beta endorphin inhibits ACh turnover in nuclei of rat brain

Just-in-Time Compound Pooling Increases Primary Screening Capacity without Compromising Screening Quality.

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Development of infant baboons' responses to graded bark variants.

Proceedings. Biological sciences·2001

Library design and virtual screening using multiple 4-point pharmacophore fingerprints.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2000

Proximate factors mediating "contact" calls in adult female baboons (Papio cynocephalus ursinus) and their infants.

Journal of comparative psychology (Washington, D.C. : 1983)·2000

Design and structure-activity relationships of potent and selective inhibitors of blood coagulation factor Xa.

Journal of medicinal chemistry·1999

Sulfonamidopyrrolidinone factor Xa inhibitors: potency and selectivity enhancements via P-1 and P-4 optimization.

Journal of medicinal chemistry·1999

An operational perturbation proteomics-based virtual cell model.

Nature·2026

Integrated signatures define mutational processes in prostate cancer.

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Imaging cellular activity across all organs reveals body-wide circuits.

Nature·2026

Neocortical long-range inhibition promotes cortical synchrony and sleep.

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TRI-611, a selective, brain-penetrant molecular glue degrader of ALK.

Nature·2026

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Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine·2026

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Food science & nutrition·2026

Association of betel quid chewing with specific major psychiatric disorders in Taiwan Biobank-NHIRD linked data.

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GLP-1 Receptor Agonists Post-Bariatric Surgery (GRABS) Trial: Rationale, Design and Baseline Characteristics.

Diabetes, obesity & metabolism·2026

Efficacy of protocol-based blood pressure management in the outpatient settings.

Journal of human hypertension·2026

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beta endorphin inhibits ACh turnover in nuclei of rat brain

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Just-in-Time Compound Pooling Increases Primary Screening Capacity without Compromising Screening Quality.

Development of infant baboons' responses to graded bark variants.

Library design and virtual screening using multiple 4-point pharmacophore fingerprints.

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Design and structure-activity relationships of potent and selective inhibitors of blood coagulation factor Xa.

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