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UnknownAdolescent, Parent, and Provider Perceptions of a Predictive Algorithm to Identify Adolescent Suicide Risk in Primary Care.
Not available
S-EPMC11056301 | biostudies-literature
UnknownDexamethasone and High-Dose Methotrexate Improve Outcome for Children and Young Adults With High-Risk B-Acute Lymphoblastic Leukemia: A Report From Children's Oncology Group Study AALL0232.
Not available
S-EPMC4981974 | biostudies-literature
UnknownAcceptability, Engagement, and Effects of a Mobile Digital Intervention to Support Mental Health for Young Adults Transitioning to College: Pilot Randomized Controlled Trial.
Not available
S-EPMC8554670 | biostudies-literature
UnknownDasatinib Plus Intensive Chemotherapy in Children, Adolescents, and Young Adults With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: Results of Children's Oncology Group Trial AALL0622.
Not available
S-EPMC6067800 | biostudies-literature
UnknownIncreased burden of cardiovascular risk among youth suicide attempters.
Not available
S-EPMC8053730 | biostudies-literature
ProteomicsEarly-adulthood spike in protein translation drives aging via juvenile hormone/germline signaling
Protein translation (PT) declines with age in invertebrates, rodents, and humans. It has been assumed that elevated PT at young ages is beneficial to health and PT ends up dropping as a passive byproduct of aging. In Drosophila, we show that a transient elevation in PT during early-adulthood exerts ...
ORGANISM(S): Drosophila melanogaster (Fruit fly) 
2023-10-24 | PXD044118 | Pride
Proteostasis Aging Proteomics Lcms2 Drosophila 
UnknownChaperone biomarkers of lifespan and penetrance track the dosages of many other proteins.
Not available
S-EPMC6914778 | biostudies-literature
UnknownChildhood maltreatment, neuropsychological function and suicidal behavior.
Not available
S-EPMC6837731 | biostudies-literature
UnknownModern Solutions for Ancient Pathogens: Direct Pathogen Sequencing for Diagnosis of Lepromatous Leprosy and Cerebral Coenurosis.
Not available
S-EPMC9472670 | biostudies-literature
TranscriptomicsMutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2 [04_Cerebellun_and_brain]
Senataxin, encoded by the SETX gene, contributes to multiple aspects of gene expression, including transcription and RNA processing. Mutations in SETX cause the recessive disorder ataxia with oculomotor apraxia type 2 (AOA2) and a dominant juvenile form of amyotrophic lateral sclerosis (ALS4). To as...
ORGANISM(S): Mus musculus 
2014-09-15 | E-GEOD-61324 | biostudies-arrayexpress
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