 Peptidylprolyl Isomerase
"Peptidylprolyl Isomerase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme that catalyzes the isomerization of proline residues within proteins. EC 5.2.1.8.
| Descriptor ID |
D019696
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| MeSH Number(s) |
D08.811.399.325.500
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| Concept/Terms |
Peptidylprolyl Isomerase- Peptidylprolyl Isomerase
- Isomerase, Peptidylprolyl
- Peptidyl-Prolyl cis-trans-Isomerase
- Peptidyl Prolyl cis trans Isomerase
- cis-trans-Isomerase, Peptidyl-Prolyl
- Proline Isomerase
- Isomerase, Proline
- PPIase
- Prolyl Isomerase
- Isomerase, Prolyl
- Proline Rotamase
- Rotamase, Proline
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Below are MeSH descriptors whose meaning is more general than "Peptidylprolyl Isomerase".
Below are MeSH descriptors whose meaning is more specific than "Peptidylprolyl Isomerase".
This graph shows the total number of publications written about "Peptidylprolyl Isomerase" by people in UAMS Profiles by year, and whether "Peptidylprolyl Isomerase" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2023 | 0 | 1 | 1 | | 2020 | 1 | 0 | 1 | | 1992 | 0 | 1 | 1 |
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Below are the most recent publications written about "Peptidylprolyl Isomerase" by people in Profiles over the past ten years.
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Gandy K, Sapkota Y, Scoggins MA, Jacola LM, Koscik TR, Hudson MM, Pui CH, Krull KR, van der Plas E. Genetic variants, neurocognitive outcomes, and functional neuroimaging in survivors of childhood acute lymphoblastic leukemia. JNCI Cancer Spectr. 2023 07 03; 7(4).
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Chai G, Webb A, Li C, Antaki D, Lee S, Breuss MW, Lang N, Stanley V, Anzenberg P, Yang X, Marshall T, Gaffney P, Wierenga KJ, Chung BH, Tsang MH, Pais LS, Lovgren AK, VanNoy GE, Rehm HL, Mirzaa G, Leon E, Diaz J, Neumann A, Kalverda AP, Manfield IW, Parry DA, Logan CV, Johnson CA, Bonthron DT, Valleley EMA, Issa MY, Abdel-Ghafar SF, Abdel-Hamid MS, Jennings P, Zaki MS, Sheridan E, Gleeson JG. Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly. Neuron. 2021 01 20; 109(2):241-256.e9.
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