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Medical Hypotheses
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February 24, 2012
Self-entanglement of long linear DNA vectors using transient non-B-DNA attachment points: a new concept for improvement of non-viral therapeutic gene delivery
Oleg E Tolmachov
Current Gene Therapy
|
October 26, 2011
Building mosaics of therapeutic plasmid gene vectors
Oleg E Tolmachov
Artificial Intelligence in Medicine
|
December 31, 2014
Self-focusing therapeutic gene delivery with intelligent gene vector swarms: intra-swarm signalling through receptor transgene expression in targeted cells
Oleg E Tolmachov
Medical Hypotheses
|
August 18, 2019
Shielding of non-target cells using RNA vectors conferring gene transfer resistance: A strategy to enhance targeting accuracy and reduce side-effects in therapeutic gene delivery
Oleg E Tolmachov
Medical Hypotheses
|
May 24, 2014
Split vector systems for ultra-targeted gene delivery: a contrivance to achieve ethical assurance of somatic gene therapy in vivo
Oleg E Tolmachov
Medical Hypotheses
|
November 17, 2009
Tightly-wound miniknot vectors for gene therapy: a potential improvement over supercoiled minicircle DNA
Oleg E Tolmachov
Medical Hypotheses
|
August 31, 2015
Transgenic DNA modules with pre-programmed self-destruction: Universal molecular devices to escape 'genetic litter' in gene and cell therapy
Oleg E Tolmachov
Briefings in Bioinformatics
|
December 15, 2020
Novel ChIP-seq simulating program with superior versatility: isChIP
Tatiana Subkhankulova, Fedor Naumenko, Oleg E Tolmachov, et al.
3 Biotech
|
March 22, 2017
Remarkable stability of an instability-prone lentiviral vector plasmid in Escherichia coli Stbl3
Faisal A Al-Allaf, Oleg E Tolmachov, Lia Paola Zambetti, et al.
The Journal of Gene Medicine
|
January 10, 2012
CHM/REP1 cDNA delivery by lentiviral vectors provides functional expression of the transgene in the retinal pigment epithelium of choroideremia mice
Tanya Tolmachova, Oleg E Tolmachov, Silene T Wavre-Shapton, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Medical Hypotheses
|
February 24, 2012
Self-entanglement of long linear DNA vectors using transient non-B-DNA attachment points: a new concept for improvement of non-viral therapeutic gene delivery
Oleg E Tolmachov
Current Gene Therapy
|
October 26, 2011
Building mosaics of therapeutic plasmid gene vectors
Oleg E Tolmachov
Artificial Intelligence in Medicine
|
December 31, 2014
Self-focusing therapeutic gene delivery with intelligent gene vector swarms: intra-swarm signalling through receptor transgene expression in targeted cells
Oleg E Tolmachov
Medical Hypotheses
|
August 18, 2019
Shielding of non-target cells using RNA vectors conferring gene transfer resistance: A strategy to enhance targeting accuracy and reduce side-effects in therapeutic gene delivery
Oleg E Tolmachov
Medical Hypotheses
|
May 24, 2014
Split vector systems for ultra-targeted gene delivery: a contrivance to achieve ethical assurance of somatic gene therapy in vivo
Oleg E Tolmachov
Medical Hypotheses
|
November 17, 2009
Tightly-wound miniknot vectors for gene therapy: a potential improvement over supercoiled minicircle DNA
Oleg E Tolmachov
Medical Hypotheses
|
August 31, 2015
Transgenic DNA modules with pre-programmed self-destruction: Universal molecular devices to escape 'genetic litter' in gene and cell therapy
Oleg E Tolmachov
Briefings in Bioinformatics
|
December 15, 2020
Novel ChIP-seq simulating program with superior versatility: isChIP
Tatiana Subkhankulova, Fedor Naumenko, Oleg E Tolmachov, et al.
3 Biotech
|
March 22, 2017
Remarkable stability of an instability-prone lentiviral vector plasmid in Escherichia coli Stbl3
Faisal A Al-Allaf, Oleg E Tolmachov, Lia Paola Zambetti, et al.
The Journal of Gene Medicine
|
January 10, 2012
CHM/REP1 cDNA delivery by lentiviral vectors provides functional expression of the transgene in the retinal pigment epithelium of choroideremia mice
Tanya Tolmachova, Oleg E Tolmachov, Silene T Wavre-Shapton, et al.
Page
of 2