Easy quantitative assessment of genome editing by sequence trace decomposition.
about
The Rise of CRISPR/Cas for Genome Editing in Stem CellsNuclease Target Site Selection for Maximizing On-target Activity and Minimizing Off-target Effects in Genome EditingResources for the design of CRISPR gene editing experimentsETO family protein Mtgr1 mediates Prdm14 functions in stem cell maintenance and primordial germ cell formationBCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesisGenerating Mouse Models Using CRISPR-Cas9-Mediated Genome Editing.Reconstituting development of pancreatic intraepithelial neoplasia from primary human pancreas duct cells.The transcriptional repressor complex FRS7-FRS12 regulates flowering time and growth in Arabidopsis.Frameshift indels introduced by genome editing can lead to in-frame exon skipping.Disabling Cas9 by an anti-CRISPR DNA mimicMultiplex Genome Editing to Generate Universal CAR T Cells Resistant to PD1 Inhibition.Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cells.A versatile system for rapid multiplex genome-edited CAR T cell generationRegulation of Gene Editing Activity Directed by Single-Stranded Oligonucleotides and CRISPR/Cas9 Systems.Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells.Creation of targeted genomic deletions using TALEN or CRISPR/Cas nuclease pairs in one-cell mouse embryos.Genome engineering with CRISPR-Cas9 in the mosquito Aedes aegyptiEfficient CRISPR/Cas9-Mediated Genome Editing in Mice by Zygote Electroporation of Nuclease.Systematic Evaluation of Drosophila CRISPR Tools Reveals Safe and Robust Alternatives to Autonomous Gene Drives in Basic Research.Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9.Death receptor-based enrichment of Cas9-expressing cellsGenome Editing with CRISPR-Cas9: Can It Get Any Better?MLL leukemia induction by genome editing of human CD34+ hematopoietic cells.High-throughput genotyping of CRISPR/Cas9-mediated mutants using fluorescent PCR-capillary gel electrophoresis.Maternal Supply of Cas9 to Zygotes Facilitates the Efficient Generation of Site-Specific Mutant Mouse Models.Synergistic drug combinations for cancer identified in a CRISPR screen for pairwise genetic interactionsCRISPR-STAT: an easy and reliable PCR-based method to evaluate target-specific sgRNA activity.Detection of genome-edited mutant clones by a simple competition-based PCR methodBaculoviral delivery of CRISPR/Cas9 facilitates efficient genome editing in human cellsGeneration of a Collection of Mutant Tomato Lines Using Pooled CRISPR Libraries.Digital detection of endonuclease mediated gene disruption in the HIV provirus.Efficient modification of CCR5 in primary human hematopoietic cells using a megaTAL nuclease and AAV donor template.RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing.Modeling invasive lobular breast carcinoma by CRISPR/Cas9-mediated somatic genome editing of the mammary gland.Targeted positron emission tomography imaging of CXCR4 expression in patients with acute myeloid leukemiaA single double-strand break system reveals repair dynamics and mechanisms in heterochromatin and euchromatin.Analyses of point mutation repair and allelic heterogeneity generated by CRISPR/Cas9 and single-stranded DNA oligonucleotides.Highly Efficient Genome Editing of Murine and Human Hematopoietic Progenitor Cells by CRISPR/Cas9.Prospective functional classification of all possible missense variants in PPARG.GTSE1 tunes microtubule stability for chromosome alignment and segregation by inhibiting the microtubule depolymerase MCAK.
P2860
Q26765852-082981CB-BB71-4026-B099-643309DDDA40Q26770012-CB1BD48C-D9A2-4C7F-9CB1-5A81D85E094CQ26776435-925BDF46-851E-45AB-A35F-14FC7BD9DC91Q28589379-AE0B23F3-A0E9-48FC-B8AF-68F097694D29Q28607483-73132D96-250E-4435-8231-5FCD83B93EF6Q30749378-D62F1F63-60B8-4462-BC8C-CCB2980AC13BQ30841369-6ABA0EFE-1C01-417B-8943-BDFEA8186276Q33705566-F2609240-F0F2-46B0-9824-17B8E65FE2CDQ33751947-43F2BE63-4593-46A6-9A81-4E649A50D5B4Q33898855-09795904-2F30-4DA6-9A4F-8932BB5816E0Q34047618-C6FF9412-CDDC-4D13-AF59-352BBC4DF629Q34047674-44E11229-109E-4E3C-A3B8-7A42E4ABBDCBQ34047977-74BDD7E5-D15A-49B6-8A27-97F6BBB901BEQ34479696-7257F133-1CC2-4FB9-9F29-34A420D99BF9Q34482784-20FDC410-F844-4242-8D6F-4FCEF6AC3657Q35024444-4D3175F2-CC27-4050-9DBC-65D4C0B6FF99Q35374845-2324CD9C-F18C-4869-A37C-80E724B18BEBQ35821035-AB3B5049-349F-4F87-88C1-FF3251BB70A7Q35851906-30071E0A-ADBD-4D4F-9EF5-8D3818769ED7Q35896845-2268D404-3A48-4B11-9E8F-E829203D5A07Q35925498-6DE5DE21-756C-4905-BE93-0E26E05BFEDAQ36025657-48C4BE4A-73E2-4366-A595-0C7B535CE7B2Q36115756-5FCB73DF-807B-424D-8C8F-B3DBD1EA4B77Q36205889-4D9334B2-9E76-4681-93FA-A85CCC453C94Q36247871-489F69C5-707A-4302-9109-E9F9C6829330Q36314597-7334E0B5-9206-4B0A-A08B-3D15762A8D9CQ36370882-88304175-B28A-4FA2-9404-2E36E2C9FB5EQ36394048-6F799B8D-1097-40B1-B1D4-6DD5CC2D7FB5Q36412556-B1EAE71B-10C8-45BB-85F5-5B0B6C5A519AQ36413720-EF3A8E34-DE77-43DD-9F6F-6A8D3A278764Q36528328-19972B53-F1B8-40B4-8BBC-28BBA58F5D99Q36684377-234E6B72-46B9-4F5C-AA16-59F4B1B52F62Q36871074-1F38C4CF-6C75-4796-AE64-45414D992256Q37051766-C5F02F3C-F06C-4FFB-A1CF-681DF3B0B75CQ37140477-45305603-FFC8-4380-8EC8-69EF052F7A8FQ37151375-2A5664E3-9D75-4590-85D8-3E4A6A389366Q37243530-3C243506-FCCF-464D-91E8-E509A9974582Q37381914-BCCF86EF-1F0B-42C3-819A-0FCCC210E3A1Q37461625-23CFF9E1-D85F-429E-BE8C-6C1FBF5E0796Q37488344-CB9595A4-B574-4EFD-B9E6-54184A45F18C
P2860
Easy quantitative assessment of genome editing by sequence trace decomposition.
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Easy quantitative assessment of genome editing by sequence trace decomposition.
@ast
Easy quantitative assessment of genome editing by sequence trace decomposition.
@en
Easy quantitative assessment of genome editing by sequence trace decomposition.
@nl
type
label
Easy quantitative assessment of genome editing by sequence trace decomposition.
@ast
Easy quantitative assessment of genome editing by sequence trace decomposition.
@en
Easy quantitative assessment of genome editing by sequence trace decomposition.
@nl
prefLabel
Easy quantitative assessment of genome editing by sequence trace decomposition.
@ast
Easy quantitative assessment of genome editing by sequence trace decomposition.
@en
Easy quantitative assessment of genome editing by sequence trace decomposition.
@nl
P2860
P356
P1476
Easy quantitative assessment of genome editing by sequence trace decomposition.
@en
P2093
Eva K Brinkman
P2860
P356
10.1093/NAR/GKU936
P407
P577
2014-10-09T00:00:00Z