نتایج جستجو برای: multiple chromosomal changes

تعداد نتایج: 1613428  

2012
Allen Edward Coleman Nicole McNeil Alexander Leonidovich Kovalchuck Dara Wangsa Thomas Ried Hong Wang

Anesthesia is widely used in several medical settings and accepted as safe. However, there is some evidence that anesthetic agents can induce genomic changes leading to neural degeneration or apoptosis. Although chromosomal changes have not been observed in vivo, this is most likely due to DNA repair mechanisms, apoptosis, or cellular senescence. Potential chromosomal alterations after exposure...

2018
J. W. Venema G. Kok Jan Leenhouts K. Leenhouts

An integration vector, pORI13, was developed to screen in Lactococcus lactis for expression signals induced by changes in the environment and to assay transcriptional activity of genes in single copy. The plasmid carries a promoterless Escherichia coli lacZ gene preceded by a start codon, a lactococcal ribosome binding site, and a multiple cloning site. Chromosomal Sau3AI fragments of L. lactis...

Journal: :Genetics 1998
B S Strauss

The presence of numerous chromosomal changes and point mutations in tumors is well established. At least some of these changes play a role in the development of the tumors. It has been suggested that the number of these genetic changes requires that tumorigenesis involves an increase in mutation rate. However, the presence of numerous changes can also be accounted for by efficient selection. Wh...

Journal: :Cancer research 1995
K M Fong P V Zimmerman P J Smith

Microsatellites are highly polymorphic, short-tandem repeat sequences dispersed throughout the genome. Instability of these repeat sequences at multiple genetic loci may result from mismatch repair errors and occur in hereditary nonpolyposis colorectal carcinoma and certain sporadic cancers. In non-small cell lung cancer, we found that microsatellite instability was infrequent, affecting only 7...

2006
Kwun M. Fong Paul V. Zimmerman Peter J. Smith

Microsatellites are highly polymorphic, short-tandem repeat sequences dispersed throughout the genome. Instability of these repeat sequences at multiple genetic loci may result from mismatch repair errors and occur in hereditary nonpolyposis colorectal carcinoma and certain sporadic can cers. In non-small cell lung cancer, we found that microsatellite instability was infrequent, affecting only ...

Journal: :Molecular biology and evolution 2001
C H Slamovits J A Cook E P Lessa M S Rossi

We investigated the relationship between satellite copy number and chromosomal evolution in tuco-tucos (genus Ctenomys), a karyotypically diverse clade of rodents. To explore phylogenetic relationships among 23 species and 5 undescribed forms, we sequenced the complete mitochondrial cytochrome b genes of 27 specimens and incorporated 27 previously published sequences. We then used quantitative ...

Journal: :Arquivos De Neuro-psiquiatria 2023

Case presentation: Comparative genomic hybridization based on microarrays (array CGH) is a reality in clinical practice the neuropediatric population. It allows high-resolution assessment of DNA copy number changes associated with chromosomal abnormalities. Objective: To highlight importance using technique investigation patients diverse phenotypes. Methods: Series case studies.

2017
K. Leenhouts

An integration vector, pORI13, was developed to screen in Lactococcus lactis for expression signals induced by changes in the environment and to assay transcriptional activity of genes in single copy. The plasmid carries a promoterless Escherichia coli lacZ gene preceded by a start codon, a lactococcal ribosome binding site, and a multiple cloning site. Chromosomal Sau3AI fragments of L. lactis...

Journal: :Bioinformatics 2004
Chad L. Myers Maitreya J. Dunham Sun-Yuan Kung Olga G. Troyanskaya

MOTIVATION Chromosomal copy number changes (aneuploidies) are common in cell populations that undergo multiple cell divisions including yeast strains, cell lines and tumor cells. Identification of aneuploidies is critical in evolutionary studies, where changes in copy number serve an adaptive purpose, as well as in cancer studies, where amplifications and deletions of chromosomal regions have b...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Michael Chester Joseph P Gallagher V Vaughan Symonds Ana Veruska Cruz da Silva Evgeny V Mavrodiev Andrew R Leitch Pamela S Soltis Douglas E Soltis

Polyploidy, or whole genome duplication, has played a major role in the evolution of many eukaryotic lineages. Although the prevalence of polyploidy in plants is well documented, the molecular and cytological consequences are understood largely from newly formed polyploids (neopolyploids) that have been grown experimentally. Classical cytological and molecular cytogenetic studies both have show...

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