Transduction, Genetic

"Transduction, Genetic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The transfer of bacterial DNA by phages from an infected bacterium to another bacterium. This also refers to the transfer of genes into eukaryotic cells by viruses. This naturally occurring process is routinely employed as a GENE TRANSFER TECHNIQUE.

Descriptor ID	D014161
MeSH Number(s)	E05.393.350.800 G05.728.850
Concept/Terms	Transduction, Genetic Transduction, Genetic Genetic Transductions Transductions, Genetic Genetic Transduction

Below are MeSH descriptors whose meaning is more general than "Transduction, Genetic".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Gene Transfer Techniques [E05.393.350]
Transduction, Genetic [E05.393.350.800]
Biological Sciences [G]
Genetic Phenomena [G05]
Recombination, Genetic [G05.728]
Transduction, Genetic [G05.728.850]

Below are MeSH descriptors whose meaning is related to "Transduction, Genetic".

Below are MeSH descriptors whose meaning is more specific than "Transduction, Genetic".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Transduction, Genetic" by people in this website by year, and whether "Transduction, Genetic" was a major or minor topic of these publications.

Bar chart showing 154 publications over 28 distinct years, with a maximum of 13 publications in 2002

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1996	1	1	2
1997	1	2	3
2000	2	5	7
2001	1	1	2
2002	8	5	13
2003	1	4	5
2004	4	3	7
2005	3	2	5
2006	1	4	5
2007	1	5	6
2008	2	9	11
2009	2	6	8
2010	2	7	9
2011	0	2	2
2012	2	6	8
2013	2	6	8
2014	3	3	6
2015	3	4	7
2016	2	6	8
2017	3	5	8
2018	3	1	4
2019	5	1	6
2020	1	2	3
2021	2	2	4
2022	0	1	1
2024	1	1	2
2025	1	1	2
2026	2	0	2

Below are the most recent publications written about "Transduction, Genetic" by people in Profiles.

Cui M, Cheng SY, Liang J, McGowan J, Xu M, Xu G, Luo L, Wu J, Harman CD, Jacobson AL, Kapeller LE, Mayes MA, Namkung S, Sharma T, Leland TB, Zhang F, Yip M, Rossmiller B, Xue T, Chen X, Boonying W, Lotun A, Wang D, Su Q, Xie J, Wei Y, Rothstein AM, Gregory-Ksander MS, Komaromy A, Tian B, Lin H, Punzo C, Tai PWL, Gao G. Modification of the VP1u region boosts transduction of adeno-associated virus vectors for ocular gene therapy. Mol Ther. 2026 May 06; 34(5):2781-2800.

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Hoyle B, Bello D, Hill J, Das S, Kim J. Imaged Capillary Isoelectric Focusing (icIEF) Platform for Characterization of Charge Variants of Adeno-Associated Virus (AAV) Capsids and Impact on their Transduction Efficiency. Curr Gene Ther. 2026; 26(2):1-16.

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Hoyle B, Hill J, Bello D. Quantifying the Full-to-Empty Adeno-Associated Virus (AAV) Capsid Ratios and Their Impact on Transduction Efficiency in vitro. AAPS J. 2025 12 17; 28(1):36.

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Walkey CJ, Snow KJ, Bulcha J, Cox AR, Martinez AE, Ljungberg MC, Lanza DG, De Giorgi M, Chuecos MA, Alves-Bezerra M, Suarez CF, Hartig SM, Hilsenbeck SG, Hsu CW, Saville E, Gaitan Y, Duryea J, Hannigan S, Dickinson ME, Mirochnitchenko O, Wang D, Lutz CM, Heaney JD, Gao G, Murray SA, Lagor WR. A comprehensive atlas of AAV tropism in the mouse. Mol Ther. 2025 Mar 05; 33(3):1282-1299.

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Furusho T, Das R, Hakui H, Sairavi A, Adachi K, Galbraith-Liss MS, Rajagopal P, Horikawa M, Luo S, Li L, Yamada K, Andeen N, Dissen GA, Nakai H. Enhancing gene transfer to renal tubules and podocytes by context-dependent selection of AAV capsids. Nat Commun. 2024 12 30; 15(1):10728.

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Cui M, Su Q, Yip M, McGowan J, Punzo C, Gao G, Tai PWL. The AAV2.7m8 capsid packages a higher degree of heterogeneous vector genomes than AAV2. Gene Ther. 2024 09; 31(9-10):489-498.

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Gonzalez TJ, Simon KE, Blondel LO, Fanous MM, Roger AL, Maysonet MS, Devlin GW, Smith TJ, Oh DK, Havlik LP, Castellanos Rivera RM, Piedrahita JA, ElMallah MK, Gersbach CA, Asokan A. Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing. Nat Commun. 2022 10 10; 13(1):5947.

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Ke H, Guay KP, Flotte TR, Gierasch LM, Gershenson A, Hebert DN. Secretion of functional a1-antitrypsin is cell type dependent: Implications for intramuscular delivery for gene therapy. Proc Natl Acad Sci U S A. 2022 08 02; 119(31):e2206103119.

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Yoon DS, Lee KM, Cho S, Ko EA, Kim J, Jung S, Shim JH, Gao G, Park KH, Lee JW. Cellular and Tissue Selectivity of AAV Serotypes for Gene Delivery to Chondrocytes and Cartilage. Int J Med Sci. 2021; 18(15):3353-3360.

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Kondratov O, Kondratova L, Mandel RJ, Coleman K, Savage MA, Gray-Edwards HL, Ness TJ, Rodriguez-Lebron E, Bell RD, Rabinowitz J, Gamlin PD, Zolotukhin S. A comprehensive study of a 29-capsid AAV library in a non-human primate central nervous system. Mol Ther. 2021 09 01; 29(9):2806-2820.

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