"Siblings" 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.
Persons or animals having at least one parent in common. (American College Dictionary, 3d ed)
Descriptor ID |
D035781
|
MeSH Number(s) |
F01.829.263.500.490 I01.880.853.150.500.505 M01.781
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Siblings".
Below are MeSH descriptors whose meaning is more specific than "Siblings".
This graph shows the total number of publications written about "Siblings" by people in this website by year, and whether "Siblings" 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 |
---|
2003 | 0 | 2 | 2 |
2005 | 0 | 1 | 1 |
2007 | 1 | 0 | 1 |
2008 | 0 | 2 | 2 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2013 | 0 | 2 | 2 |
2014 | 0 | 3 | 3 |
2015 | 0 | 2 | 2 |
2016 | 1 | 1 | 2 |
2018 | 0 | 1 | 1 |
2019 | 0 | 5 | 5 |
2020 | 0 | 1 | 1 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Siblings" by people in Profiles.
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Central Role of Sibling Small RNAs NgncR_162 and NgncR_163 in Main Metabolic Pathways of Neisseria gonorrhoeae. mBio. 2023 02 28; 14(1):e0309322.
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The IL-2RG R328X nonsense mutation allows partial STAT-5 phosphorylation and defines a critical region involved in the leaky-SCID phenotype. Clin Exp Immunol. 2020 04; 200(1):61-72.
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Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia. Exp Neurol. 2019 10; 320:112958.
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Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvement. Eur J Med Genet. 2020 Feb; 63(2):103649.
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HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res. 2019 06 01; 111(10):591-597.
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Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis. Sci Rep. 2019 03 14; 9(1):4579.
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PDE10A mutation in two sisters with a hyperkinetic movement disorder - Response to levodopa. Parkinsonism Relat Disord. 2019 06; 63:240-242.
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Novel compound heterozygous and homozygous variants of laminin subunit ?3 gene underlie non-Herlitz junctional epidermolysis bullosa in two paternal half-brothers from Saudi Arabia. Congenit Anom (Kyoto). 2019 May; 59(3):99-101.
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Mesial temporal lobe epilepsy associated with KCNT1 mutation. Seizure. 2017 Feb; 45:181-183.
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Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24. J Clin Immunol. 2016 10; 36(7):684-92.