Evidence map›Paper›PMID 34054524›Full record

ArticleFrontiers in pharmacology2021

Informing Pharmacokinetic Models With Physiological Data: Oral Population Modeling of L-Serine in Humans.

J R Bosley, Elias Björnson, Cheng Zhang, Hasan Turkez, Jens Nielsen, Mathias Uhlen, Jan Borén, Adil Mardinoglu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Pharmacokinetics of oral l-serine supplementation in a single patient.Molecular genetics and metabolism reports · 2020
    Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 3 countries.

J R BosleyClermont Bosley LLC, Philadelphia, PA, United States.
Elias BjörnsonDepartment of Molecular and Clinical Medicine, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.
Cheng ZhangScience for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, Sweden.
Hasan TurkezDepartment of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum, Turkey.
Jens NielsenDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Mathias UhlenScience for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, Sweden.
Jan BorénDepartment of Molecular and Clinical Medicine, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.
Adil MardinogluScience for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, Sweden.
Science for Life Laboratory · SEAtatürk University · TRChalmers University of Technology · SEKTH Royal Institute of Technology · SESahlgrenska University Hospital · SEUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To determine how to set optimal oral L-serine (serine) dose levels for a clinical trial, existing literature was surveyed. Data sufficient to set the dose was inadequate, and so an (

Indexed as

L-Serine (ser)NAFLD (non alcoholic fatty liver disease)oral supplementationPharmacokinecticssystems biology

Identifiers

PMID34054524
PMCPMC8156419
OpenAlexW3163140091

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.