Results 71 to 80 of about 93,598 (304)

Genomic Distribution of Simple Sequence Repeats in Brassica rapa

open access: yesMolecules and Cells, 2007
Simple Sequence Repeats (SSRs) represent short tandem duplications found within all eukaryotic organisms. To examine the distribution of SSRs in the genome of Brassica rapa ssp. pekinensis, SSRs from different genomic regions representing 17.7 Mb of genomic sequence were surveyed.
Hong, Chang Pyo   +9 more
openaire   +4 more sources

Network divergence analysis identifies adaptive gene modules and two orthogonal vulnerability axes in pancreatic cancer

open access: yesMolecular Oncology, EarlyView.
Tumors contain diverse cellular states whose behavior is shaped by context‐dependent gene coordination. By comparing gene–gene relationships across biological contexts, we identify adaptive transcriptional modules that reorganize into distinct vulnerability axes.
Brian Nelson   +9 more
wiley   +1 more source

List of simple sequence repeats.

open access: yes, 2014
aThe SSR-containing coding regions are indicated in parentheses. SSRs that are identical in the C. sinensis chloroplast genome are highlighted in bold; SSRs that are conserved but with different lengths are highlighted by underline.List of simple ...
Huei-Jiun Su (661213)   +3 more
core   +1 more source

Statistics of Simple Sequence Repeats (SSRs) taxonomy of Coix lacryma-jobi L.

open access: yes, 2021
Statistics of Simple Sequence Repeats (SSRs) taxonomy of Coix lacryma-jobi L.
Qingxia Zhang (5982191)   +4 more
core   +1 more source

COMP–PMEPA1 axis promotes epithelial‐to‐mesenchymal transition in breast cancer cells

open access: yesMolecular Oncology, EarlyView.
This study reveals that cartilage oligomeric matrix protein (COMP) promotes epithelial‐to‐mesenchymal transition (EMT) in breast cancer. We identify PMEPA1 (protein TMEPAI) as a novel COMP‐binding partner that mediates EMT via binding to the TSP domains of COMP, establishing the COMP–PMEPA1 axis as a key EMT driver in breast cancer.
Konstantinos S. Papadakos   +6 more
wiley   +1 more source

Comprehensive Analysis of Simple Sequence Repeats in Pre-miRNAs [PDF]

open access: yesMolecular Biology and Evolution, 2010
Simple sequence repeats (SSRs) are tandem repeat units of 1-6 bp that are identified in various complete sequences. However, the distribution, nature, and origination of SSRs in pre-miRNAs, which are characteristic stem-loop sequences and are finally processed into ∼22 nt functional miRNAs contributing to regulate several biological processes, are ...
Ming, Chen   +3 more
openaire   +2 more sources

CCDC80 suppresses high‐grade serous ovarian cancer migration via negative regulation of B7‐H3

open access: yesMolecular Oncology, EarlyView.
PAX8 is a lineage‐specific master regulator of transcription in high‐grade serous ovarian cancer (HGSC) progression. We show for the first time that PAX8 facilitates proliferation and metastasis by repressing the cell autonomous tumor suppressor CCDC80 and inducing B7‐H3 expression.
Aya Saleh   +12 more
wiley   +1 more source

Fusarium oxysporum f. sp. phaseoli genetic variability assessed by new developed microsatellites

open access: yesGenetics and Molecular Biology
Fusarium oxysporum f. sp. phaseoli (Fop) J.B. Kendrich & W.C. Snyder is the causal agent of Fusarium wilt of common bean (Phaseolus vulgaris L.). The objective of this study was to develop microsatellite markers (SSRs) to characterize the genetic ...
Graziéle R. Sasseron   +6 more
doaj   +1 more source

Summary of simple sequence repeats (SSRs) in L. ruprechtiana cp genome.

open access: yes, 2022
Summary of simple sequence repeats (SSRs) in L. ruprechtiana cp genome.
Qingbei Weng (4983476)   +5 more
core   +1 more source

Heterozygous loss‐of‐function alleles associate the conserved 3′‐5′ exoribonuclease EXOSC10 with hypersensitivity to the anticancer drug 5‐fluorouracil

open access: yesMolecular Oncology, EarlyView.
EXOSC10, an essential nuclear RNA exosome‐associated 3′‐5′ exoribonuclease, is inhibited by the anticancer drug 5‐fluorouracil (5‐FU), and EXOSC10 depletion increases 5‐FU sensitivity. The colon‐cancer variant EXOSC10S402T, located in a proteolysis motif, is stable and nuclear but nonfunctional in vivo.
Radhika Sain   +10 more
wiley   +1 more source

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