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UnknownSystematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae).
Not available
S-EPMC8390884 | biostudies-literature
UnknownFactors affecting the sustainability of community mental health assets: A systematic review.
Not available
S-EPMC10087471 | biostudies-literature
UnknownEffect of a needs-based model of care on the characteristics of healthcare services in England: the i-THRIVE National Implementation Programme.
Not available
S-EPMC11955426 | biostudies-literature
Unknown'Shall We Send a Panda?' A Practical Guide to Engaging Schools in Research: Learning from Large-Scale Mental Health Intervention Trials.
Not available
S-EPMC8950538 | biostudies-literature
GenomicsUQ Data Access Commitee
Data Access Committee EGAC00001002686
EGAC00001002686 | EGA
TranscriptomicsSessile serrated adenomas and conventional adenomas of the colon
Sessile serrated adenomas are now recognized as precursor lesions of a substantial subset of colorectal cancers arising via a so-called “serrated pathway”. However, their biological markers remain to be defined. The aim of our study was to identify differentially expressed genes in sessile serrated ...
ORGANISM(S): Homo sapiens 
2008-08-26 | E-GEOD-12514 | biostudies-arrayexpress
ProteomicsA patient-based Drosophila model for mitochondrial S-Adenosylhomocysteine transport deficiency
The SLC25A26 gene encodes a mitochondrial inner membrane carrier that transports S-adenosylmethionine (SAM) into the mitochondrial matrix in exchange for S-adenosylhomocysteine (SAH). SAM is the predominant methyl-group donor for most cellular methylation processes, of which SAH is produced as a by-...
ORGANISM(S): Drosophila melanogaster (Fruit fly) 
2022-01-19 | PXD026900 | Pride
Sam Samc Methylation Sah Mitochondria Drosophila Slc25a26 
UnknownAn optogenetic method for interrogating YAP1 and TAZ nuclear-cytoplasmic shuttling.
Not available
S-EPMC8313864 | biostudies-literature
ProteomicsFactor H and related proteins in AMD
Age-related macular degeneration (AMD) is a common form of adult blindness. Risk of developing AMD is strongly linked to genetics, in particular at the Regulators of Complement Activation (RCA) locus on Chr1, which contains 6 genes, Complement Factor H (CFH) and Complement Factor H-related 1-5 (CFHR...
ORGANISM(S): Homo Sapiens 
2022-01-18 | PXD023466 | panorama
UnknownThe impact of universal, school based, interventions on help seeking in children and young people: a systematic literature review.
Not available
S-EPMC9837763 | biostudies-literature
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