"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
|
| MeSH Number(s) |
G05.365.590.762.320 G05.558.800.320
|
| 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 |
|---|
| 1994 | 2 | 1 | 3 |
| 1995 | 2 | 6 | 8 |
| 1996 | 4 | 4 | 8 |
| 1997 | 4 | 3 | 7 |
| 1998 | 1 | 4 | 5 |
| 1999 | 0 | 6 | 6 |
| 2000 | 2 | 8 | 10 |
| 2001 | 1 | 6 | 7 |
| 2002 | 1 | 13 | 14 |
| 2003 | 1 | 7 | 8 |
| 2004 | 0 | 6 | 6 |
| 2005 | 3 | 11 | 14 |
| 2006 | 3 | 10 | 13 |
| 2007 | 5 | 9 | 14 |
| 2008 | 4 | 7 | 11 |
| 2009 | 2 | 13 | 15 |
| 2010 | 4 | 10 | 14 |
| 2011 | 2 | 7 | 9 |
| 2012 | 3 | 10 | 13 |
| 2013 | 4 | 12 | 16 |
| 2014 | 1 | 10 | 11 |
| 2015 | 1 | 9 | 10 |
| 2016 | 3 | 8 | 11 |
| 2017 | 1 | 7 | 8 |
| 2018 | 0 | 6 | 6 |
| 2019 | 3 | 8 | 11 |
| 2020 | 1 | 7 | 8 |
| 2021 | 0 | 3 | 3 |
| 2022 | 1 | 0 | 1 |
| 2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Gene Deletion" by people in Profiles.
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MGA deletion leads to Richter's transformation by modulating mitochondrial OXPHOS. Sci Transl Med. 2024 Jul 31; 16(758):eadg7915.
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Uterine Inflammatory Myofibroblastic Tumors: p16 as a Surrogate for CDKN2A Deletion and Predictor of Aggressive Behavior. Am J Surg Pathol. 2024 Jul 01; 48(7):813-824.
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PRDM9 losses in vertebrates are coupled to those of paralogs ZCWPW1 and ZCWPW2. Proc Natl Acad Sci U S A. 2022 03 01; 119(9).
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AUTS2 Regulates RNA Metabolism and Dentate Gyrus Development in Mice. Cereb Cortex. 2021 08 26; 31(10):4808-4824.
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Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey. Mol Genet Genomic Med. 2021 07; 9(7):e1665.
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Robust integration of multiple single-cell RNA sequencing datasets using a single reference space. Nat Biotechnol. 2021 07; 39(7):877-884.
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Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR. Circ Genom Precis Med. 2021 02; 14(1):e003029.
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Fibroblast-enriched endoplasmic reticulum protein TXNDC5 promotes pulmonary fibrosis by augmenting TGFß signaling through TGFBR1 stabilization. Nat Commun. 2020 08 26; 11(1):4254.
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Novel Murine Models of Cerebral Cavernous Malformations. Angiogenesis. 2020 11; 23(4):651-666.
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Distinct Pathways Carry Out a and ß Galactosylation of Secondary Cell Wall Polysaccharide in Bacillus anthracis. J Bacteriol. 2020 07 09; 202(15).