"Wnt1 Protein" 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.
A proto-oncogene protein and member of the Wnt family of proteins. It is expressed in the caudal MIDBRAIN and is essential for proper development of the entire mid-/hindbrain region.
| Descriptor ID |
D051155
|
| MeSH Number(s) |
D12.776.467.984.100 D12.776.624.664.700.967 D23.529.984.100
|
| Concept/Terms |
Wnt1 Protein- Wnt1 Protein
- Wnt1 Proto-Oncogene Protein
- Proto-Oncogene Protein, Wnt1
- Wnt1 Proto Oncogene Protein
- Proto-Oncogene Protein Wnt-1
- Proto Oncogene Protein Wnt 1
- Wnt-1, Proto-Oncogene Protein
- Wnt-1 Protein
- Wnt 1 Protein
- c-int Protein
- Proto-Oncogene Protein Int-1
- Int-1, Proto-Oncogene Protein
- Proto Oncogene Protein Int 1
|
Below are MeSH descriptors whose meaning is more general than "Wnt1 Protein".
Below are MeSH descriptors whose meaning is more specific than "Wnt1 Protein".
This graph shows the total number of publications written about "Wnt1 Protein" by people in this website by year, and whether "Wnt1 Protein" 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 |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 0 | 1 | 1 |
| 1997 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 3 | 3 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2008 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Wnt1 Protein" by people in Profiles.
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Deletion of tetraspanin CD151 alters the Wnt oncogene-induced mammary tumorigenesis: A cell type-linked function and signaling. Neoplasia. 2019 12; 21(12):1151-1163.
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cis-regulatory architecture of a short-range EGFR organizing center in the Drosophila melanogaster leg. PLoS Genet. 2018 08; 14(8):e1007568.
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Human mutations in integrator complex subunits link transcriptome integrity to brain development. PLoS Genet. 2017 May; 13(5):e1006809.
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Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations. J Med Genet. 2016 06; 53(6):427-30.
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Destabilization of heterologous proteins mediated by the GSK3ß phosphorylation domain of the ß-catenin protein. Cell Physiol Biochem. 2013; 32(5):1187-99.
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HMGA2/TET1/HOXA9 signaling pathway regulates breast cancer growth and metastasis. Proc Natl Acad Sci U S A. 2013 Jun 11; 110(24):9920-5.
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Shh and Gli3 regulate formation of the telencephalic-diencephalic junction and suppress an isthmus-like signaling source in the forebrain. Dev Biol. 2011 Nov 15; 359(2):242-50.
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MUCing around with tumor suppression. Cancer Biol Ther. 2008 Dec; 7(12):1968-9.
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Wingless signaling directly regulates cyclin E expression in proliferating embryonic PNS precursor cells. Mech Dev. 2008 Sep-Oct; 125(9-10):857-64.
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WNT1 and WNT3a promote expansion of melanocytes through distinct modes of action. Pigment Cell Res. 2005 Jun; 18(3):167-80.