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UnknownFabrication of an anatomy-mimicking BIO-AIR-TUBE with engineered cartilage.
Not available
S-EPMC6700413 | biostudies-literature
UnknownBile acid profiles in adult patients with biliary atresia who achieve native liver survival after portoenterostomy.
Not available
S-EPMC10827714 | biostudies-literature
UnknownGeneration and transcriptome profiling of bonobo induced pluripotent stem cells using stealth RNA vectors: a tripartite comparative study with humans and chimpanzees.
Not available
S-EPMC12797634 | biostudies-literature
TranscriptomicsDevelopmental gene expression of Xenopus laevis J strain [stage]
Comprehensive RNA-seq experiments to measure the expression of homoeologs across different developmental stages, as a part of the Xenopus laevis genome project. This work is funded by Agency Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT; "Genome Science" Gra...
ORGANISM(S): Xenopus laevis 
2016-10-24 | E-GEOD-73430 | biostudies-arrayexpress
TranscriptomicsTissue gene expression of Xenopus laevis J strain [tissue]
Comprehensive RNA-seq experiments to measure the expression of homoeologs across different tissues, as a part of the Xenopus laevis genome project. This work is funded by Agency Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT; "Genome Science" Grant ID 221S000...
ORGANISM(S): Xenopus laevis 
2016-10-24 | E-GEOD-73419 | biostudies-arrayexpress
UnknownImpaired cortico-striatal excitatory transmission triggers epilepsy.
Not available
S-EPMC6478892 | biostudies-literature
UnknownFLT3-ITD transduces autonomous growth signals during its biosynthetic trafficking in acute myelogenous leukemia cells.
Not available
S-EPMC8608843 | biostudies-literature
MetabolomicsGNPS - Bile acid dehydroxylation by the gut microbiome
A metabolic pathway for bile acid dehydroxylation by the gut microbiome
ORGANISM(S): Clostridium (ncbitaxon:1485) 
2020-03-02 | MSV000085048 | GNPS
UnknownMultiple common and rare variants of ABCG2 cause gout.
Not available
S-EPMC5706492 | biostudies-literature
UnknownIdentification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families.
Not available
S-EPMC7733723 | biostudies-literature
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