"Spine" 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.
The spinal or vertebral column.
Descriptor ID |
D013131
|
MeSH Number(s) |
A02.835.232.834
|
Concept/Terms |
Spine- Spine
- Vertebral Column
- Column, Vertebral
- Columns, Vertebral
- Vertebral Columns
- Spinal Column
- Column, Spinal
- Columns, Spinal
- Spinal Columns
|
Below are MeSH descriptors whose meaning is more general than "Spine".
Below are MeSH descriptors whose meaning is more specific than "Spine".
This graph shows the total number of publications written about "Spine" by people in this website by year, and whether "Spine" 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 | 1 | 0 | 1 |
2007 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2019 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Spine" by people in Profiles.
-
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. Birth Defects Res. 2022 06; 114(10):478-486.
-
HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res. 2019 06 01; 111(10):591-597.
-
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome. Am J Hum Genet. 2016 09 01; 99(3):711-719.
-
A comparative analysis of the post-cranial skeleton of fossorial and non-fossorial gymnophthalmid lizards. J Morphol. 2013 Aug; 274(8):845-58.
-
VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol. 2012 Oct; 21(4):191-195.
-
Familial occurrence of the VATER/VACTERL association. Pediatr Surg Int. 2012 Jul; 28(7):725-9.
-
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Res A Clin Mol Teratol. 2010 Sep; 88(9):757-61.
-
Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother? Am J Med Genet A. 2007 Jun 01; 143A(11):1135-42.
-
Imaging in spine and spinal cord malformations. Eur J Radiol. 2004 May; 50(2):177-200.