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UnknownIntegrating Women and Girls' Nutrition Services into Health Systems in Low- and Middle-Income Countries: A Systematic Review.
Not available
S-EPMC9657561 | biostudies-literature
UnknownMalnutrition in infants aged under 6 months: prevalence and anthropometric assessment - analysis of 56 low- and middle-income country DHS datasets.
Not available
S-EPMC12142141 | biostudies-literature
ProteomicsJNK-regulated phosphoproteome links synaptic and metabolic pathways to mood regulation
JNKs play critical roles in neuronal damage associated with neurodegenerative disease and inhibitors of JNK1 have shown anxiolytic and anti-depressive effects in mice. In this study, we analyze the phosphoproteomes of hippocampus and nucleus accumbens in mice treated with DJNKI-1, a JNK inhibitor.
ORGANISM(S): Mus musculus (Mouse) 
2025-12-02 | PXD060057 | Pride
ProteomicsRegulators of proteostasis are translationally repressed in fibroblasts from sporadic and LRRK2-G2019S Parkinson’s patients
Here we used non-canonical amino acid labeling and mass-spectrometry based proteomics to perform a quantitative comparison of nascent proteins in fibroblasts from sporadic and G2019S mutation PD patients compared to healthy individuals. We found that several proteins were under-represented among ...
ORGANISM(S): Homo sapiens (Human) 
2022-02-21 | PXD031144 | Pride
Parkinson's disease Protein synthesis 
UnknownExcretory-secretory products from the brown stomach worm, Teladorsagia circumcincta, exert antimicrobial activity in in vitro growth assays.
Not available
S-EPMC9528173 | biostudies-literature
TranscriptomicsHistone deacetylase inhibitors antagonize distinct pathways to suppress tumorigenesis of embryonal rhabdomyosarcoma.
Embryonal rhabdomyosarcoma (ERMS) is the most common soft tissue cancer in children and is characterized by myogenic differentiation arrest. The prognosis of patients with relapsed or metastatic disease remains poor. ERMS genomes show few recurrent mutations, suggesting that other molecular mechani...
ORGANISM(S): Homo sapiens 
2015-12-21 | E-GEOD-74970 | biostudies-arrayexpress
GenomicsInherited Predisposition to Cancer Projects Data Access Committee
Data Access Committee EGAC00001001565
EGAC00001001565 | EGA
GenomicsGenomic study of an AT-AML
Ataxia Telangiectasia (A-T) is caused by biallelic mutations in ATM and confers predisposition to cancer, with acute myeloid leukaemia (AML) being rarely observed. We investigated an AML arising in an A-T patient for secondary genetic events by performing whole exome sequencing of serial samples ove...
EGAS00001004392 | EGA
UnknownRTOG 9804: a prospective randomized trial for good-risk ductal carcinoma in situ comparing radiotherapy with observation.
Not available
S-EPMC4334775 | biostudies-literature
Genomics98be40b5-5141-4ceb-8723-6ddc59a9cda6 - samples
Serial samples from one AT-AML patient as described in publication Goldgraben et al Pediatric Blood & Cancer 2020. Whole exome sequencing of a AT-'germline' blood sample, one bone marrow sample (at AML diagnosis) and 3 AML blood samples. Library preped using the Illumina Nextera Rapid Capture Exom...
EGAD00001006090 | EGA
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