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Academic Journal

Cell-Free Urine and Plasma DNA Mutational Analysis Predicts Neoadjuvant Chemotherapy Response and Outcome in Patients with Muscle-Invasive Bladder Cancer.

  • Authors : Christensen E; Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Subjects: Neoadjuvant Therapy*/Neoadjuvant Therapy*/Neoadjuvant Therapy*/adverse effects ; Urinary Bladder Neoplasms*/Urinary Bladder Neoplasms*/Urinary Bladder Neoplasms*/drug therapy ; Urinary Bladder Neoplasms*/Urinary Bladder Neoplasms*/Urinary Bladder Neoplasms*/genetics

  • Source: Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2023 Apr 14; Vol. 29 (8), pp. 1582-1591.Publisher: The Association Country of Publication: United States NLM ID: 9502500 Publication Model: Print Cited Medium: Internet ISSN: 1557-3265

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Cell-Free Urine and Plasma DNA Mutational Analysis Predicts Neoadjuvant Chemotherapy Response and Outcome in Patients with Muscle-Invasive Bladder Cancer

Subjects: Muscles/pathology; Cancer Research; Urinary Bladder Neoplasms/drug therapy

  • Source: Christensen, E, Nordentoft, I, Birkenkamp-Demtroder, K, Elbæk, S K, Lindskrog, S V, Taber, A, Andreasen, T G, Strandgaard, T, Knudsen, M, Lamy, P, Agerbæk, M, Jensen, J B & Dyrskjøt, L 2023, '

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Academic Journal

The origins and functional effects of postzygotic mutations throughout the human life span.

  • Authors : Rockweiler NB; Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.; Ramu A

Subjects: Longevity*/Longevity*/Longevity*/genetics ; Zygote* ; DNA Mutational Analysis*

  • Source: Science (New York, N.Y.) [Science] 2023 Apr 14; Vol. 380 (6641), pp. eabn7113. Date of Electronic Publication: 2023 Apr 14.Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print-Electronic

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Academic Journal

Detection of unintended on-target effects in CRISPR genome editing by DNA donors carrying diagnostic substitutions.

  • Authors : Lackner M; Max Planck Institute for Evolutionary Anthropology, Leipzig, Sachsen 04103, Germany.; Helmbrecht N

Subjects: CRISPR-Cas Systems*/CRISPR-Cas Systems*/CRISPR-Cas Systems*/genetics ; Gene Editing*/Gene Editing*/Gene Editing*/methods ; DNA Mutational Analysis*

  • Source: Nucleic acids research [Nucleic Acids Res] 2023 Mar 21; Vol. 51 (5), pp. e26.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group.

  • Authors : Morak M; Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.; MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.

Subjects: Alternative Splicing* ; Colorectal Neoplasms, Hereditary Nonpolyposis*/Colorectal Neoplasms, Hereditary Nonpolyposis*/Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics ; DNA Mismatch Repair*/DNA Mismatch Repair*/DNA Mismatch Repair*/genetics

  • Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2022 Sep; Vol. 30 (9), pp. 1051-1059. Date of Electronic Publication: 2022 Jun 09.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A quantification method of somatic mutations in normal tissues and their accumulation in pediatric patients with chemotherapy.

  • Authors : Ueda S; Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan, 104-0045.; Department of Pathology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan, 305-8576.

Subjects: DNA Mutational Analysis*/DNA Mutational Analysis*/DNA Mutational Analysis*/methods ; Genome, Human* ; High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/methods

  • Source: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2022 Aug 02; Vol. 119 (31), pp. e2123241119. Date of Electronic Publication: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

AutozygosityMapper: Identification of disease-mutations in consanguineous families.

  • Authors : Steinhaus R; Exploratory Diagnostic Sciences, Berliner Institut für Gesundheitsforschung, Berlin 10117, Germany.; Institut für Medizinische Genetik und Humangenetik, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin 13353, Germany.

Subjects: Consanguinity* ; DNA Mutational Analysis*/DNA Mutational Analysis*/DNA Mutational Analysis*/methods; Humans

  • Source: Nucleic acids research [Nucleic Acids Res] 2022 Jul 05; Vol. 50 (W1), pp. W83-W89.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Signatures of copy number alterations in human cancer.

  • Authors : Steele CD; Research Department of Pathology, Cancer Institute, University College London, London, UK.; Abbasi A

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; DNA Mutational Analysis* ; Neoplasms*/Neoplasms*/Neoplasms*/genetics

  • Source: Nature [Nature] 2022 Jun; Vol. 606 (7916), pp. 984-991. Date of Electronic Publication: 2022 Jun 15.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  69,432 results for ""DNA Mutational Analysis""