"Mutation" 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.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
| Descriptor ID |
D009154
|
| MeSH Number(s) |
G05.365.590
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Mutation".
Below are MeSH descriptors whose meaning is more specific than "Mutation".
This graph shows the total number of publications written about "Mutation" by people in this website by year, and whether "Mutation" 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 |
|---|
| 1994 | 0 | 5 | 5 |
| 1995 | 3 | 5 | 8 |
| 1996 | 3 | 7 | 10 |
| 1997 | 2 | 8 | 10 |
| 1998 | 3 | 6 | 9 |
| 1999 | 4 | 16 | 20 |
| 2000 | 4 | 13 | 17 |
| 2001 | 3 | 14 | 17 |
| 2002 | 3 | 16 | 19 |
| 2003 | 2 | 31 | 33 |
| 2004 | 11 | 31 | 42 |
| 2005 | 9 | 42 | 51 |
| 2006 | 18 | 22 | 40 |
| 2007 | 6 | 30 | 36 |
| 2008 | 15 | 23 | 38 |
| 2009 | 12 | 26 | 38 |
| 2010 | 14 | 34 | 48 |
| 2011 | 9 | 27 | 36 |
| 2012 | 14 | 23 | 37 |
| 2013 | 14 | 31 | 45 |
| 2014 | 11 | 28 | 39 |
| 2015 | 22 | 39 | 61 |
| 2016 | 16 | 33 | 49 |
| 2017 | 11 | 31 | 42 |
| 2018 | 7 | 25 | 32 |
| 2019 | 15 | 29 | 44 |
| 2020 | 9 | 25 | 34 |
| 2021 | 7 | 28 | 35 |
| 2022 | 2 | 11 | 13 |
| 2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Causes of Clonal Hematopoiesis: a Review. Curr Oncol Rep. 2023 Mar; 25(3):211-220.
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Novel high-risk acute myeloid leukemia subgroup with ERG amplification and Biallelic loss of TP53. Cancer Genet. 2023 04; 272-273:23-28.
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PGRN deficiency exacerbates, whereas a brain penetrant PGRN derivative protects, GBA1 mutation-associated pathologies and diseases. Proc Natl Acad Sci U S A. 2023 01 03; 120(1):e2210442120.
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Inhibition of RAS-driven signaling and tumorigenesis with a pan-RAS monobody targeting the Switch I/II pocket. Proc Natl Acad Sci U S A. 2022 10 25; 119(43):e2204481119.
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Discovery of nonautonomous modulators of activated Ras. G3 (Bethesda). 2022 09 30; 12(10).
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Mutations of tyrosine 467 in the human norepinephrine transporter attenuate HIV-1 Tat-induced inhibition of dopamine transport while retaining physiological function. PLoS One. 2022; 17(9):e0275182.
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Do CPVT-linked mutations alter RYR2 regulation by cytosolic Ca2+ in cardiomyocytes? J Gen Physiol. 2022 09 05; 154(9).
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A case report of CFTR modulator administration via carrier mother to treat meconium ileus in a F508del homozygous fetus. J Cyst Fibros. 2022 07; 21(4):721-724.
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Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7Ra Chain. Front Immunol. 2022; 13:867837.
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Rapid expansion and extinction of antibiotic resistance mutations during treatment of acute bacterial respiratory infections. Nat Commun. 2022 03 09; 13(1):1231.