Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells. - Wikidata - awgldk - TriplyDB

Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells.

Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells.

http://www.wikidata.org/entity/Q34452056

about

CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes Spermatogonial stem cell autotransplantation and germline genomic editing: a future cure for spermatogenic failure and prevention of transmission of genomic diseases Customizing the genome as therapy for the β-hemoglobinopathies The Rise of CRISPR/Cas for Genome Editing in Stem Cells Long-term dual-color tracking of genomic loci by modified sgRNAs of the CRISPR/Cas9 system.CRISPR-Cas9 delivery to hard-to-transfect cells via membrane deformation Genome editing: the road of CRISPR/Cas9 from bench to clinic Epigenetic Memory Underlies Cell-Autonomous Heterogeneous Behavior of Hematopoietic Stem Cells Human Germline CRISPR-Cas Modification: Toward a Regulatory Framework.Applications of CRISPR-Cas9 mediated genome engineering.Regenerative medicine: targeted genome editing in vivo.Targeted Germline Modifications in Rats Using CRISPR/Cas9 and Spermatogonial Stem Cells Generation of fertile offspring from Kit(w)/Kit(wv) mice through differentiation of gene corrected nuclear transfer embryonic stem cells.Efficient inversions and duplications of mammalian regulatory DNA elements and gene clusters by CRISPR/Cas9.CRISPR-Cas9-mediated genome editing and guide RNA design.Introducing precise genetic modifications into human 3PN embryos by CRISPR/Cas-mediated genome editing.Dynamic Heterogeneity of Brachyury in Mouse Epiblast Stem Cells Mediates Distinct Response to Extrinsic Bone Morphogenetic Protein (BMP) Signaling.CRISPR-Cas9: a promising tool for gene editing on induced pluripotent stem cells.Optimization of the production of knock-in alleles by CRISPR/Cas9 microinjection into the mouse zygote.CRISPR-Cas9: a new and promising player in gene therapy.Application of CRISPR/Cas9 genome editing to the study and treatment of disease.High-Throughput Silencing Using the CRISPR-Cas9 System: A Review of the Benefits and Challenges.CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy.Long-Term Propagation of Porcine Undifferentiated Spermatogonia.Plant-pathogen interactions: toward development of next-generation disease-resistant plants.Genome engineering through CRISPR/Cas9 technology in the human germline and pluripotent stem cells.The discovery and development of the CRISPR system in applications in genome manipulation.Modern Genome Editing Technologies in Huntington's Disease Research.Applications of CRISPR/Cas9 in retinal degenerative diseases Overview of CRISPR-Cas9 Biology.Use of Stirred Suspension Bioreactors for Male Germ Cell Enrichment.Leapfrogging: primordial germ cell transplantation permits recovery of CRISPR/Cas9-induced mutations in essential genes Transfer of a Mouse Artificial Chromosome into Spermatogonial Stem Cells Generates Transchromosomic Mice.Genome Editing in Mouse Spermatogonial Stem Cell Lines Using TALEN and Double-Nicking CRISPR/Cas9.Sanofi-Cell Research outstanding paper award of 2015.Advances, challenges and future directions for stem cell therapy in amyotrophic lateral sclerosis.The Future of CRISPR Applications in the Lab, the Clinic and Society.CRISPR-Cas9-Mediated Gene Editing in Mouse Spermatogonial Stem Cells.The Potential of iPSCs for the Treatment of Premature Aging Disorders.Melatonin promotes development of haploid germ cells from early developing spermatogenic cells of Suffolk sheep under in vitro condition.

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P2860

Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells.

http://www.wikidata.org/entity/Q34452056

description

2014 nî lūn-bûn

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2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Correction of a genetic diseas ...... use spermatogonial stem cells.

@ast

Correction of a genetic diseas ...... use spermatogonial stem cells.

@en

Correction of a genetic diseas ...... use spermatogonial stem cells.

@nl

type

label

Correction of a genetic diseas ...... use spermatogonial stem cells.

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Correction of a genetic diseas ...... use spermatogonial stem cells.

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Correction of a genetic diseas ...... use spermatogonial stem cells.

@nl

prefLabel

Correction of a genetic diseas ...... use spermatogonial stem cells.

@ast

Correction of a genetic diseas ...... use spermatogonial stem cells.

@en

Correction of a genetic diseas ...... use spermatogonial stem cells.

@nl

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Correction of a genetic diseas ...... use spermatogonial stem cells.

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Chikai Zhou

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Chunlian Wu

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Dan Liang

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Fuchou Tang

http://www.w3.org/2001/XMLSchema#string

Hai Zhou

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Hong Pan

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Hongshan Guo

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Huijuan Shi

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Jiaoyang Liao

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Jinsong Li

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P2860

Azoospermia in patients heterozygous for a mutation in SYCP3

Germline transmission of donor haplotype following spermatogonial transplantation

RNA-guided human genome engineering via Cas9

Heritable genome editing in C. elegans via a CRISPR-Cas9 system.

Evolution of the mutation rate

Multiplex genome engineering using CRISPR/Cas systems

The germline stem cell niche unit in mammalian testes

Germline stem cells: toward the regeneration of spermatogenesis

Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients

X chromosome-linked muscular dystrophy (mdx) in the mouse

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10.1038/CR.2014.160

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