 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 |
|---|
| 1994 | 0 | 4 | 4 | | 1995 | 1 | 2 | 3 | | 1996 | 0 | 6 | 6 | | 1997 | 1 | 7 | 8 | | 1998 | 0 | 4 | 4 | | 1999 | 0 | 7 | 7 | | 2000 | 1 | 3 | 4 | | 2001 | 0 | 4 | 4 | | 2002 | 0 | 4 | 4 | | 2003 | 1 | 8 | 9 | | 2004 | 1 | 2 | 3 | | 2005 | 1 | 5 | 6 | | 2006 | 0 | 5 | 5 | | 2007 | 1 | 3 | 4 | | 2008 | 2 | 6 | 8 | | 2009 | 3 | 3 | 6 | | 2010 | 2 | 5 | 7 | | 2011 | 7 | 3 | 10 | | 2012 | 1 | 5 | 6 | | 2013 | 3 | 1 | 4 | | 2014 | 3 | 7 | 10 | | 2015 | 1 | 1 | 2 | | 2016 | 1 | 4 | 5 | | 2017 | 1 | 3 | 4 | | 2018 | 1 | 2 | 3 | | 2019 | 1 | 2 | 3 | | 2020 | 0 | 2 | 2 | | 2021 | 0 | 2 | 2 | | 2022 | 0 | 1 | 1 | | 2023 | 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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Grant MJ, Aredo JV, Starrett JH, Stockhammer P, van Alderwerelt van Rosenburgh IK, Wurtz A, Piper-Valillo AJ, Piotrowska Z, Falcon C, Yu HA, Aggarwal C, Scholes D, Patil T, Nguyen C, Phadke M, Li FY, Neal J, Lemmon MA, Walther Z, Politi K, Goldberg SB. Efficacy of Osimertinib in Patients with Lung Cancer Positive for Uncommon EGFR Exon 19 Deletion Mutations. Clin Cancer Res. 2023 06 01; 29(11):2123-2130.
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Yildiz B?l?kbasi E, Karolak JA, Szafranski P, Gambin T, Willard N, Abman SH, Galambos C, Kinsella JP, Stankiewicz P. High-level gonosomal mosaicism for a pathogenic non-coding CNV deletion of the lung-specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV. Mol Genet Genomic Med. 2022 11; 10(11):e2062.
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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, L?schmann I, Wulf S, Czamara D, Papac-Milicevic N, Strau? 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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Szczesniak LM, Bonzerato CG, Schulman JJ, Bah A, Wojcikiewicz RJH. Bok binds to a largely disordered loop in the coupling domain of type 1 inositol 1,4,5-trisphosphate receptor. Biochem Biophys Res Commun. 2021 05 14; 553:180-186.
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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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Medrano G, Cailleux F, Guan P, Kuruvilla K, Barlow-Anacker AJ, Gosain A. B-lymphocyte-intrinsic and -extrinsic defects in secretory immunoglobulin A production in the neural crest-conditional deletion of endothelin receptor B model of Hirschsprung-associated enterocolitis. FASEB J. 2019 06; 33(6):7615-7624.
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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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