"Point 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.
A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair.
Descriptor ID |
D017354
|
MeSH Number(s) |
G05.365.590.675
|
Concept/Terms |
Point Mutation- Point Mutation
- Mutation, Point
- Mutations, Point
- Point Mutations
|
Below are MeSH descriptors whose meaning is more general than "Point Mutation".
Below are MeSH descriptors whose meaning is more specific than "Point Mutation".
This graph shows the total number of publications written about "Point Mutation" by people in this website by year, and whether "Point 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 |
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1994 | 10 | 2 | 12 |
1995 | 7 | 8 | 15 |
1996 | 3 | 4 | 7 |
1997 | 10 | 13 | 23 |
1998 | 1 | 12 | 13 |
1999 | 4 | 5 | 9 |
2000 | 8 | 5 | 13 |
2001 | 3 | 1 | 4 |
2002 | 2 | 4 | 6 |
2003 | 3 | 8 | 11 |
2004 | 1 | 3 | 4 |
2005 | 2 | 6 | 8 |
2006 | 1 | 3 | 4 |
2007 | 2 | 5 | 7 |
2008 | 3 | 3 | 6 |
2009 | 2 | 4 | 6 |
2010 | 0 | 4 | 4 |
2011 | 0 | 3 | 3 |
2012 | 1 | 5 | 6 |
2013 | 5 | 2 | 7 |
2014 | 0 | 1 | 1 |
2015 | 0 | 4 | 4 |
2016 | 1 | 1 | 2 |
2018 | 0 | 1 | 1 |
2019 | 1 | 1 | 2 |
2021 | 0 | 2 | 2 |
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Below are the most recent publications written about "Point Mutation" by people in Profiles.
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The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes. RNA. 2021 09; 27(9):1017-1024.
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Clear Cell Papillary Cystadenoma of the Ovary Masquerading as Metastatic Clear Cell Renal Cell Carcinoma: A Case Report and Review of the Literature. Int J Gynecol Pathol. 2021 May 01; 40(3):290-295.
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Rb family-independent activating E2F increases genome stability, promotes homologous recombination, and decreases non-homologous end joining. Mech Dev. 2020 06; 162:103607.
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Somatic mitochondrial mutation discovery using ultra-deep sequencing of the mitochondrial genome reveals spatial tumor heterogeneity in head and neck squamous cell carcinoma. Cancer Lett. 2020 02 28; 471:49-60.
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A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping. Dis Model Mech. 2019 11 04; 13(2).
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c-Myb regulates transcriptional activation of miR-143/145 in vascular smooth muscle cells. PLoS One. 2018; 13(8):e0202778.
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PKC phosphorylates residues in the N-terminal of the DA transporter to regulate amphetamine-induced DA efflux. Neurosci Lett. 2016 05 27; 622:78-82.
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Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant. Am J Hum Genet. 2016 05 05; 98(5):830-842.
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Eradication of Large Solid Tumors by Gene Therapy with a T-Cell Receptor Targeting a Single Cancer-Specific Point Mutation. Clin Cancer Res. 2016 06 01; 22(11):2734-43.
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Elucidation of the Aggregation Pathways of Helix-Turn-Helix Peptides: Stabilization at the Turn Region Is Critical for Fibril Formation. Biochemistry. 2015 Jul 07; 54(26):4050-62.