 Sequence Deletion
"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
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| MeSH Number(s) |
G05.365.590.762 G05.558.800
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| Concept/Terms |
Sequence Deletion- Sequence Deletion
- Deletion, Sequence
- Deletions, Sequence
- Sequence Deletions
Deletion Mutation- Deletion Mutation
- Deletion Mutations
- Mutation, Deletion
- Mutations, Deletion
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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 |
|---|
| 1992 | 0 | 1 | 1 | | 1994 | 0 | 6 | 6 | | 1995 | 1 | 2 | 3 | | 1996 | 0 | 6 | 6 | | 1997 | 1 | 10 | 11 | | 1998 | 0 | 4 | 4 | | 1999 | 0 | 8 | 8 | | 2000 | 0 | 4 | 4 | | 2001 | 0 | 8 | 8 | | 2002 | 0 | 8 | 8 | | 2003 | 1 | 8 | 9 | | 2004 | 2 | 3 | 5 | | 2005 | 1 | 5 | 6 | | 2006 | 1 | 6 | 7 | | 2007 | 1 | 4 | 5 | | 2008 | 2 | 6 | 8 | | 2009 | 4 | 3 | 7 | | 2010 | 2 | 5 | 7 | | 2011 | 7 | 3 | 10 | | 2012 | 1 | 6 | 7 | | 2013 | 3 | 1 | 4 | | 2014 | 2 | 7 | 9 | | 2015 | 1 | 2 | 3 | | 2016 | 1 | 3 | 4 | | 2017 | 2 | 1 | 3 | | 2018 | 2 | 2 | 4 | | 2019 | 0 | 2 | 2 | | 2020 | 0 | 2 | 2 | | 2021 | 0 | 1 | 1 | | 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sequence Deletion" by people in Profiles.
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Tsai JW, Lee JC, Hsieh TH, Huang SC, Lee PH, Liu TT, Kao YC, Chang CD, Weng TF, Li CF, Lin JC, Liang CW, Su YL, Chang IY, Wang YT, Chang NY, Yu SC, Wang JC, Huang HY. Adult NTRK-rearranged spindle cell neoplasms of the viscera: with an emphasis on rare locations and heterologous elements. Mod Pathol. 2022 07; 35(7):911-921.
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Irmscher S, Zipfel SLH, Halder LD, Ivanov L, Gonzalez-Delgado A, Waldeyer C, Seiffert M, Brunner FJ, von der Heide M, Löschmann I, Wulf S, Czamara D, Papac-Milicevic N, Strauß O, Lorkowski S, Reichenspurner H, Holers MV, Banda NK, Zeller T, Binder EB, Binder CJ, Wiech T, Zipfel PF, Skerka C. Factor H-related protein 1 (FHR-1) is associated with atherosclerotic cardiovascular disease. Sci Rep. 2021 11 18; 11(1):22511.
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Haber G, Conway KM, Paramsothy P, Roy A, Rogers H, Ling X, Kozauer N, Street N, Romitti PA, Fox DJ, Phan HC, Matthews D, Ciafaloni E, Oleszek J, James KA, Galindo M, Whitehead N, Johnson N, Butterfield RJ, Pandya S, Venkatesh S, Bhattaram VA. Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy. Muscle Nerve. 2021 02; 63(2):181-191.
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Holmes ZE, Hamilton DJ, Hwang T, Parsonnet NV, Rinn JL, Wuttke DS, Batey RT. The Sox2 transcription factor binds RNA. Nat Commun. 2020 04 14; 11(1):1805.
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Osso LA, Chan JR. A surprising role for myelin in Williams syndrome. Nat Neurosci. 2019 05; 22(5):681-683.
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Zapf RL, Wiemels RE, Keogh RA, Holzschu DL, Howell KM, Trzeciak E, Caillet AR, King KA, Selhorst SA, Naldrett MJ, Bose JL, Carroll RK. The Small RNA Teg41 Regulates Expression of the Alpha Phenol-Soluble Modulins and Is Required for Virulence in Staphylococcus aureus. mBio. 2019 02 05; 10(1).
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Thompson AC, Capellini TD, Guenther CA, Chan YF, Infante CR, Menke DB, Kingsley DM. A novel enhancer near the Pitx1 gene influences development and evolution of pelvic appendages in vertebrates. Elife. 2018 11 30; 7.
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Snijders Blok L, Hiatt SM, Bowling KM, Prokop JW, Engel KL, Cochran JN, Bebin EM, Bijlsma EK, Ruivenkamp CAL, Terhal P, Simon MEH, Smith R, Hurst JA, McLaughlin H, Person R, Crunk A, Wangler MF, Streff H, Symonds JD, Zuberi SM, Elliott KS, Sanders VR, Masunga A, Hopkin RJ, Dubbs HA, Ortiz-Gonzalez XR, Pfundt R, Brunner HG, Fisher SE, Kleefstra T, Cooper GM. De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder. Hum Genet. 2018 May; 137(5):375-388.
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Hicks EA, Zaveri M, Deschamps PA, Noseworthy MD, Ball A, Williams T, West-Mays JA. Conditional Deletion of AP-2a and AP-2ß in the Developing Murine Retina Leads to Altered Amacrine Cell Mosaics and Disrupted Visual Function. Invest Ophthalmol Vis Sci. 2018 05 01; 59(6):2229-2239.
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Barutcu AR, Maass PG, Lewandowski JP, Weiner CL, Rinn JL. A TAD boundary is preserved upon deletion of the CTCF-rich Firre locus. Nat Commun. 2018 04 13; 9(1):1444.
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