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  • 1-10 of  160 results for ""DNA Copy Number Variations""

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Academic Journal

Nuclear genetic control of mtDNA copy number and heteroplasmy in humans.

  • Authors : Gupta R; Howard Hughes Medical Institute and Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA. .; Broad Institute of MIT and Harvard, Cambridge, MA, USA. .

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; DNA, Mitochondrial*/DNA, Mitochondrial*/DNA, Mitochondrial*/genetics ; Heteroplasmy*/Heteroplasmy*/Heteroplasmy*/genetics

  • Source: Nature [Nature] 2023 Aug; Vol. 620 (7975), pp. 839-848. Date of Electronic Publication: 2023 Aug 16.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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Academic Journal

Spatially resolved clonal copy number alterations in benign and malignant tissue.

  • Authors : Erickson A; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.; He M

Subjects: Clone Cells*/Clone Cells*/Clone Cells*/metabolism ; Clone Cells*/Clone Cells*/Clone Cells*/pathology ; DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics

  • Source: Nature [Nature] 2022 Aug; Vol. 608 (7922), pp. 360-367. Date of Electronic Publication: 2022 Aug 10.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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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

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Academic Journal

Clonal fitness inferred from time-series modelling of single-cell cancer genomes.

Subjects: DNA Copy Number Variations* ; Drug Resistance, Neoplasm*; Triple Negative Breast Neoplasms/Triple Negative Breast Neoplasms/Triple Negative Breast Neoplasms/*genetics

  • Source: Nature [Nature] 2021 Jul; Vol. 595 (7868), pp. 585-590. Date of Electronic Publication: 2021 Jun 23.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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Report

APP gene copy number changes reflect exogenous contamination.

  • Authors : Kim J; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Subjects: DNA Copy Number Variations*; Gene Dosage

  • Source: Nature [Nature] 2020 Aug; Vol. 584 (7821), pp. E20-E28. Date of Electronic Publication: 2020 Aug 19.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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Editorial & Opinion

Reply to: APP gene copy number changes reflect exogenous contamination.

  • Authors : Lee MH; Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.; Liu CS

Subjects: DNA Copy Number Variations*; Gene Dosage

  • Source: Nature [Nature] 2020 Aug; Vol. 584 (7821), pp. E29-E33. Date of Electronic Publication: 2020 Aug 19.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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Academic Journal

Genome sequencing identifies major causes of severe intellectual disability.

Subjects: DNA copy number variations; SINGLE nucleotide polymorphisms; NUCLEOTIDE sequencing

  • Source: Nature. 7/17/2014, Vol. 511 Issue 7509, p344-347. 4p.

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Academic Journal

Integrating common and rare genetic variation in diverse human populations.

Subjects: DNA Copy Number Variations* ; Genome, Human* ; Polymorphism, Single Nucleotide*

  • Source: Nature [Nature] 2010 Sep 02; Vol. 467 (7311), pp. 52-8.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium:

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Academic Journal

Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity.

  • Authors : Turner KM; Ludwig Institute for Cancer Research, University of California at San Diego, La Jolla, California 92093, USA.; Deshpande V

Subjects: Evolution, Molecular* ; Genetic Heterogeneity* ; Models, Genetic*

  • Source: Nature [Nature] 2017 Mar 02; Vol. 543 (7643), pp. 122-125. Date of Electronic Publication: 2017 Feb 08.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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Academic Journal

Formation of new chromatin domains determines pathogenicity of genomic duplications.

  • Authors : Franke M; Max Planck Institute for Molecular Genetics, RG Development &Disease, 14195 Berlin, Germany.; Institute for Medical and Human Genetics, Charité Universitätsmedizin Berlin, 13353 Berlin, Germany.

Subjects: Chromatin Assembly and Disassembly/Chromatin Assembly and Disassembly/Chromatin Assembly and Disassembly/*genetics ; DNA Copy Number Variations/DNA Copy Number Variations/DNA Copy Number Variations/*genetics ; Disease/Disease/Disease/*genetics Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges

  • Source: Nature [Nature] 2016 Oct 13; Vol. 538 (7624), pp. 265-269. Date of Electronic Publication: 2016 Oct 05.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited

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  • 1-10 of  160 results for ""DNA Copy Number Variations""