Sort   by:  
 Page size 
UnknownPhase I Trial of the Human Double Minute 2 Inhibitor MK-8242 in Patients With Advanced Solid Tumors.
Not available
S-EPMC5946729 | biostudies-literature
TranscriptomicsCIT-CHEF
Fibrolamellar hepatocellular carcinoma (FLC) is a rare type of primary liver cancer that often arises in children, adolescents and young adults. At the pathological level, FLC display pure morphology or can present with mixed morphology involving a conventional HCC component. Owing to the rarity of ...
ORGANISM(S): Homo sapiens 
2015-06-15 | E-MTAB-2675 | biostudies-arrayexpress
TranscriptomicsMitochondrial carrier SLC25A34 links clock, diet, and temperature control of adipocyte lipid cycling
BAT transcriptome from control and brown adipocyte-specific Rev-erbα/β double knockout mice housed at thermoneutrality or cold-challenged for 6 hours. Brown adipose tissue (BAT) samples were collected from control and brown adipocyte-specific Rev-erbα/β double knockout mice (Ucp1-Cre; Nr1d1/2 fl/fl)...
ORGANISM(S): Mus musculus 
2026-09-23 | E-MTAB-17580 | biostudies-arrayexpress
TranscriptomicsMapping of the HUWE1 duplication at Xp11.22 in eight unrelated XLID patients
In a study to elucidate the genetic defects in patients with X-linked intellectual disability (XLID) we performed X chromosome-specific BAC-array-CGH and identified 0.33 to 1.0 Mb nonrecurrent copy number gains at Xp11.22 in affected males of unrelated XLID families. All aberrations segregate with t...
ORGANISM(S): Homo sapiens 
2012-09-03 | E-GEOD-32945 | biostudies-arrayexpress
UnknownSubmicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
Not available
S-EPMC2426915 | biostudies-literature
UnknownPrediction of persistent incomplete occlusion of intracranial aneurysms treated with woven EndoBridge device.
Not available
S-EPMC11928387 | biostudies-literature
UnknownFederated learning enables big data for rare cancer boundary detection.
Not available
S-EPMC9722782 | biostudies-literature
UnknownThe psychiatric phenotypes of 1q21 distal deletion and duplication.
Not available
S-EPMC7862693 | biostudies-literature
UnknownStructure-based classification predicts drug response in EGFR-mutant NSCLC.
Not available
S-EPMC8481125 | biostudies-literature
UnknownA mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Not available
S-EPMC8206404 | biostudies-literature
Sort   by:  
 Page size