Results 41 to 50 of about 769,627 (258)

Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12

open access: yesGenomics, 1997
A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers.
Sun, H.S.   +12 more
openaire   +5 more sources

Transcriptional network analysis of PTEN‐protein‐deficient prostate tumors reveals robust stromal reprogramming and signs of senescent paracrine communication

open access: yesMolecular Oncology, EarlyView.
Combining PTEN protein assessment and transcriptomic profiling of prostate tumors, we uncovered a network enriched in senescence and extracellular matrix (ECM) programs associated with PTEN loss and conserved in a mouse model. We show that PTEN‐deficient cells trigger paracrine remodeling of the surrounding stroma and this information could help ...
Ivana Rondon‐Lorefice   +16 more
wiley   +1 more source

Genome-wide linkage scan for factors of metabolic syndrome in a Chinese population

open access: yesBMC Genetics, 2010
Background Shared genetic factors may contribute to the phenotypic clustering of different components of the metabolic syndrome (MES). This study aims to identify genetic loci that contribute to individual or multiple factors related to MES.
Chan Juliana CN   +5 more
doaj   +1 more source

Cytogenetic study of two Solenanthus Ledeb. species (Boraginaceae) in Iran [PDF]

open access: yesJournal of Cell and Molecular Research, 2013
Chromosome number, meiotic behavior, and pollen viability were analyzed in 2 species of genus Solenanthus, S. stamineus (Desf.) Wettst. and S. circinnatus Ledeb, from Iran. This report is the first cytogenetic analysis of these species.
Massoud Ranjbar   +2 more
doaj   +1 more source

Phenotypic and genotypic characterization of single circulating tumor cells in the follow‐up of high‐grade serous ovarian cancer

open access: yesMolecular Oncology, EarlyView.
Single circulating tumor cells (sCTCs) from high‐grade serous ovarian cancer patients were enriched, imaged, and genomically profiled using WGA and NGS at different time points during treatment. sCTCs revealed enrichment of alterations in Chromosomes 2, 7, and 12 as well as persistent or emerging oncogenic CNAs, supporting sCTC identity.
Carolin Salmon   +9 more
wiley   +1 more source

Molecular Detection of Genes Related to Antimicrobial Resistance harbored on chromosome by PCR assay in P. aeruginosa [PDF]

open access: yesBasrah Journal of Veterinary Research
Forty-two typical P. aeruginosa strains were chosen, and Eight antibiotic-resistance genes linked to a spontaneous outbreak of the bacteria were analyzed (the same strains that were tested for the antimicrobial susceptibility). The findings revealed that
Tamadhar Al-tememe, Basil Abbas
doaj   +1 more source

Tumour–host interactions in Drosophila: mechanisms in the tumour micro‐ and macroenvironment

open access: yesMolecular Oncology, EarlyView.
This review examines how tumour–host crosstalk takes place at multiple levels of biological organisation, from local cell competition and immune crosstalk to organism‐wide metabolic and physiological collapse. Here, we integrate findings from Drosophila melanogaster studies that reveal conserved mechanisms through which tumours hijack host systems to ...
José Teles‐Reis, Tor Erik Rusten
wiley   +1 more source

Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array. [PDF]

open access: yesPLoS ONE, 2015
Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) is an autosomal recessive disease caused by biallelic mutations in the vitamin D receptor (VDR) gene.
Mayuko Tamura   +10 more
doaj   +1 more source

Subtype‐specific enhancer RNAs define transcriptional regulators and prognosis in breast cancers

open access: yesMolecular Oncology, EarlyView.
This study employed machine learning methodologies to perform the subtype‐specific classification of RNA‐seq data sets, which are mapped on enhancers from TCGA‐derived breast cancer patients. Their integration with gene expression (referred to as ProxCReAM eRNAs) and chromatin accessibility profiles has the potential to identify lineage‐specific and ...
Aamena Y. Patel   +6 more
wiley   +1 more source

Mouse ZGRF1 helicase facilitates DNA repair and maintains efficient fertility

open access: yesHeliyon
The recently characterised human ZGRF1 helicase promotes genomic stability by facilitating DNA interstrand crosslink repair. In its absence, human cells exhibit greater sensitivity towards anti-cancer drugs such as mitomycin C and camptothecin. Moreover,
Ernest Wee Kiat Lim   +9 more
doaj   +1 more source

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