FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2078191106> ?p ?o ?g. }

• W2078191106 endingPage "1133" @default.
• W2078191106 startingPage "1126" @default.
• W2078191106 abstract "Using comparative genomic hybridization (CGH), we investigated copy number aberrations in 29 esophageal squamous cell carcinoma (ESC) cell lines. All lines displayed numerous chromosome imbalances. The most frequent losses were observed on chromosome 18q (65.5%), Xp (48. 3%), 3p (44.8%), 4q (44.8%), 8p (41.4%), 11q23 - 25 (34.5%) and 4p (27.6%), whereas the most common copy number gains were noted at 8q (86.2%), 3q (82.8%), 5p (69%), 7p (69%), 20q (65.5%), 9q (55.2%), 11q (55.2%), 1q (48.3%), Xq (44.8%) and 18p (37.9%). High-level gains (HLGs) were detected at 3q26 (9 cases), 8q23 (6 cases), 5p14 - 15 (6 cases), 18p11.2 - 11.3 (6 cases), 3q27 - 28 (5 cases), 5p13 (3 cases), 7p14 - 15 (3 cases), 20q12 - 13 (3 cases), 11q13 (3 cases), 14q21 (2 cases), 20p11.2 (2 cases), 13q32 (2 case), and 1q32 (1 case). Among them, HLGs of 1q32 have been reported in other types of cancer, including glioblastoma and breast cancers. We successfully narrowed down the smallest common amplicon involving 1q-gain to the genomic segment between D1S414 and D1S2860 by fluorescence in situ hybridization (FISH). Southern and northern blot analysis clearly demonstrated that ATF3, human activating transcription factor-3 and CENPF, centromere protein F, mapped within this region, were significantly amplified and over-expressed in 1q32 amplicon." @default.
• W2078191106 created "2016-06-24" @default.
• W2078191106 creator A5005720957 @default.
• W2078191106 creator A5015825703 @default.
• W2078191106 creator A5042837518 @default.
• W2078191106 creator A5053191594 @default.
• W2078191106 creator A5061796459 @default.
• W2078191106 creator A5066745034 @default.
• W2078191106 creator A5073448109 @default.
• W2078191106 creator A5079171795 @default.
• W2078191106 creator A5090008088 @default.
• W2078191106 creator A5090644104 @default.
• W2078191106 date "2000-11-01" @default.
• W2078191106 modified "2023-10-13" @default.
• W2078191106 title "Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines: Possible Involvement of the<i>ATF3</i>and<i>CENPF</i>Genes in the 1q32 Amplicon" @default.
• W2078191106 cites W1544851750 @default.
• W2078191106 cites W155582688 @default.
• W2078191106 cites W1602404190 @default.
• W2078191106 cites W1608544625 @default.
• W2078191106 cites W1818207061 @default.
• W2078191106 cites W1827761694 @default.
• W2078191106 cites W1850623575 @default.
• W2078191106 cites W1909097318 @default.
• W2078191106 cites W1968046362 @default.
• W2078191106 cites W1971653050 @default.
• W2078191106 cites W1980717040 @default.
• W2078191106 cites W1998947396 @default.
• W2078191106 cites W2008005259 @default.
• W2078191106 cites W2013607771 @default.
• W2078191106 cites W2046652065 @default.
• W2078191106 cites W2056334142 @default.
• W2078191106 cites W2059072983 @default.
• W2078191106 cites W2064148182 @default.
• W2078191106 cites W2065081049 @default.
• W2078191106 cites W2069262022 @default.
• W2078191106 cites W2069839886 @default.
• W2078191106 cites W2072890996 @default.
• W2078191106 cites W2074809432 @default.
• W2078191106 cites W2119125180 @default.
• W2078191106 cites W2125492990 @default.
• W2078191106 cites W2125762535 @default.
• W2078191106 cites W2128433154 @default.
• W2078191106 cites W2140358910 @default.
• W2078191106 cites W2142448075 @default.
• W2078191106 cites W2143276239 @default.
• W2078191106 cites W2153764234 @default.
• W2078191106 cites W2157866949 @default.
• W2078191106 cites W2159568631 @default.
• W2078191106 cites W2161980752 @default.
• W2078191106 cites W2165409131 @default.
• W2078191106 cites W2169519454 @default.
• W2078191106 cites W2332419383 @default.
• W2078191106 cites W2400217513 @default.
• W2078191106 cites W2415484289 @default.
• W2078191106 cites W2416023135 @default.
• W2078191106 cites W4320995661 @default.
• W2078191106 doi "https://doi.org/10.1111/j.1349-7006.2000.tb00895.x" @default.
• W2078191106 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5926289" @default.
• W2078191106 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11092977" @default.
• W2078191106 hasPublicationYear "2000" @default.
• W2078191106 type Work @default.
• W2078191106 sameAs 2078191106 @default.
• W2078191106 citedByCount "71" @default.
• W2078191106 countsByYear W20781911062012 @default.
• W2078191106 countsByYear W20781911062013 @default.
• W2078191106 countsByYear W20781911062014 @default.
• W2078191106 countsByYear W20781911062016 @default.
• W2078191106 countsByYear W20781911062018 @default.
• W2078191106 countsByYear W20781911062021 @default.
• W2078191106 crossrefType "journal-article" @default.
• W2078191106 hasAuthorship W2078191106A5005720957 @default.
• W2078191106 hasAuthorship W2078191106A5015825703 @default.
• W2078191106 hasAuthorship W2078191106A5042837518 @default.
• W2078191106 hasAuthorship W2078191106A5053191594 @default.
• W2078191106 hasAuthorship W2078191106A5061796459 @default.
• W2078191106 hasAuthorship W2078191106A5066745034 @default.
• W2078191106 hasAuthorship W2078191106A5073448109 @default.
• W2078191106 hasAuthorship W2078191106A5079171795 @default.
• W2078191106 hasAuthorship W2078191106A5090008088 @default.
• W2078191106 hasAuthorship W2078191106A5090644104 @default.
• W2078191106 hasBestOaLocation W20781911061 @default.
• W2078191106 hasConcept C104317684 @default.
• W2078191106 hasConcept C124942203 @default.
• W2078191106 hasConcept C153911025 @default.
• W2078191106 hasConcept C2777542201 @default.
• W2078191106 hasConcept C2777546739 @default.
• W2078191106 hasConcept C30481170 @default.
• W2078191106 hasConcept C49105822 @default.
• W2078191106 hasConcept C502942594 @default.
• W2078191106 hasConcept C54355233 @default.
• W2078191106 hasConcept C8185291 @default.
• W2078191106 hasConcept C86803240 @default.
• W2078191106 hasConceptScore W2078191106C104317684 @default.
• W2078191106 hasConceptScore W2078191106C124942203 @default.
• W2078191106 hasConceptScore W2078191106C153911025 @default.
• W2078191106 hasConceptScore W2078191106C2777542201 @default.
• W2078191106 hasConceptScore W2078191106C2777546739 @default.
• W2078191106 hasConceptScore W2078191106C30481170 @default.

• next