DNA Mutational Analysis

"DNA Mutational Analysis" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Biochemical identification of mutational changes in a nucleotide sequence.

Descriptor ID	D004252
MeSH Number(s)	E05.393.760.700.300
Concept/Terms	DNA Mutational Analysis DNA Mutational Analysis Analysis, DNA Mutational Analyses, DNA Mutational DNA Mutational Analyses Mutational Analyses, DNA Mutational Analysis, DNA

Below are MeSH descriptors whose meaning is more general than "DNA Mutational Analysis".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Sequence Analysis [E05.393.760]
Sequence Analysis, DNA [E05.393.760.700]
DNA Mutational Analysis [E05.393.760.700.300]

Below are MeSH descriptors whose meaning is related to "DNA Mutational Analysis".

Below are MeSH descriptors whose meaning is more specific than "DNA Mutational Analysis".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "DNA Mutational Analysis" by people in this website by year, and whether "DNA Mutational Analysis" was a major or minor topic of these publications.

Bar chart showing 140 publications over 27 distinct years, with a maximum of 11 publications in 2013 and 2016

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	0	4	4
1996	0	3	3
1998	0	1	1
1999	0	1	1
2000	0	1	1
2001	0	7	7
2002	0	6	6
2003	1	5	6
2004	1	2	3
2005	1	5	6
2006	0	3	3
2007	0	8	8
2008	0	3	3
2009	0	6	6
2010	0	6	6
2011	0	3	3
2012	2	4	6
2013	0	11	11
2014	0	8	8
2015	2	8	10
2016	1	10	11
2017	0	5	5
2018	0	7	7
2019	1	6	7
2020	1	3	4
2021	1	1	2
2024	0	2	2

Below are the most recent publications written about "DNA Mutational Analysis" by people in Profiles.

Seddon JM, De D, Grunenkovaite L, Ferrara D. Clinical and Imaging Characteristics of PRPH2 Retinopathies in a Longitudinal Cohort and Diagnostic Implications. Invest Ophthalmol Vis Sci. 2024 Dec 02; 65(14):31.

View in: PubMed
Axelsson J, LeBlanc D, Shojaeisaadi H, Meier MJ, Fitzgerald DM, Nachmanson D, Carlson J, Golubeva A, Higgins J, Smith T, Lo FY, Pilsner R, Williams A, Salk J, Marchetti F, Yauk C. Frequency and spectrum of mutations in human sperm measured using duplex sequencing correlate with trio-based de novo mutation analyses. Sci Rep. 2024 10 08; 14(1):23134.

View in: PubMed
Calvo JA, Fritchman B, Hernandez D, Persky NS, Johannessen CM, Piccioni F, Kelch BA, Cantor SB. Comprehensive Mutational Analysis of the BRCA1-Associated DNA Helicase and Tumor-Suppressor FANCJ/BACH1/BRIP1. Mol Cancer Res. 2021 06; 19(6):1015-1025.

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Mollica V, Franceschini T, Gruppioni E, Rizzo A, Ricci C, Schiavina R, Brunocilla E, Ardizzoni A, Fiorentino M, Giunchi F, Massari F. Broad spectrum mutational analysis of chromophobe renal cell carcinoma using next-generation sequencing. Pathol Res Pract. 2021 Mar; 219:153350.

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Zhu X, Jamshed S, Zou J, Azar A, Meng X, Bathini V, Dresser K, Strock C, Yalamarti B, Yang M, Tomaszewicz K, Tjionas G, Mochel MC, Hutchinson L, Bledsoe JR. Molecular and immunophenotypic characterization of anal squamous cell carcinoma reveals distinct clinicopathologic groups associated with HPV and TP53 mutation status. Mod Pathol. 2021 05; 34(5):1017-1030.

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Klimova AN, Sandler SJ. Mutational Analysis of Residues in PriA and PriC Affecting Their Ability To Interact with SSB in Escherichia coli K-12. J Bacteriol. 2020 11 04; 202(23).

View in: PubMed
Harris T, Sheel A, Zong Y, Hutchinson LM, Cornejo KM, Bubendorf L, Yates J, Fischer AH. Cytologically targeted next-generation sequencing: a synergy for diagnosing urothelial carcinoma. J Am Soc Cytopathol. 2021 Jan-Feb; 10(1):94-102.

View in: PubMed
Bandyopadhyay S, Bhaduri S, ?rd M, Davey NE, Loog M, Pryciak PM. Comprehensive Analysis of G1 Cyclin Docking Motif Sequences that Control CDK Regulatory Potency In?Vivo. Curr Biol. 2020 11 16; 30(22):4454-4466.e5.

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Guan H, Toraldo G, Cerda S, Godley FA, Rao SR, McAneny D, Doherty G, Braverman L, Lee SL. Utilities of RAS Mutations in Preoperative Fine Needle Biopsies for Decision Making for Thyroid Nodule Management: Results from a Single-Center Prospective Cohort. Thyroid. 2020 04; 30(4):536-547.

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Craig JW, Hasserjian RP, Kim AS, Aster JC, Pinkus GS, Hornick JL, Steensma DP, Coleman Lindsley R, DeAngelo DJ, Morgan EA. Detection of the KITD816V mutation in myelodysplastic and/or myeloproliferative neoplasms and acute myeloid leukemia with myelodysplasia-related changes predicts concurrent systemic mastocytosis. Mod Pathol. 2020 06; 33(6):1135-1145.

View in: PubMed

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