV +11 more
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A comprehensive analysis of the impact of genomic imbalance on gene expression in a poplar aneuploidy population. [PDF]
Commun BiolYu Y +13 more
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Complete de novo assembly and re-annotation of the zebrafish genome
Okendo J +21 more
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Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2008
Fragile sites are heritable specific chromosome loci that exhibit an increased frequency of gaps, poor staining, constrictions or breaks when chromosomes are exposed to partial DNA replication inhibition. They constitute areas of chromatin that fail to compact during mitosis. They are classified as rare or common depending on their frequency within the
T, Lukusa, J P, Fryns
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Fragile sites are heritable specific chromosome loci that exhibit an increased frequency of gaps, poor staining, constrictions or breaks when chromosomes are exposed to partial DNA replication inhibition. They constitute areas of chromatin that fail to compact during mitosis. They are classified as rare or common depending on their frequency within the
T, Lukusa, J P, Fryns
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Current Opinion in Genetics & Development, 1995
The construction of integrated maps at all levels of resolution will facilitate determination of the DNA sequence and, ultimately, the entire gene content of the human genome. In the past two years, the need for extensive frameworks on which to anchor the maps of the human chromosomes has been emphasized. The first framework has been provided following
D R, Bently, I, Dunham
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The construction of integrated maps at all levels of resolution will facilitate determination of the DNA sequence and, ultimately, the entire gene content of the human genome. In the past two years, the need for extensive frameworks on which to anchor the maps of the human chromosomes has been emphasized. The first framework has been provided following
D R, Bently, I, Dunham
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Human Reproduction, 1988
Sperm chromosome studies have been performed in 70 normal males. The incidence of aneuploidy in this group is approximately 3-4%, and that of structural anomalies close to 5%. In carriers of reciprocal or Robertsonian translocations, the results are extremely variable, with percentages of unbalanced sperm from 8 to 87%.
C, Templado +6 more
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Sperm chromosome studies have been performed in 70 normal males. The incidence of aneuploidy in this group is approximately 3-4%, and that of structural anomalies close to 5%. In carriers of reciprocal or Robertsonian translocations, the results are extremely variable, with percentages of unbalanced sperm from 8 to 87%.
C, Templado +6 more
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Archives of Pediatrics & Adolescent Medicine, 1961
The purpose of this paper is to present a nonencyclopedic review of this rapidly growing field. The focus will be on the new methodologies involved, their accomplishments, their limitations, and their potentialities, in the hope of enabling the reader to examine with more understanding the many publications appearing in the clinical literature on the ...
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The purpose of this paper is to present a nonencyclopedic review of this rapidly growing field. The focus will be on the new methodologies involved, their accomplishments, their limitations, and their potentialities, in the hope of enabling the reader to examine with more understanding the many publications appearing in the clinical literature on the ...
openaire +2 more sources