Results 131 to 140 of about 12,302,946 (299)

Molecular characterization of early-stage multi-primary lung adenocarcinoma by transcriptome sequencing—a retrospective study [PDF]

open access: yesPeerJ
Background To investigate the molecular genetic features of multiple primary lung cancer (MPLC) to provide a basis and new methods for its identification, diagnosis, and treatment.
Fang Zhang, Guangqiang Zhao
doaj   +2 more sources

Regulation of the lncRNA NEAT1 by p53‐ΔNp63 crosstalk modulates the DNA damage response and therapeutic efficacy in HNSCC

open access: yesMolecular Oncology, EarlyView.
In head and neck squamous cell carcinoma (HNSCC) p53 and p63 exert opposite roles on the transcription regulation of the lncRNA NEAT1. Under basal conditions, p53 levels are low and p63 represses NEAT1 expression. Upon genotoxic stress, p53 is rapidly induced, displacing p63 from the NEAT1 promoter leading to NEAT1 transcriptional activation and ...
Sara De Domenico   +5 more
wiley   +1 more source

Do MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium.

open access: yes, 2007
Association studies in large series of breast cancer patients can be used to identify single-nucleotide polymorphisms (SNP) contributing to breast cancer susceptibility.
Pharoah, Paul DP   +22 more
core   +1 more source

Multiple primary cancer with primary lung cancer in 986 autopsy cases.

open access: yesHaigan, 1986
剖検例986例を対象に, 肺癌を含む重複癌について検討した.肺癌を含む重複癌は28例で, 原発性肺癌206例の13.6%, 全重複癌81例の34.6%を占めていた.平均年齢は64.2才, 男女比は24対4で男性が圧倒的に多かった.組織型では扁平上皮癌10例、腺癌11例、小細胞癌5例, 大細胞癌5例 (肺内多発癌3例を含む) で, 各々の重複癌発生率は13~16%であった.顕性の第2癌15例の発見の糸口は, 胸部レ線異常が8例と多かったが, 7例は肺結核症や転移性肺癌とされた原発性肺癌であった.肺癌を含む重複癌28例の中間生存期間は, 8ヵ月であり, 肺癌先発例では7ヵ月, 後発例では26ヵ月, 後発例の肺癌発症後のそれは4ヵ月で, いずれも有意差を認めた.担癌体における ...
Fukuda, Yasuki   +6 more
openaire   +2 more sources

Polymorphisms of CYP1A1 I462V and GSTM1 genotypes and lung cancer susceptibility in Mongolian [PDF]

open access: yes, 2009
Aim: To study the genotype of cytochrome P450 1A1(CYP1A1) I462V and glutathions S-transferase M1( GSTM1) and the relationship of the genetic polymorphism of them with the susceptibility of lung cancer in Mongolia of China.
Guang Wang   +6 more
core  

Deep sequence analysis of non-small cell lung cancer: Integrated analysis of gene expression, alternative splicing, and single nucleotide variations in lung adenocarcinomas with and without oncogenic KRAS mutations [PDF]

open access: yes, 2012
KRAS mutations are highly prevalent in non-small cell lung cancer (NSCLC), and tumors harboring these mutations tend to be aggressive and resistant to chemotherapy.
David Rossell   +65 more
core   +1 more source

MULTIPLE PRIMARY CANCER OF THE LUNG

open access: yesJournal of Thoracic Surgery, 1958
C L, ROBINSON, C A, JACKSON
openaire   +2 more sources

Multifunctional role of PED/PEA15 in cell death and cell motility in human non small cell lung cancer (NSCLC) [PDF]

open access: yes, 2009
PED (phosphoprotein enriched in diabetes) is a 15 KDa protein involved in many cellular pathways and human diseases, including type II diabetes and cancer. We recently reported its overexpression in breast and lung cancers, and B-cell chronic lymphocytic
Zanca, Ciro
core   +1 more source

Identification and characterisation of calcitonin receptor isoforms expressed in glioblastoma derived glioma stem and U‐87 MG cells

open access: yesFEBS Open Bio, EarlyView.
Glioblastoma cells express calcitonin receptor variants (CT receptor isoforms) that may help them survive stress. Using qPCR, transcript‐specific long‐read nanopore sequencing, immunofluorescence co‐localisation and comparative sequence analysis, this study identifies a novel alternatively spliced CALCR transcript that encodes the CTb receptor isoform ...
Pragya Gupta   +7 more
wiley   +1 more source

The C‐terminal truncated splicing variant of NK1R negatively modulates substance P‐stimulated NK1R signaling

open access: yesFEBS Open Bio, EarlyView.
The neurokinin 1 receptor exists as full‐length (NK1L) and C‐terminally truncated (NK1S) splice variants. We show that NK1S heterodimerizes with NK1L, impairing Gαq coupling and Ca2+ mobilization while enhancing β‐arrestin1 recruitment. NK1S suppresses substance P‐driven gene expression and cell migration, revealing NK1S as an endogenous biased ...
Lan Phuong Nguyen   +8 more
wiley   +1 more source

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