Sort   by:  
 Page size 
UnknownS-2-hydroxyglutarate regulates CD8+ T-lymphocyte fate.
Not available
S-EPMC5149074 | biostudies-literature
UnknownReliability and Validity of a Home-Based Self-Administered Computerized Test of Learning and Memory Using Speech Recognition.
Not available
S-EPMC10081827 | biostudies-literature
TranscriptomicsAltered gene expression in Werner & Bloom syndromes is associated with sequences having G-quadruplex forming potential
The human Werner and Bloom syndromes (WS and BS) are caused by deficiencies in the WRN and BLM RecQ helicases, respectively. WRN, BLM and their S. cerevisiae homologue Sgs1, are particularly active in vitro in unwinding G-quadruplex DNA (G4-DNA), a family of non-canonical nucleic acid structures fo...
ORGANISM(S): Homo sapiens 
2009-12-09 | E-GEOD-19205 | biostudies-arrayexpress
UnknownLaparoscopic versus open parenchymal preserving liver resections in the posterosuperior segments (ORANGE Segments): a multicentre, single-blind, randomised controlled trial.
Not available
S-EPMC11889631 | biostudies-literature
TranscriptomicsGSTP1 expression predicts poor pathological complete response to neoadjuvant chemotherapy in ER-negative breast cancer
The purpose of the present study was to investigate the association of glutathione S-transferase P1 (GSTP1) expression with resistance to neoadjuvant paclitaxel followed by 5-fluorouracil/epirubicin/cyclophosphamide (P-FEC) in human breast cancers. The relationship of GSTP1 expression and GSTP1 prom...
ORGANISM(S): Homo sapiens 
2012-03-20 | E-GEOD-32646 | biostudies-arrayexpress
UnknownMeasurement of physiological recovery from exacerbation of chronic obstructive pulmonary disease using within-breath forced oscillometry.
Not available
S-EPMC2092458 | biostudies-literature
TranscriptomicsLoss of MeCP2 function is associated with distinct gene expression changes in the striatum
Rett syndrome (RTT) is a neurodevelopmental disorder characterized by developmental regression around 6-18 months after birth, followed by a lifetime of intellectual disability, stereotyped behaviors, and motor deficits. RTT is caused by mutations in MeCP2, a methyl-CpG binding protein that was trad...
ORGANISM(S): Mus musculus 
2013-07-13 | E-GEOD-42895 | biostudies-arrayexpress
UnknownThe S enantiomer of 2-hydroxyglutarate increases central memory CD8 populations and improves CAR-T therapy outcome.
Not available
S-EPMC7509862 | biostudies-literature
TranscriptomicsTranscription profiling of human decidua basalis to identify pre-eclampsia susceptibility genes
To identify mechanisms of genetic regulation within the decidual tissue of a retrospectively ascertained cohort of preeclamptic and non-preeclamptic Norwegian women.
ORGANISM(S): Homo sapiens 
2009-04-07 | E-TABM-682 | biostudies-arrayexpress
UnknownConcurrent validity of skin carotenoid status as a concentration biomarker of vegetable and fruit intake compared to multiple 24-h recalls and plasma carotenoid concentrations across one year: a cohort study.
Not available
S-EPMC6873686 | biostudies-literature
Sort   by:  
 Page size