"Nerve Tissue Proteins" 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.
No definition found.
| Descriptor ID |
D009419
|
| MeSH Number(s) |
D12.776.631
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Nerve Tissue Proteins".
Below are MeSH descriptors whose meaning is more specific than "Nerve Tissue Proteins".
This graph shows the total number of publications written about "Nerve Tissue Proteins" by people in this website by year, and whether "Nerve Tissue Proteins" 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 |
|---|
| 2004 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 0 | 2 | 2 |
| 2008 | 3 | 0 | 3 |
| 2009 | 3 | 1 | 4 |
| 2010 | 5 | 0 | 5 |
| 2011 | 3 | 0 | 3 |
| 2012 | 5 | 2 | 7 |
| 2013 | 6 | 4 | 10 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 3 | 4 |
| 2016 | 4 | 0 | 4 |
| 2017 | 3 | 1 | 4 |
| 2018 | 2 | 3 | 5 |
| 2019 | 2 | 1 | 3 |
| 2020 | 2 | 0 | 2 |
| 2021 | 2 | 1 | 3 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nerve Tissue Proteins" by people in Profiles.
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Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes (Basel). 2022 02 25; 13(3).
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Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Mol Psychiatry. 2022 02; 27(2):1111-1119.
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Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ. Genes (Basel). 2021 05 13; 12(5).
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Epigenome-wide association study of whole blood gene expression in Framingham Heart Study participants provides molecular insight into the potential role of CHRNA5 in cigarette smoking-related lung diseases. Clin Epigenetics. 2021 03 22; 13(1):60.
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Nine newly identified individuals refine the phenotype associated with MYT1L mutations. Am J Med Genet A. 2020 05; 182(5):1021-1031.
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Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. Am J Hum Genet. 2020 02 06; 106(2):246-255.
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Expression of Lhx6 in the adult and developing mouse retina. Gene Expr Patterns. 2019 12; 34:119065.
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Dysregulation of a specific immune-related network of genes biologically defines a subset of schizophrenia. Transl Psychiatry. 2019 05 31; 9(1):156.
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GLI3 repressor but not GLI3 activator is essential for mouse eye patterning and morphogenesis. Dev Biol. 2019 06 15; 450(2):141-154.
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Stroke target identification guided by astrocyte transcriptome analysis. Glia. 2019 04; 67(4):619-633.
MeSH information
