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TranscriptomicsComplete OATP1B1 and OATP1B3 deficiency underlies human Rotor syndrome.
Rotor syndrome is an autosomal recessive disorder characterized by conjugated hyperbilirubinemia, near-absent hepatic uptake of anionic diagnostics, and coproporphyrinuria. The mechanistic basis of other hyperbilirubinemia syndromes is largely understood, but that of Rotor syndrome has remained enig...
ORGANISM(S): Homo sapiens 
2012-01-16 | E-GEOD-33733 | biostudies-arrayexpress
ProteomicsAssembly of the catalytic module and the rotor of human ATP synthase.
Human ATP synthase is a molecular rotary machine bound in inner mitochondrial membranes, built from twenty-eight subunits of seventeen kinds, two encoded in mitochondrial DNA, the remainder in nuclear genes. The machine consists of a rotor and an interacting stator. Turning of the rotor driven by a ...
ORGANISM(S): Homo sapiens (Human) 
2026-06-27 | PXD077889 | Pride
Human mitochondria/atp synthase/assembly/f1-module/rotor/lc-msms 
ProteomicsAssembly of the catalytic module and the rotor of human ATP synthase.
Human ATP synthase is a molecular rotary machine bound in inner mitochondrial membranes, built from twenty-eight subunits of seventeen kinds, two encoded in mitochondrial DNA, the remainder in nuclear genes. The machine consists of a rotor and an interacting stator. Turning of the rotor driven by a ...
ORGANISM(S): Homo sapiens (Human) 
2026-06-27 | PXD077960 | Pride
Human mitochondria/atp synthase/assembly/f1-module/rotor/lc-msms 
ProteomicsAssembly of the catalytic module and the rotor of human ATP synthase.
Human ATP synthase is a molecular rotary machine bound in inner mitochondrial membranes, built from twenty-eight subunits of seventeen kinds, two encoded in mitochondrial DNA, the remainder in nuclear genes. The machine consists of a rotor and an interacting stator. Turning of the rotor driven by a ...
ORGANISM(S): Homo sapiens (Human) 
2026-06-27 | PXD077924 | Pride
Lc-msms Human mitochondria/atp synthase/assembly/f1-module/rotor 
ProteomicsAssembly of the catalytic module and the rotor of human ATP synthase Pt V
Human ATP synthase is a molecular rotary machine bound in inner mitochondrial membranes, built from twenty-eight subunits of seventeen kinds, two encoded in mitochondrial DNA, the remainder in nuclear genes. The machine consists of a rotor and an interacting stator. Turning of the rotor driven by a ...
ORGANISM(S): Homo sapiens (Human) 
2026-06-27 | PXD079319 | Pride
Human mitochondria/atp synthase/assembly/f1-module/rotor/lc-msms 
ProteomicsAssembly of the catalytic module and the rotor of human ATP synthase Pt IV
Human ATP synthase is a molecular rotary machine bound in inner mitochondrial membranes, built from twenty-eight subunits of seventeen kinds, two encoded in mitochondrial DNA, the remainder in nuclear genes. The machine consists of a rotor and an interacting stator. Turning of the rotor driven by a ...
ORGANISM(S): Homo sapiens (Human) 
2026-06-27 | PXD079310 | Pride
Lc-msms Atp synthase Human mitochondria Assembly F1-module Rotor 
GenomicsComplete OATP1B1 and OATP1B3 deficiency underlies human Rotor syndrome.
Rotor syndrome is an autosomal recessive disorder characterized by conjugated hyperbilirubinemia, near-absent hepatic uptake of anionic diagnostics, and coproporphyrinuria. The mechanistic basis of other hyperbilirubinemia syndromes is largely understood, but that of Rotor syndrome has remained enig...
ORGANISM(S): Homo sapiens 
2012-01-16 | GSE33733 | GEO
UnknownDroplet distribution in cotton canopy using single-rotor and four-rotor unmanned aerial vehicles.
Not available
S-EPMC9205310 | biostudies-literature
GenomicsHomo sapiens
Complete OATP1B1 and OATP1B3 deficiency underlies human Rotor syndrome.
PRJNA148433 | ENA
UnknownQuantum rotor in nanostructured superconductors.
Not available
S-EPMC3971402 | biostudies-literature
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