"Gene Deletion" 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 genetic rearrangement through loss of segments of DNA or RNA, bringing sequences which are normally separated into close proximity. This deletion may be detected using cytogenetic techniques and can also be inferred from the phenotype, indicating a deletion at one specific locus.
Descriptor ID |
D017353
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MeSH Number(s) |
G05.365.590.762.320 G05.558.800.320
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Concept/Terms |
Gene Deletion- Gene Deletion
- Deletion, Gene
- Deletions, Gene
- Gene Deletions
|
Below are MeSH descriptors whose meaning is more general than "Gene Deletion".
Below are MeSH descriptors whose meaning is more specific than "Gene Deletion".
This graph shows the total number of publications written about "Gene Deletion" by people in this website by year, and whether "Gene Deletion" 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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1997 | 0 | 1 | 1 |
1998 | 0 | 1 | 1 |
2000 | 1 | 0 | 1 |
2001 | 0 | 2 | 2 |
2003 | 0 | 1 | 1 |
2004 | 0 | 1 | 1 |
2005 | 1 | 2 | 3 |
2006 | 0 | 1 | 1 |
2007 | 1 | 2 | 3 |
2008 | 0 | 2 | 2 |
2009 | 2 | 1 | 3 |
2010 | 1 | 0 | 1 |
2011 | 1 | 1 | 2 |
2012 | 1 | 3 | 4 |
2013 | 3 | 2 | 5 |
2014 | 2 | 5 | 7 |
2015 | 1 | 4 | 5 |
2016 | 0 | 3 | 3 |
2017 | 1 | 0 | 1 |
2018 | 2 | 0 | 2 |
2020 | 1 | 0 | 1 |
2021 | 1 | 1 | 2 |
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Below are the most recent publications written about "Gene Deletion" by people in Profiles.
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Microglial PD-1 stimulation by astrocytic PD-L1 suppresses neuroinflammation and Alzheimer's disease pathology. EMBO J. 2021 12 15; 40(24):e108662.
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Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes (Basel). 2021 09 20; 12(9).
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Exome sequencing identifies frequent genomic loss of TET1 in IDH-wild-type glioblastoma. Neoplasia. 2020 12; 22(12):800-808.
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Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One. 2018; 13(8):e0202022.
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IKZF1plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia. J Clin Oncol. 2018 04 20; 36(12):1240-1249.
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Identification of causative variants in TXNL4A in Burn-McKeown syndrome and isolated choanal atresia. Eur J Hum Genet. 2017 10; 25(10):1126-1133.
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E4 ligase-specific ubiquitination hubs coordinate DNA double-strand-break repair and apoptosis. Nat Struct Mol Biol. 2016 Nov; 23(11):995-1002.
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MicroRNA-1-associated effects of neuron-specific brain-derived neurotrophic factor gene deletion in dorsal root ganglia. Mol Cell Neurosci. 2016 09; 75:36-43.
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Identification of Gene Mutations and Fusion Genes in Patients with S?zary Syndrome. J Invest Dermatol. 2016 07; 136(7):1490-1499.
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Nuclear Architecture Organized by Rif1 Underpins the Replication-Timing Program. Mol Cell. 2016 Jan 21; 61(2):260-73.