"Turkey" 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 |
D014421
|
MeSH Number(s) |
Z01.252.245.500.850
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Turkey".
Below are MeSH descriptors whose meaning is more specific than "Turkey".
This graph shows the total number of publications written about "Turkey" by people in this website by year, and whether "Turkey" 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 | 0 | 1 | 1 |
2009 | 0 | 2 | 2 |
2010 | 0 | 1 | 1 |
2012 | 0 | 3 | 3 |
2013 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2015 | 0 | 2 | 2 |
2016 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Turkey" by people in Profiles.
-
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Hum Mol Genet. 2017 07 01; 26(13):2577-2588.
-
A novel homozygous mutation in UNC13D presenting as Epstein-Barr-virus-associated lymphoproliferative disease at 9?years of age. Leuk Lymphoma. 2016 12; 57(12):2949-2951.
-
Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability. Hum Mol Genet. 2015 Jul 01; 24(13):3708-17.
-
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. Clin Exp Dermatol. 2015 Oct; 40(7):781-5.
-
Haploidentical stem cell transplantation in DOCK8 deficiency - Successful control of pre-existing severe viremia with a TCRa?/CD19-depleted graft and antiviral treatment. Clin Immunol. 2014 May-Jun; 152(1-2):111-4.
-
Validation of reported genetic risk factors for periodontitis in a large-scale replication study. J Clin Periodontol. 2013 Jun; 40(6):563-72.
-
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair. Exp Dermatol. 2012 Jun; 21(6):469-71.
-
Evaluation of pre- and post-surgical oxidative stress parameters in patients with pulmonary cystic echinococcus. Eur Rev Med Pharmacol Sci. 2012 Apr; 16(4):525-9.
-
A phenotype map for 14q32.3 terminal deletions. Am J Med Genet A. 2012 Apr; 158A(4):695-706.
-
Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation. Am J Med Genet A. 2010 Oct; 152A(10):2628-33.