"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 2 | 3 |
| 2009 | 0 | 9 | 9 |
| 2010 | 0 | 8 | 8 |
| 2011 | 0 | 6 | 6 |
| 2012 | 0 | 4 | 4 |
| 2013 | 0 | 3 | 3 |
| 2014 | 0 | 7 | 7 |
| 2015 | 0 | 5 | 5 |
| 2016 | 1 | 4 | 5 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 4 | 4 |
| 2019 | 2 | 1 | 3 |
| 2020 | 2 | 2 | 4 |
| 2021 | 0 | 2 | 2 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 3 | 4 |
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click here.
Below are the most recent publications written about "Gene Knock-In Techniques" by people in Profiles.
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Multiple beta cell-independent mechanisms drive hypoglycemia in Timothy syndrome. Nat Commun. 2024 Oct 17; 15(1):8980.
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Olfactory deficit and gastrointestinal dysfunction precede motor abnormalities in alpha-Synuclein G51D knock-in mice. Proc Natl Acad Sci U S A. 2024 Sep 24; 121(39):e2406479121.
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Mapping SCA1 regional vulnerabilities reveals neural and skeletal muscle contributions to disease. JCI Insight. 2024 Mar 21; 9(9).
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Generation of a humanized mAce2 and a conditional hACE2 mouse models permissive to SARS-COV-2 infection. Mamm Genome. 2024 Jun; 35(2):113-121.
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Nonsense Variant PRDM16-Q187X Causes Impaired Myocardial Development and TGF-? Signaling Resulting in Noncompaction Cardiomyopathy in Humans and Mice. Circ Heart Fail. 2023 12; 16(12):e010351.
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Differential chromatin binding of the lung lineage transcription factor NKX2-1 resolves opposing murine alveolar cell fates in vivo. Nat Commun. 2021 05 04; 12(1):2509.
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JAK2-V617F and interferon-a induce megakaryocyte-biased stem cells characterized by decreased long-term functionality. Blood. 2021 04 22; 137(16):2139-2151.
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The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model. Cancer Res. 2021 05 01; 81(9):2442-2456.
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Apolipoprotein E4 Reduction with Antisense Oligonucleotides Decreases Neurodegeneration in a Tauopathy Model. Ann Neurol. 2021 05; 89(5):952-966.
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TET2 chemically modifies tRNAs and regulates tRNA fragment levels. Nat Struct Mol Biol. 2021 01; 28(1):62-70.