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UnknownLarge-scale forest restoration stabilizes carbon under climate change in Southwest United States.
Not available
S-EPMC6916600 | biostudies-literature
UnknownDigital App for Speech and Health Monitoring Study (DASH): protocol for a prospective longitudinal case-control observational study for developing speech datasets in neurodegenerative disorders and dementia.
Not available
S-EPMC12684189 | biostudies-literature
MetabolomicsGut Microbiome Composition Is Associated With Future Onset of Crohn's Disease in Healthy First-Degree Relatives.

BACKGROUND & AIMS: The cause of Crohn's disease (CD) is unknown, but the current hypothesis is that microbial or environmental factors induce gut inflammation in genetically susceptible individuals, leading to chronic intestinal inflammation. Case-control studies of patients...

2023-11-16 | MTBLS300 | MetaboLights
GenomicsDAC for EGAS00001002275
Data Access Committee EGAC00001000600
EGAC00001000600 | EGA
UnknownRecessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73.
Not available
S-EPMC4511861 | biostudies-literature
UnknownStructural plasticity of the coiled-coil interactions in human SFPQ.
Not available
S-EPMC11754644 | biostudies-literature
UnknownTart Cherry Reduces Inflammation in Adipose Tissue of Zucker Fatty Rats and Cultured 3T3-L1 Adipocytes.
Not available
S-EPMC6266132 | biostudies-literature
GenomicsWhole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Chromosome 22q11.2 microdeletions impart a high but incomplete risk for schizophrenia. Possible mechanisms include genome-wide effects of DGCR8 haploinsufficiency. In a proof-of-principle study to assess the power of this model, we used high-quality, whole-genome sequencing of nine individuals with ...
EGAS00001002344 | EGA
UnknownAssociations between hematology/oncology fellows' training and mentorship experiences and hematology-only career plans.
Not available
S-EPMC6855099 | biostudies-literature
UnknownGenotypes and phenotypes of motor neuron disease: an update of the genetic landscape in Scotland.
Not available
S-EPMC11319561 | biostudies-literature
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