Journal of Genetic Syndromes & Gene Therapy

Journal of Genetic Syndromes & Gene Therapy
Open Access

ISSN: ISSN: 2157-7412

+32 28087017

Citations Report

Citations Report - Journal of Genetic Syndromes & Gene Therapy [186 Articles]

The articles published in Journal of Genetic Syndromes & Gene Therapy have been cited 186 times by eminent researchers all around the world. Following is the list of articles that have cited the articles published in Journal of Genetic Syndromes & Gene Therapy.

Qu W, Wang M, Wu Y, Xu R (2015) Scalable downstream strategies for purification of recombinant adeno-associated virus vectors in light of the properties. Current pharmaceutical biotechnology 16: 684-95.

Liu CL, Ye P, Lin J, Butts CL, Miao CH (2015) Anti-CD20 as the B-cell targeting agent in a combined therapy to modulate anti-factor VIII immune responses in hemophilia A inhibitor mice. Immune responses to AAV vectors, from bench to bedside 30: 70.

Sherman A, Schlachterman A, Cooper M, Merricks EP, Raymer RA, et al. () Portal vein delivery of viral vectors for gene therapy for hemophilia. Gene Correction: Methods and Protocols 2014: 413-426.

Zolotukhin I, Luo D, Gorbatyuk OS, Hoffman BE, Warrington Jr KH, et al. (2013) Improved adeno-associated viral gene transfer to Murine glioma. Journal of genetic syndrome & gene therapy 4.

Mitchell AM, Samulski RJ (2013) Mechanistic insights into the enhancement of adeno-associated virus transduction by proteasome inhibitors. Journal of virology. 87: 13035-13041.

Rogers GL, Herzog RW (2015) Gene therapy for hemophilia. Frontiers in bioscience (Landmark edition) 20: 556.

Wang D, Zhong L, Nahid MA, Gao G (2014) The potential of adeno-associated viral vectors for gene delivery to muscle tissue. Expert opinion on drug delivery 11: 345-64. 

Aleksejeva I (2013) USE OF GENETICALLY MODIFIED ORGANISMS IN FOOD PRODUCTION AND FUTURE CHALLENGES. InEconomic Science for Rural Development Conference Proceedings.

Stueber D, Marvasti-Sitterly M, Fitch K (2012) Cost Benefit Analysis of GMO Corn in Nepal.

Kienle EC Secrets to finding the ideal mate: New insights into parameters that govern successful Adeno-associated virus (AAV) vector evolution (Doctoral dissertation).

Pankajakshan D, Agrawal DK (2013) Clinical and Translational Challenges in Gene Therapy of Cardiovascular Diseases. INTECH Open Access Publisher.

Fuller TD, Spracklen CN, Ryckman KK, Knake LA, Busch TD,et al.  Accepted Article Preview: Published ahead of advance online publication.

Anderson CD, Moisyadi S, Avelar A, Walton CB, Shohet RV (20163). Ultrasound-targeted hepatic delivery of factor IX in hemophiliac mice. Gene therapy.

George LA, Fogarty PF (2016). Gene therapy for hemophilia: past, present and future. InSeminars in hematology  53: 46-54.

Scott DW (2014) Inhibitors–cellular aspects and novel approaches for tolerance. Haemophilia. 20: 80-6.

Rogers GL, Herzog RW (2015) Gene therapy for hemophilia. Frontiers in bioscience (Landmark edition). 20: 556.

Scott DW, Pratt KP, Miao CH (2013) Progress toward inducing immunologic tolerance to factor VIII. Blood 121: 4449-56.

High KH, Nathwani A, Spencer T, Lillicrap D (2014. Current status of haemophilia gene therapy. Haemophilia 20: 43-9.

Mingozzi F, High KA (2013) Immune responses to AAV vectors: overcoming barriers to successful gene therapy. Blood 122: 23-36.

Falsini S, Ciani L, Ristori S, Fortunato A, Arcangeli A (2014) Advances in lipid-based platforms for RNAi therapeutics. J Med Chem 57: 1138-46.

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