Bibliographic record
Abstract
Pharmacogenetics postulates that interindividual variations in drug response are due to subtle genetic differences with little or no obvious phenotypes except in response to relevant drugs. Variations in treatment responses, manifested as drug resistance or adverse drug effects, could be due to polymorphisms in genes controlling drug transport, metabolism, disposition, targets, cell signaling, or cellular response pathways. Research carried out in recent years has allowed greater insight into the polymorphic content of genes and potential mechanisms by which inherited genetic variations affect function. These developments have accelerated studies assessing the association between relevant gene polymorphisms and variability in treatment responses. The identification of polymorphisms that contribute to this variability may lead to different treatment schedules, allowing for a reduction in drug side effects, while improving or maintaining the efficacy of treatment. This chapter will summarize the polymorphisms in genes that control pharmacokinetic and pharmacodynamic determinants of the response to treatment in acute lymphocytic leukemia (ALL). The majority of these studies have been performed in the pediatric population. Wherever available, the data on adult patients is described as well. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.
How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.004 | 0.007 |
| Meta-epidemiology (narrow) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.001 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.001 | 0.003 |
| Scholarly communication | 0.003 | 0.005 |
| Open science | 0.002 | 0.002 |
| Research integrity | 0.006 | 0.011 |
| Insufficient payload (model declined to judge) | 0.020 | 0.009 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".