nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A CRISPR Approach for Reactivating Latent HIV-1
|
Lin, Angel |
|
2016 |
24 |
3 |
p. 416-418 3 p. |
artikel |
2 |
A New Induction to the Gene and Cell Therapy Hall Of Fame: Genome Editing
|
Sadelain, Michel |
|
2016 |
24 |
3 |
p. 407-408 2 p. |
artikel |
3 |
A Perspective on the State of Genome Editing
|
Carroll, Dana |
|
2016 |
24 |
3 |
p. 412-413 2 p. |
artikel |
4 |
CRISPR-Cas9 Can Inhibit HIV-1 Replication but NHEJ Repair Facilitates Virus Escape
|
Wang, Gang |
|
2016 |
24 |
3 |
p. 522-526 5 p. |
artikel |
5 |
CRISPR/Cas9 Flexes Its Muscles: In Vivo Somatic Gene Editing for Muscular Dystrophy
|
VandenDriessche, Thierry |
|
2016 |
24 |
3 |
p. 414-416 3 p. |
artikel |
6 |
CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy
|
Himeda, Charis L |
|
2016 |
24 |
3 |
p. 527-535 9 p. |
artikel |
7 |
CRISPR-mediated Activation of Latent HIV-1 Expression
|
Limsirichai, Prajit |
|
2016 |
24 |
3 |
p. 499-507 9 p. |
artikel |
8 |
CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice
|
Xu, Li |
|
2016 |
24 |
3 |
p. 564-569 6 p. |
artikel |
9 |
Current Progress in Therapeutic Gene Editing for Monogenic Diseases
|
Prakash, Versha |
|
2016 |
24 |
3 |
p. 465-474 10 p. |
artikel |
10 |
Engineered Viruses as Genome Editing Devices
|
Chen, Xiaoyu |
|
2016 |
24 |
3 |
p. 447-457 11 p. |
artikel |
11 |
Evaluation of TCR Gene Editing Achieved by TALENs, CRISPR/Cas9, and megaTAL Nucleases
|
Osborn, Mark J |
|
2016 |
24 |
3 |
p. 570-581 12 p. |
artikel |
12 |
Genome-editing Technologies for Gene and Cell Therapy
|
Maeder, Morgan L |
|
2016 |
24 |
3 |
p. 430-446 17 p. |
artikel |
13 |
Genome Engineering Using Adeno-associated Virus: Basic and Clinical Research Applications
|
Gaj, Thomas |
|
2016 |
24 |
3 |
p. 458-464 7 p. |
artikel |
14 |
Genome-wide Profiling Reveals Remarkable Parallels Between Insertion Site Selection Properties of the MLV Retrovirus and the piggyBac Transposon in Primary Human CD4+ T Cells
|
Gogol-Döring, Andreas |
|
2016 |
24 |
3 |
p. 592-606 15 p. |
artikel |
15 |
In This Issue
|
|
|
2016 |
24 |
3 |
p. 410- 1 p. |
artikel |
16 |
In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa
|
Bakondi, Benjamin |
|
2016 |
24 |
3 |
p. 556-563 8 p. |
artikel |
17 |
Multidimensional Genome-wide Analyses Show Accurate FVIII Integration by ZFN in Primary Human Cells
|
Sivalingam, Jaichandran |
|
2016 |
24 |
3 |
p. 607-619 13 p. |
artikel |
18 |
Nuclease Target Site Selection for Maximizing On-target Activity and Minimizing Off-target Effects in Genome Editing
|
Lee, Ciaran M |
|
2016 |
24 |
3 |
p. 475-487 13 p. |
artikel |
19 |
Patent Law and Genome Engineering: A Short Guide to a Rapidly Changing Landscape
|
Cloney, Ross |
|
2016 |
24 |
3 |
p. 419-421 3 p. |
artikel |
20 |
Potent and Targeted Activation of Latent HIV-1 Using the CRISPR/dCas9 Activator Complex
|
Saayman, Sheena M |
|
2016 |
24 |
3 |
p. 488-498 11 p. |
artikel |
21 |
Protein Delivery of an Artificial Transcription Factor Restores Widespread Ube3a Expression in an Angelman Syndrome Mouse Brain
|
Bailus, Barbara J |
|
2016 |
24 |
3 |
p. 548-555 8 p. |
artikel |
22 |
Re-expression of Selected Epigenetically Silenced Candidate Tumor Suppressor Genes in Cervical Cancer by TET2-directed Demethylation
|
Huisman, Christian |
|
2016 |
24 |
3 |
p. 536-547 12 p. |
artikel |
23 |
Research Highlights
|
|
|
2016 |
24 |
3 |
p. 411- 1 p. |
artikel |
24 |
Salient Features of Endonuclease Platforms for Therapeutic Genome Editing
|
Certo, Michael T |
|
2016 |
24 |
3 |
p. 422-429 8 p. |
artikel |
25 |
Silent IL2RG Gene Editing in Human Pluripotent Stem Cells
|
Li, Li B |
|
2016 |
24 |
3 |
p. 582-591 10 p. |
artikel |
26 |
Sleeping Beauty Transposon Vectors in Liver-directed Gene Delivery of LDLR and VLDLR for Gene Therapy of Familial Hypercholesterolemia
|
Turunen, Tytteli A K |
|
2016 |
24 |
3 |
p. 620-635 16 p. |
artikel |
27 |
Specific Reactivation of Latent HIV-1 by dCas9-SunTag-VP64-mediated Guide RNA Targeting the HIV-1 Promoter
|
Ji, Haiyan |
|
2016 |
24 |
3 |
p. 508-521 14 p. |
artikel |
28 |
Streptococcus thermophilus CRISPR-Cas9 Systems Enable Specific Editing of the Human Genome
|
Müller, Maximilian |
|
2016 |
24 |
3 |
p. 636-644 9 p. |
artikel |
29 |
The Neisseria meningitidis CRISPR-Cas9 System Enables Specific Genome Editing in Mammalian Cells
|
Lee, Ciaran M |
|
2016 |
24 |
3 |
p. 645-654 10 p. |
artikel |