"Gene Knock-In Techniques" 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.
Techniques used to add in exogenous gene sequence such as mutated genes; REPORTER GENES, to study mechanisms of gene expression; or regulatory control sequences, to study effects of temporal changes to GENE EXPRESSION.
| Descriptor ID |
D055879
|
| MeSH Number(s) |
E05.393.335.249
|
| Concept/Terms |
Gene Knock-In Techniques- Gene Knock-In Techniques
- Gene Knock-In Technique
- Knock-In Technique, Gene
- Knock-In Techniques, Gene
- Technique, Gene Knock-In
- Techniques, Gene Knock-In
- Gene Knock-In
- Gene Knock-Ins
- Knock-In, Gene
- Knock-Ins, Gene
- Gene Knock In
- Gene Knock Ins
- In, Gene Knock
- Ins, Gene Knock
- Knock In, Gene
- Knock Ins, Gene
- Gene Knock In Techniques
|
Below are MeSH descriptors whose meaning is more general than "Gene Knock-In Techniques".
Below are MeSH descriptors whose meaning is more specific than "Gene Knock-In Techniques".
This graph shows the total number of publications written about "Gene Knock-In Techniques" by people in this website by year, and whether "Gene Knock-In Techniques" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 4 | 4 |
| 2009 | 0 | 21 | 21 |
| 2010 | 4 | 21 | 25 |
| 2011 | 3 | 23 | 26 |
| 2012 | 1 | 23 | 24 |
| 2013 | 1 | 24 | 25 |
| 2014 | 1 | 22 | 23 |
| 2015 | 1 | 18 | 19 |
| 2016 | 1 | 11 | 12 |
| 2017 | 1 | 8 | 9 |
| 2018 | 0 | 14 | 14 |
| 2019 | 0 | 18 | 18 |
| 2020 | 6 | 21 | 27 |
| 2021 | 1 | 15 | 16 |
| 2022 | 0 | 2 | 2 |
| 2024 | 1 | 6 | 7 |
Below are the most recent publications written about "Gene Knock-In Techniques" by people in Profiles.
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Targeting CD206+ macrophages disrupts the establishment of a key antitumor immune axis. J Exp Med. 2025 Jan 06; 222(1).
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Phosphatidylserine phospholipase A1 enables GPR34-dependent immune cell accumulation in the peritoneal cavity. J Exp Med. 2024 Nov 04; 221(11).
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Influence of Th1 versus Th2 immune bias on viral, pathological, and immunological dynamics in SARS-CoV-2 variant-infected human ACE2 knock-in mice. EBioMedicine. 2024 Oct; 108:105361.
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Establishment and characterization of an hACE2/hTMPRSS2 knock-in mouse model to study SARS-CoV-2. Front Immunol. 2024; 15:1428711.
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Affinity gaps among B cells in germinal centers drive the selection of MPER precursors. Nat Immunol. 2024 Jun; 25(6):1083-1096.
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Sex-specific associations between AD genotype and the microbiome of human amyloid beta knock-in (hAβ-KI) mice. Alzheimers Dement. 2024 07; 20(7):4935-4950.
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Variant-specific in vitro neuronal network phenotypes and drug sensitivity in SCN2A developmental and epileptic encephalopathy. J Neurochem. 2024 Dec; 168(12):3950-3961.
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Non-viral precision T cell receptor replacement for personalized cell therapy. Nature. 2023 03; 615(7953):687-696.
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Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4. Nature. 2022 06; 606(7916):945-952.
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Improving the efficiency of CRISPR-Cas12a-based genome editing with site-specific covalent Cas12a-crRNA conjugates. Mol Cell. 2021 11 18; 81(22):4747-4756.e7.