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UnknownExploring the role of professional identity in the implementation of clinical decision support systems-a narrative review.
Not available
S-EPMC10860285 | biostudies-literature
UnknownUnveiling the Structure-Property Relationship of MgO-Supported Ni Ammonia Decomposition Catalysts from Bulk to Atomic Structure by In Situ/Operando Studies.
Not available
S-EPMC10913046 | biostudies-literature
ProteomicsMycofactocin is critical for Mycobacterium tuberculosis adaptation into microaerophilic conditions
Mycofactocin is a new class of peptide-derived redox cofactor whose structural elucidation and functional characterization have recently received enormous focus. Among the six-gene cluster, mftD mediates a probable penultimate step in mycofactocin biosynthesis. MftD is a putative lactate dehydrogena...
ORGANISM(S): Mycobacterium smegmatis 
2021-07-05 | PXD023045 | Pride
Mycobacterium tuberculosis Hypoxia Mycofactocin Redox regulationamyloid formation Redox regulation Lactate metabolism 
ProteomicsAATF/Che-1 binds ribosome-associated RNAs and regulates ribosome biogenesis
AATF is a predominantly nuclear protein that has been shown to be an apoptosis-inhibiting factor essential for both embryonic development and tumor growth. Several studies have shown a role of AATF in the modulation of pivotal cellular signal transduction pathways such as p53-, mTOR- and HIF-signali...
ORGANISM(S): Homo sapiens (Human) 
2019-08-13 | PXD011055 | Pride
Aatf 
TranscriptomicsGene expression profiling of skeletal myoblast differentiation and exposure to TNF-alpha or IGF1
Skeletal myocyte differentiation involves fusion of myoblasts to multinucleated myotubes. In vitro differentiation can be induced by serum withdrawal. The differentiation process is negatively regulated by pathological concentrations of TNF-alpha but can be positively regulated by IGF1. This study f...
ORGANISM(S): Mus musculus 
2015-04-05 | E-MTAB-3474 | biostudies-arrayexpress
UnknownThe role of cyclin D1 and Ki-67 in the development and prognostication of thin melanoma.
Not available
S-EPMC7540531 | biostudies-literature
UnknownConnexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
Not available
S-EPMC379233 | biostudies-literature
UnknownNew insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
Not available
S-EPMC4592086 | biostudies-literature
UnknownThe Friends of Cancer Research Real-World Data Collaboration Pilot 2.0: Methodological Recommendations from Oncology Case Studies.
Not available
S-EPMC9298732 | biostudies-literature
UnknownDMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
Not available
S-EPMC5942547 | biostudies-literature
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