Insertion/deletion-activated frame-shift fluorescence protein is a sensitive reporter for genomic DNA editing
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2164
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Insertion/deletion-activated frame-shift fluorescence protein is a sensitive reporter for genomic DNA editing ; volume:20 ; number:1 ; day:24 ; month:7 ; year:2019 ; pages:1-10 ; date:12.2019
BMC genomics ; 20, Heft 1 (24.7.2019), 1-10, 12.2019
- Creator
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Kumar, Akhilesh
Birnbaum, Michael D.
Moorthy, Balaji T.
Singh, Jayanti
Palovcak, Anna
Patel, Devang M.
Zhang, Fangliang
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1186/s12864-019-5963-z
- URN
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urn:nbn:de:101:1-2019121723292415347979
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 AM CEST
Data provider
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Associated
- Kumar, Akhilesh
- Birnbaum, Michael D.
- Moorthy, Balaji T.
- Singh, Jayanti
- Palovcak, Anna
- Patel, Devang M.
- Zhang, Fangliang
- SpringerLink (Online service)
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Carriers of a novel frame-shift insertion in WNT16a possess elevatedpancreatic expression of TCF7L2
A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibres
Skeletal Editing of Indazoles via Silver-Catalyzed Carbene Insertion
Sex-specific aspects of endogenous retroviral insertion and deletion
Statistical alignment based on fragment insertion and deletion models
Therapeutic gene correction of HBB frameshift CD41-42 (-TCTT) deletion in human hematopoietic stem cells
A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report
Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas
Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion
Insertion-deletion polymorphisms (indels) as genetic markers in natural populations
Fluorescent reporters give new insights into antibiotics-induced nonsense and frameshift mistranslation
Carriers of a novel frame-shift insertion in WNT16a possess elevatedpancreatic expression of TCF7L2
A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibres
Skeletal Editing of Indazoles via Silver-Catalyzed Carbene Insertion
Sex-specific aspects of endogenous retroviral insertion and deletion
Statistical alignment based on fragment insertion and deletion models
Therapeutic gene correction of HBB frameshift CD41-42 (-TCTT) deletion in human hematopoietic stem cells
A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report
Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas
Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion