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Academic Journal

A rapid bioanalytical tool for detection of sequence-specific circular DNA and mitochondrial DNA point mutations.

  • Authors : Zhang Y; Department of Electrical Engineering and Computer Science, University of Cincinnati, Cincinnati, OH, 45221, USA.; Kaynak A

Subjects: Point Mutation*; DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*instrumentation ; DNA, Circular/DNA, Circular/DNA, Circular/*genetics

  • Source: Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2019 Apr; Vol. 411 (10), pp. 1935-1941. Date of Electronic Publication: 2019 Feb 27.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101134327 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene.

Subjects: Point Mutation*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; NADH Dehydrogenase/NADH Dehydrogenase/NADH Dehydrogenase/*genetics

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2021 Aug; Vol. 42 (4), pp. 440-445. Date of Electronic Publication: 2021 Apr 16.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations.

  • Authors : Coussa RG; Department of Ophthalmology and Visual Sciences, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.; Sohn EH

Subjects: Point Mutation*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*genetics

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2021 Aug; Vol. 42 (4), pp. 420-430. Date of Electronic Publication: 2021 Apr 08.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Leber's Hereditary Optic Neuropathy with visual recovery caused by two rare mutations.

  • Authors : Kisilevsky E; Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada.; Margolin EA

Subjects: Point Mutation*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*genetics

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2021 Aug; Vol. 42 (4), pp. 500-502. Date of Electronic Publication: 2021 May 07.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

De novo mutational signature discovery in tumor genomes using SparseSignatures.

  • Authors : Lal A; Department of Pathology, Stanford University, Stanford, California, United States of America.; Liu K

Subjects: Point Mutation*; DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*statistics & numerical data ; Neoplasms/Neoplasms/Neoplasms/*genetics

  • Source: PLoS computational biology [PLoS Comput Biol] 2021 Jun 28; Vol. 17 (6), pp. e1009119. Date of Electronic Publication: 2021 Jun 28 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101238922 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

An enzymatic on/off switch-mediated assay for KRAS hotspot point mutation detection of circulating tumor DNA.

  • Authors : Wang QL; Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences, Soochow University, Suzhou, China.; Zhou CL

Subjects: Circulating Tumor DNA/Circulating Tumor DNA/Circulating Tumor DNA/*genetics ; Colorectal Neoplasms/Colorectal Neoplasms/Colorectal Neoplasms/*diagnosis ; Point Mutation/Point Mutation/Point Mutation/*genetics

  • Source: Journal of clinical laboratory analysis [J Clin Lab Anal] 2020 Aug; Vol. 34 (8), pp. e23305. Date of Electronic Publication: 2020 Mar 24.Publisher: Wiley Country of Publication: United States NLM ID: 8801384 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-2825

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Academic Journal

Validation of the T86I mutation in the gyrA gene as a highly reliable real time PCR target to detect Fluoroquinolone-resistant Campylobacter jejuni.

  • Authors : Espinoza N; Bacteriology Department, U.S Naval Medical Research Unit-6 (NAMRU-6), Avenida Venezuela, Cuadra 36, Callao, Peru. .; Rojas J

Subjects: Point Mutation*; Campylobacter Infections/Campylobacter Infections/Campylobacter Infections/*diagnosis ; Campylobacter jejuni/Campylobacter jejuni/Campylobacter jejuni/*genetics

  • Source: BMC infectious diseases [BMC Infect Dis] 2020 Jul 16; Vol. 20 (1), pp. 518. Date of Electronic Publication: 2020 Jul 16.Publisher: BioMed Central Country of Publication: England NLM ID: 100968551 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2334

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Academic Journal

Individualized Mutation Detection in Circulating Tumor DNA for Monitoring Colorectal Tumor Burden Using a Cancer-Associated Gene Sequencing Panel.

  • Authors : Sato KA; Molecular Therapeutics Laboratory, Department of Surgery, Iwate Medical University School of Medicine, Morioka, Japan.; Department of Surgery, Iwate medical University School of Medicine, Morioka, Japan.

Subjects: DNA Mutational Analysis* ; Genes, Neoplasm* ; Point Mutation*

  • Source: PloS one [PLoS One] 2016 Jan 04; Vol. 11 (1), pp. e0146275. Date of Electronic Publication: 2016 Jan 04 (Print Publication: 2016).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Pan-cancer analysis of somatic mutations and epigenetic alterations in insulated neighbourhood boundaries.

Subjects: Point Mutation*; CCCTC-Binding Factor/CCCTC-Binding Factor/CCCTC-Binding Factor/*genetics ; CCCTC-Binding Factor/CCCTC-Binding Factor/CCCTC-Binding Factor/*metabolism

  • Source: PloS one [PLoS One] 2020 Jan 16; Vol. 15 (1), pp. e0227180. Date of Electronic Publication: 2020 Jan 16 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

A random mutation capture assay to detect genomic point mutations in mouse tissue.

  • Authors : Wright JH; Department of Pathology, University of Washington and Department of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. ; Modjeski KL

Subjects: DNA Mutational Analysis* ; Point Mutation*; Animals

  • Source: Nucleic acids research [Nucleic Acids Res] 2011 Jun; Vol. 39 (11), pp. e73. Date of Electronic Publication: 2011 Apr 01.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  3,075 results for ""DNA Mutational Analysis""