 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 |
|---|
| 1995 | 1 | 2 | 3 | | 1996 | 0 | 6 | 6 | | 1997 | 1 | 6 | 7 | | 1998 | 0 | 4 | 4 | | 1999 | 0 | 5 | 5 | | 2000 | 1 | 3 | 4 | | 2001 | 0 | 7 | 7 | | 2002 | 0 | 8 | 8 | | 2003 | 1 | 8 | 9 | | 2004 | 0 | 2 | 2 | | 2005 | 1 | 5 | 6 | | 2006 | 0 | 6 | 6 | | 2007 | 1 | 3 | 4 | | 2008 | 2 | 6 | 8 | | 2009 | 3 | 3 | 6 | | 2010 | 2 | 5 | 7 | | 2011 | 7 | 4 | 11 | | 2012 | 1 | 5 | 6 | | 2013 | 4 | 1 | 5 | | 2014 | 3 | 7 | 10 | | 2015 | 1 | 2 | 3 | | 2016 | 1 | 4 | 5 | | 2017 | 1 | 3 | 4 | | 2018 | 1 | 2 | 3 | | 2019 | 1 | 1 | 2 | | 2020 | 0 | 2 | 2 | | 2021 | 0 | 2 | 2 | | 2022 | 0 | 1 | 1 | | 2023 | 0 | 1 | 1 | | 2024 | 0 | 2 | 2 | | 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sequence Deletion" by people in Profiles.
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Cline N, Merlo D, Frater S, Pollock NR, Mayor NP, Turner TR, Walsh L, Vivers S, Norman PJ. The Case of a Missing HLA-B Gene. HLA. 2025 Mar; 105(3):e70114.
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Haviland I, Hector RD, Swanson LC, Verran AS, Sherrill E, Frazier Z, Denny AM, Lucash J, Zhang B, Dubbs HA, Marsh ED, Weisenberg JL, Leonard H, Crippa M, Cogliati F, Russo S, Suter B, Rajaraman R, Percy AK, Schreiber JM, Demarest S, Benke TA, Chopra M, Yu TW, Olson HE. Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder. Am J Med Genet A. 2025 Jan; 197(1):e63843.
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Ander SE, Carpentier KS, Sanders W, Lucas CJ, Jolly AJ, Johnson CN, Hawman DW, Heise MT, Moorman NJ, Morrison TE. A 44-Nucleotide Region in the Chikungunya Virus 3' UTR Dictates Viral Fitness in Disparate Host Cells. Viruses. 2024 05 28; 16(6).
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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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