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UnknownEffects of substitution and high-dose thyroid hormone therapy on deiodination, sulfoconjugation, and tissue thyroid hormone levels in prolonged critically ill rabbits.
Not available
S-EPMC2488214 | biostudies-literature
UnknownHeritable variation in maternally derived yolk androgens, thyroid hormones and immune factors.
Not available
S-EPMC4981687 | biostudies-literature
TranscriptomicsTranscriptional profile of the abdomen of zebrafish deiodinase knockdown
The role of deiodinase-mediated TH effects in early vertebrate development is only partially understood. Therefore, we investigated the role of deiodinases during early development of zebrafish until 96 hours post fertilization at the level of the transcriptome, biochemistry, morphology and physiolo...
ORGANISM(S): Danio rerio 
2015-04-10 | E-GEOD-61623 | biostudies-arrayexpress
TranscriptomicsTranscriptional profile of the tail of zebrafish deiodinase knockdown
The role of deiodinase-mediated TH effects in early vertebrate development is only partially understood. Therefore, we investigated the role of deiodinases during early development of zebrafish until 96 hours post fertilization at the level of the transcriptome, biochemistry, morphology and physiolo...
ORGANISM(S): Danio rerio 
2015-04-10 | E-GEOD-61624 | biostudies-arrayexpress
UnknownEarly stage of erythrocyte sedimentation rate test: Fracture of a high-volume-fraction gel.
Not available
S-EPMC10735292 | biostudies-literature
UnknownBroadband reconfigurable logic gates in phonon waveguides.
Not available
S-EPMC5630582 | biostudies-literature
UnknownScreening the RFX6-DNA binding domain for potential genetic variants in patients with type 2 diabetes.
Not available
S-EPMC6422854 | biostudies-literature
UnknownDrosophila distal-less and Rotund bind a single enhancer ensuring reliable and robust bric-a-brac2 expression in distinct limb morphogenetic fields.
Not available
S-EPMC3694829 | biostudies-literature
ProteomicsLiver Steatosis and Mitochondrial Dysfunction in Spinal Muscular Atrophy is Survival Motor Neuron-Dependent and Hepatocyte-Intrinsic
Spinal Muscular Atrophy (SMA) is typically characterized as a motor neuron disease, but extra-neuronal phenotypes are present in almost every organ in severely affected patients and animal models. Extra-neuronal phenotypes were previously underappreciated as patients with severe SMA phenotypes usual...
ORGANISM(S): Homo Sapiens (human) 
2024-05-09 | PXD045401 | JPOST Repository
UnknownReal-world analysis of healthcare resource utilization by patients with X-linked myotubular myopathy (XLMTM) in the United States.
Not available
S-EPMC10242920 | biostudies-literature
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