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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Butyrophilin-like 2

ss2, BTNL2, Sus1
Encodes AtSS-2 strictosidine synthase. (from NCBI)
Top mentioned proteins: CAN, HAD, ACID, OUT, somatostatin
Papers using ss2 antibodies
Do myoepithelial cells hold the key for breast tumor progression?
O'Hare Michael J et al., In Breast Cancer Research, 2004
... monoclonal ICR-2, Seralab, Leicestershire, UK) and the myoepithelial membrane antigen CD10 (mouse monoclonal CALLA clone SS2/36, DAKO Corporation, Glostrup, Denmark), followed ...
Papers on ss2
Characterization of IgA1 protease as a surface protective antigen of Streptococcus suis serotype 2.
Zhang et al., Wuhan, China. In Microbes Infect, Feb 2016
UNASSIGNED: IgA1 protease of Streptococcus suis serotype 2 (SS2) has been proven to be relative with virulence and immunogenicity, however, its protective efficacy remained to be evaluated.
Enolase of Streptococcus Suis Serotype 2 Enhances Blood-Brain Barrier Permeability by Inducing IL-8 Release.
Lei et al., Changchun, China. In Inflammation, Feb 2016
UNASSIGNED: Streptococcus suis serotype 2 (SS2) is an emerging zoonosis, and meningitis is the most frequent clinical manifestation, but mechanism of its virulent factor, enolase (Eno), is unknown in meningitis.
Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome.
Lokki et al., Helsinki, Finland. In Circ Cardiovasc Genet, Jan 2016
We found a risk haplotype for the disease containing SNPs from BTNL2 and HLA-DRA genes and the HLA-DRB1*01 allele.
Granuloma genes in sarcoidosis: what is new?
Rybicki et al., Detroit, United States. In Curr Opin Pulm Med, Sep 2015
With relevance to granuloma formation, genes involved in apoptotic processes and immune cell activation were further confirmed (ANXA11 and BTNL2) in multiple ethnicities; others were newly identified (XAF1).
Identification of Novel Laminin- and Fibronectin-binding Proteins by Far-Western Blot: Capturing the Adhesins of Streptococcus suis Type 2.
Zhang et al., Nanjing, China. In Front Cell Infect Microbiol, 2014
With this approach, fifteen potential LN-binding proteins and five potential FN-binding proteins were identified from Streptococcus suis serotype 2 (SS2) CW and EC proteins.
Knowledge-based analysis of genetic associations of rheumatoid arthritis to inform studies searching for pleiotropic genes: a literature review and network analysis.
Rao et al., Beijing, China. In Arthritis Res Ther, 2014
RESULTS: In total, we extracted 116 potential functional pleiotropic genes for RA and eight other diseases, including five hub pleiotropic genes, BTNL2, HLA-DRA, NOTCH4, TNXB, and C6orf10, where BTNL2, NOTCH4, and C6orf10 are novel pleiotropic genes identified by our analysis.
Molecular evolution of GPCRs: Somatostatin/urotensin II receptors.
Larhammar et al., Uppsala, Sweden. In J Mol Endocrinol, 2014
Following the 2R event, the vertebrate ancestor is deduced to have possessed three SS (SS1, SS2, and SS5) and six SSTR (SSTR1-6) genes, on the one hand, and four UII (UII, URP, URP1, and URP2) and five UTS2R (UTS2R1-5) genes, on the other hand.
Impact of gene/genome duplications on the evolution of the urotensin II and somatostatin families.
Lihrmann et al., Paris, France. In Gen Comp Endocrinol, 2013
The UII family consists of four paralogous genes called UII, URP, URP1 and URP2 and the SS family is composed of six paralogous genes named SS1, SS2, SS3, SS4, SS5 and SS6.
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Gu et al., Beijing, China. In Nat Genet, 2012
These loci mapped in or near TTC32-WDR35, GUCY1A3, C6orf10-BTNL2 and ATP2B1.
Genetic factors in OA pathogenesis.
Valdes et al., Oxford, United Kingdom. In Bone, 2012
Genomewide association scans (GWAS) in Asians have uncovered a likely role for structural extracellular matrix components (DVWA), and for molecules involved in immune response (HLA class II DQB1 and BTNL2) but these genes are not associated in Caucasian patients.
Association of variants in BAT1-LTA-TNF-BTNL2 genes within 6p21.3 region show graded risk to leprosy in unrelated cohorts of Indian population.
Bamezai et al., New Delhi, India. In Hum Genet, 2012
We unravel the role of unexplored immunologically important genes, BAT1 and BTNL2, and the haplotypes of the significantly associated SNPs therein, to understand susceptibility to the disease, leprosy and its differential severity.
Butyrophilin-like 2 in pulmonary sarcoidosis: a factor for susceptibility and progression?
Drent et al., Maastricht, Netherlands. In Hum Immunol, 2011
The presence of a BTNL2G16071A variant allele almost doubles the risk of progressing to persistent pulmonary sarcoidosis in addition to increasing the risk of developing sarcoidosis.
The BTNL2 A allele variant is frequent in Danish patients with sarcoidosis.
van Overeem Hansen et al., Copenhagen, Denmark. In Clin Respir J, 2011
The BTNL2 A allele variant occurs with a high frequency in Danish patients with sarcoidosis
Large scale replication study of the association between HLA class II/BTNL2 variants and osteoarthritis of the knee in European-descent populations.
Arden et al., London, United Kingdom. In Plos One, 2010
The rs10947262 and rs7775228 variants are not associated with risk of knee osteoarthritis in European descent populations.
Homozygous variant rs2076530 of BTNL2 and familial sarcoidosis.
Devouassoux et al., Lyon, France. In Sarcoidosis Vasc Diffuse Lung Dis, 2009
the absence of a membrane anchored BTNL2 protein may increase genetic susceptibility to sarcoidosis and familial occurrence of the disease.
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.
Duerr et al., Toronto, Canada. In Nat Genet, 2009
Genome-wide significant evidence for association was found in a region spanning BTNL2 to HLA-DQB1 on chromosome 6p21 for ulcerative colitis.
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.
Schreiber et al., Kiel, Germany. In Nat Genet, 2008
The other markers were located in ARPC2 and in the HLA-BTNL2 region.
Sarcoidosis is associated with a truncating splice site mutation in BTNL2.
Schreiber et al., Kiel, Germany. In Nat Genet, 2005
Sarcoidosis is associated with a truncating splice site mutation in BTNL2
Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery.
Hurt et al., Heidelberg, Germany. In Cell, 2004
Here we report the identification of a protein, Sus1, which functions in both transcription and mRNA export.
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