"Sequence 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.
Deletion of sequences of nucleic acids from the genetic material of an individual.
| Descriptor ID |
D017384
|
| MeSH Number(s) |
G05.365.590.762 G05.558.800
|
| Concept/Terms |
Sequence Deletion- Sequence Deletion
- Deletion, Sequence
- Deletions, Sequence
- Sequence Deletions
Deletion Mutation- Deletion Mutation
- Deletion Mutations
- Mutation, Deletion
- Mutations, Deletion
|
Below are MeSH descriptors whose meaning is more general than "Sequence Deletion".
Below are MeSH descriptors whose meaning is more specific than "Sequence Deletion".
This graph shows the total number of publications written about "Sequence Deletion" by people in this website by year, and whether "Sequence 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 | 7 | 11 | 18 |
| 1995 | 3 | 19 | 22 |
| 1996 | 5 | 27 | 32 |
| 1997 | 4 | 21 | 25 |
| 1998 | 3 | 19 | 22 |
| 1999 | 3 | 19 | 22 |
| 2000 | 1 | 17 | 18 |
| 2001 | 3 | 11 | 14 |
| 2002 | 3 | 16 | 19 |
| 2003 | 5 | 10 | 15 |
| 2004 | 2 | 10 | 12 |
| 2005 | 5 | 19 | 24 |
| 2006 | 3 | 11 | 14 |
| 2007 | 2 | 9 | 11 |
| 2008 | 4 | 12 | 16 |
| 2009 | 6 | 13 | 19 |
| 2010 | 5 | 15 | 20 |
| 2011 | 3 | 9 | 12 |
| 2012 | 9 | 12 | 21 |
| 2013 | 6 | 15 | 21 |
| 2014 | 4 | 14 | 18 |
| 2015 | 4 | 7 | 11 |
| 2016 | 8 | 8 | 16 |
| 2017 | 3 | 11 | 14 |
| 2018 | 2 | 11 | 13 |
| 2019 | 4 | 8 | 12 |
| 2020 | 0 | 7 | 7 |
| 2021 | 1 | 3 | 4 |
| 2022 | 0 | 8 | 8 |
| 2023 | 0 | 5 | 5 |
| 2024 | 0 | 2 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Sequence Deletion" by people in Profiles.
-
Neurodevelopmental Disorder Caused by Deletion of CHASERR, a lncRNA Gene. N Engl J Med. 2024 Oct 24; 391(16):1511-1518.
-
Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder. Am J Med Genet A. 2025 Jan; 197(1):e63843.
-
"De novo replication repair deficient glioblastoma, IDH-wildtype" is a distinct glioblastoma subtype in adults that may benefit from immune checkpoint blockade. Acta Neuropathol. 2023 12 11; 147(1):3.
-
Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia. Clin Epigenetics. 2023 10 21; 15(1):169.
-
HPV-positive clinically advanced squamous cell carcinoma of the urinary bladder (aBSCC): A comprehensive genomic profiling (CGP) study. Urol Oncol. 2023 12; 41(12):486.e15-486.e23.
-
Common and distinct patterns of acquired uniparental disomy and homozygous deletions between lung squamous cell carcinomas and lung adenocarcinoma. Neoplasia. 2023 11; 45:100932.
-
BAK contributes critically to necrosis and infarct generation during reperfused myocardial infarction. J Mol Cell Cardiol. 2023 11; 184:1-12.
-
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis. Genes (Basel). 2023 02 23; 14(3).
-
Gene dosage changes in KCTD13 result in penile and testicular anomalies via diminished androgen receptor function. FASEB J. 2022 11; 36(11):e22567.
-
Prodrugs of a 1-Hydroxy-2-oxopiperidin-3-yl Phosphonate Enolase Inhibitor for the Treatment of ENO1-Deleted Cancers. J Med Chem. 2022 10 27; 65(20):13813-13832.