"Tunisia" 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.
A country in northern Africa between ALGERIA and LIBYA. Its capital is Tunis.
| Descriptor ID |
D014416
|
| MeSH Number(s) |
Z01.058.266.887
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Tunisia".
Below are MeSH descriptors whose meaning is more specific than "Tunisia".
This graph shows the total number of publications written about "Tunisia" by people in this website by year, and whether "Tunisia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2007 | 0 | 2 | 2 |
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Below are the most recent publications written about "Tunisia" by people in Profiles.
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Adaptive mutations and replacements of virulence traits in the Escherichia coli O104:H4 outbreak population. PLoS One. 2013; 8(5):e63027.
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Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21. J Hum Genet. 2013 Feb; 58(2):98-101.
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Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation. Gene. 2012 Dec 01; 510(2):102-6.
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Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Ann Hum Genet. 2011 Sep; 75(5):598-604.
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Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia. Ann Hum Genet. 2010 Sep 01; 74(5):399-405.
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Clinical and genetic analysis of two Tunisian otosclerosis families. Am J Med Genet A. 2007 Jul 15; 143A(14):1653-60.
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A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism Relat Disord. 2008; 14(1):77-80.
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Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. Mov Disord. 2007 Jan; 22(1):55-61.
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Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance. Am J Hum Genet. 2000 Jan; 66(1):92-9.
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Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype. Am J Hum Genet. 1997 Jan; 60(1):103-12.