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UnknownAXL promotes lymphangiogenesis by amplifying VEGF-C-mediated AKT pathway.
Not available
S-EPMC11865408 | biostudies-literature
UnknownFOXO1 forkhead domain mutants in B-cell lymphoma lack transcriptional activity.
Not available
S-EPMC8789783 | biostudies-literature
UnknownCDC-48/p97 coordinates CDT-1 degradation with GINS chromatin dissociation to ensure faithful DNA replication.
Not available
S-EPMC3428722 | biostudies-literature
UnknownPhenotypes in siblings with homozygous mutations of TRAPPC9 and/or MCPH1 support a bifunctional model of MCPH1.
Not available
S-EPMC6081227 | biostudies-literature
UnknownREG-O3 chimeric peptide combining growth hormone and somatostatin sequences improves joint function and prevents cartilage degradation in rat model of traumatic knee osteoarthritis.
Not available
S-EPMC7156079 | biostudies-literature
UnknownAtypical haemolytic uraemic syndrome associated with a hybrid complement gene.
Not available
S-EPMC1626556 | biostudies-literature
UnknownScreening of highly expressed mycobacterial genes identifies Rv3615c as a useful differential diagnostic antigen for the Mycobacterium tuberculosis complex.
Not available
S-EPMC2519431 | biostudies-literature
UnknownSevere congenital microcephaly with AP4M1 mutation, a case report.
Not available
S-EPMC5414176 | biostudies-literature
UnknownPutative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families.
Not available
S-EPMC10108251 | biostudies-literature
UnknownAn alternative role of FoF1-ATP synthase in Escherichia coli: synthesis of thiamine triphosphate.
Not available
S-EPMC3545222 | biostudies-literature
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