"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.
MeSH Number(s)
G05.355.600.800.320
G05.365.590.762.320
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 Harvard Catalyst Profiles by year, and whether "Gene Deletion" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1992 | 7 | 3 | 10 |
1993 | 6 | 15 | 21 |
1994 | 11 | 13 | 24 |
1995 | 10 | 19 | 29 |
1996 | 19 | 28 | 47 |
1997 | 17 | 33 | 50 |
1998 | 17 | 40 | 57 |
1999 | 9 | 33 | 42 |
2000 | 15 | 49 | 64 |
2001 | 10 | 52 | 62 |
2002 | 13 | 65 | 78 |
2003 | 17 | 61 | 78 |
2004 | 14 | 73 | 87 |
2005 | 16 | 69 | 85 |
2006 | 14 | 70 | 84 |
2007 | 16 | 52 | 68 |
2008 | 19 | 79 | 98 |
2009 | 15 | 53 | 68 |
2010 | 17 | 49 | 66 |
2011 | 16 | 54 | 70 |
2012 | 15 | 70 | 85 |
2013 | 21 | 71 | 92 |
2014 | 10 | 66 | 76 |
2015 | 14 | 61 | 75 |
2016 | 12 | 75 | 87 |
2017 | 11 | 55 | 66 |
2018 | 21 | 42 | 63 |
2019 | 18 | 40 | 58 |
2020 | 16 | 27 | 43 |
2021 | 6 | 31 | 37 |
2022 | 0 | 6 | 6 |
Below are the most recent publications written about "Gene Deletion" by people in Profiles.
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Case 8-2022: A 54-Year-Old Woman with Episodes of Swelling. N Engl J Med. 2022 Mar 17; 386(11):1071-1079.
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Metabolic control of adult neural stem cell self-renewal by the mitochondrial protease YME1L. Cell Rep. 2022 02 15; 38(7):110370.
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Vulvar Yolk Sac Tumors Are Somatically Derived SMARCB1 (INI-1)-Deficient Neoplasms. Am J Surg Pathol. 2022 02 01; 46(2):169-178.
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Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. J Clin Endocrinol Metab. 2022 01 18; 107(2):e681-e687.
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The secreted tyrosine kinase VLK is essential for normal platelet activation and thrombus formation. Blood. 2022 01 06; 139(1):104-117.
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Endothelial-Specific Loss of Sphingosine-1-Phosphate Receptor 1 Increases Vascular Permeability and Exacerbates Bleomycin-induced Pulmonary Fibrosis. Am J Respir Cell Mol Biol. 2022 01; 66(1):38-52.
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Genetic research and clinical analysis of ß-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience. J Clin Lab Anal. 2022 Feb; 36(2):e24181.
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MYCL promotes iPSC-like colony formation via MYC Box 0 and 2 domains. Sci Rep. 2021 12 20; 11(1):24254.
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Matrix Gla Protein Levels Are Associated With Arterial Stiffness and Incident Heart Failure With Preserved Ejection Fraction. Arterioscler Thromb Vasc Biol. 2022 02; 42(2):e61-e73.
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Respiratory disturbances and high risk of sudden death in the neonatal connexin-36 knockout mouse. Physiol Rep. 2021 11; 9(21):e15109.