"Lysosome-Associated Membrane Glycoproteins" 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.
Ubiquitously expressed integral membrane glycoproteins found in the LYSOSOME.
| Descriptor ID |
D051907
|
| MeSH Number(s) |
D12.776.395.550.550 D12.776.543.550.527
|
| Concept/Terms |
Lysosome-Associated Membrane Glycoproteins- Lysosome-Associated Membrane Glycoproteins
- Lysosome Associated Membrane Glycoproteins
- Membrane Glycoproteins, Lysosome-Associated
- Lysosomal Membrane Proteins
- Membrane Proteins, Lysosomal
Lysosomal-Associated Membrane Proteins- Lysosomal-Associated Membrane Proteins
- Lysosomal Associated Membrane Proteins
- Lysosome-Associated Membrane Proteins
- Lysosome Associated Membrane Proteins
- LAMP Proteins
|
Below are MeSH descriptors whose meaning is more general than "Lysosome-Associated Membrane Glycoproteins".
Below are MeSH descriptors whose meaning is more specific than "Lysosome-Associated Membrane Glycoproteins".
This graph shows the total number of publications written about "Lysosome-Associated Membrane Glycoproteins" by people in this website by year, and whether "Lysosome-Associated Membrane Glycoproteins" 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 |
|---|
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Lysosome-Associated Membrane Glycoproteins" by people in Profiles.
-
Single-nephron proteomes connect morphology and function in proteinuric kidney disease. Kidney Int. 2018 06; 93(6):1308-1319.
-
Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. Am J Hum Genet. 2013 Jul 11; 93(1):181-90.
-
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism. Nat Genet. 2012 Oct; 44(10):1152-5.
-
Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurol. 2011 Oct 27; 11:134.
MeSH information
