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Search results 401 to 416 out of 416 for Has3

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Type Details Score
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Allele
Name: hyaluronan synthase 3; targeted mutation 1.1, Genoway
Allele Type: Targeted
Attribute String: Conditional ready, Humanized sequence, Inserted expressed sequence, Null/knockout
Allele
Name: hyaluronan synthase 3; targeted mutation 1.2, Genoway
Allele Type: Targeted
Attribute String: Null/knockout
Protein Domain
Type: Family
Description: This entry represents the hyaluronan synthase 2 (HAS2), which plays a role in hyaluronan/hyaluronic acid (HA) synthesis []. There are three different, but related hyaluronan synthases - HAS1, HAS2 and HAS3. They are multipass transmembrane enzymes, the active sites of which protrude from the inner face of the plasma membrane. HA is an unbranched disaccharide glucuronic acid/N-acetylglucosamine polymer and is one of the main components of the extracellular matrix []. High level of HA in humans is associated with cancer progression [, ]. In vertebrates, different HA polymer length can trigger different biological responses. High-molecular-mass HA represses mitogenic signalling and has anti-inflammatory properties, while low-molecular-mass HA promotes proliferation and inflammation [, ]. A study of the naked mole rat showed that HAS2 is overexpressed in naked mole rat fibroblasts, while the expression levels of HAS1 and HAS3 are similar between mouse, human and naked mole-rat cells []. HAS2 is responsible for the synthesis of the high-molecular-mass HA (HMM-HA), which triggers ECI (early contact inhibition) via the CD44 receptor and plays a key role in mediating the cancer resistance of the naked mole rat [].
Publication  
First Author: Collum SD
Year: 2019
Journal: Dis Model Mech
Title: Adenosine and hyaluronan promote lung fibrosis and pulmonary hypertension in combined pulmonary fibrosis and emphysema.
Volume: 12
Issue: 5
Publication
First Author: Sukowati CHC
Year: 2019
Journal: Sci Rep
Title: Hyaluronic acid inhibition by 4-methylumbelliferone reduces the expression of cancer stem cells markers during hepatocarcinogenesis.
Volume: 9
Issue: 1
Pages: 4026
Protein
Organism: Mus musculus/domesticus
Length: 552  
Fragment?: false
Publication
First Author: Tian X
Year: 2013
Journal: Nature
Title: High-molecular-mass hyaluronan mediates the cancer resistance of the naked mole rat.
Volume: 499
Issue: 7458
Pages: 346-9
Publication
First Author: Toole BP
Year: 2004
Journal: Nat Rev Cancer
Title: Hyaluronan: from extracellular glue to pericellular cue.
Volume: 4
Issue: 7
Pages: 528-39
Publication
First Author: Lipponen P
Year: 2001
Journal: Eur J Cancer
Title: High stromal hyaluronan level is associated with poor differentiation and metastasis in prostate cancer.
Volume: 37
Issue: 7
Pages: 849-56
Publication
First Author: Kothapalli D
Year: 2007
Journal: J Cell Biol
Title: Hyaluronan and CD44 antagonize mitogen-dependent cyclin D1 expression in mesenchymal cells.
Volume: 176
Issue: 4
Pages: 535-44