Syntaxin 16

"Syntaxin 16" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A ubiquitously expressed member of the syntaxin subfamily of SNARE proteins that localizes to the GOLGI APPARATUS.

Descriptor ID

D051438

MeSH Number(s)

D12.776.543.512.249.500.500.750

D12.776.543.990.775.500.500.750

Concept/Terms

Syntaxin 16

Below are MeSH descriptors whose meaning is more general than "Syntaxin 16".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Membrane Proteins [D12.776.543]
Membrane Fusion Proteins [D12.776.543.512]
SNARE Proteins [D12.776.543.512.249]
Q-SNARE Proteins [D12.776.543.512.249.500]
Qa-SNARE Proteins [D12.776.543.512.249.500.500]
Syntaxin 16 [D12.776.543.512.249.500.500.750]
Vesicular Transport Proteins [D12.776.543.990]
SNARE Proteins [D12.776.543.990.775]
Q-SNARE Proteins [D12.776.543.990.775.500]
Qa-SNARE Proteins [D12.776.543.990.775.500.500]
Syntaxin 16 [D12.776.543.990.775.500.500.750]

Below are MeSH descriptors whose meaning is related to "Syntaxin 16".

Below are MeSH descriptors whose meaning is more specific than "Syntaxin 16".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Syntaxin 16" by people in Harvard Catalyst Profiles by year, and whether "Syntaxin 16" was a major or minor topic of these publication.

Bar chart showing 10 publications over 10 distinct years, with a maximum of 1 publications in 1999 and 2005 and 2007 and 2010 and 2012 and 2013 and 2015 and 2017 and 2020 and 2022

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1999	0	1	1
2005	0	1	1
2007	1	0	1
2010	0	1	1
2012	1	0	1
2013	0	1	1
2015	0	1	1
2017	1	0	1
2020	1	0	1
2022	1	0	1

Below are the most recent publications written about "Syntaxin 16" by people in Profiles.

Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. J Clin Endocrinol Metab. 2022 01 18; 107(2):e681-e687.

View in: PubMed
Preferential Maternal Transmission of STX16-GNAS Mutations Responsible for Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B): Another Example of Transmission Ratio Distortion. J Bone Miner Res. 2021 04; 36(4):696-703.

View in: PubMed
Early-Onset Obesity: Unrecognized First Evidence for GNAS Mutations and Methylation Changes. J Clin Endocrinol Metab. 2017 08 01; 102(8):2670-2677.

View in: PubMed
Analysis of Multiple Families With Single Individuals Affected by Pseudohypoparathyroidism Type Ib (PHP1B) Reveals Only One Novel Maternally Inherited GNAS Deletion. J Bone Miner Res. 2016 Apr; 31(4):796-805.

View in: PubMed
TSH elevations as the first laboratory evidence for pseudohypoparathyroidism type Ib (PHP-Ib). J Bone Miner Res. 2015 May; 30(5):906-12.

View in: PubMed
Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humans. PLoS One. 2013; 8(10):e77184.

View in: PubMed
De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases. J Clin Endocrinol Metab. 2012 Dec; 97(12):E2314-9.

View in: PubMed
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity. J Hum Genet. 2012 Apr; 57(4):277-9.

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Methylation-specific multiplex-ligation-dependent probe amplification as a rapid molecular diagnostic tool for pseudohypoparathyroidism type 1b. Genet Test Mol Biomarkers. 2010 Feb; 14(1):135-9.

View in: PubMed
GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in platelets. J Clin Endocrinol Metab. 2008 Dec; 93(12):4851-9.

View in: PubMed

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