*  Solute carrier organic anion transporter family, member 2A1 | definition of solute carrier organic anion transporter family,...
Looking for online definition of solute carrier organic anion transporter family, member 2A1 in the Medical Dictionary? solute carrier organic anion transporter family, member 2A1 explanation free. What is solute carrier organic anion transporter family, member 2A1? Meaning of solute carrier organic anion transporter family, member 2A1 medical term. What does solute carrier organic anion transporter family, member 2A1 mean?
  http://medical-dictionary.thefreedictionary.com/solute+carrier+organic+anion+transporter+family%2C+member+2A1
*  Achondrogenesis, type IB - SLC26A2 | Connective Tissue Gene Tests
Achondrogenesis, type IB (ACG1B; MIM 600972) is a lethal condition caused by the diastrophic dysplasia sulfate transporter gene mutations (DTDST/SLC26A2). Affected fetuses are usually in breech position and appear hydropic. The limbs and the trunk are shortened. In contrast to the findings in achondrogenesis, type II (ACG2; MIM 200610), the head is of a normal or near normal size and the fingers and toes are short. The feet and toes are rotated inward, a finding shared with diastrophic dysplasia (DTD; MIM 222600), another disorder caused by DTDST mutations.. Read less ...
  http://ctgt.net/disorder/achondrogenesis-type-ib-slc26a2
*  Gene Expression Literature Summary - MGI
J:223752 Cai T, Yang L, Cai W, Guo S, Yu P, Li J, Hu X, Yan M, Shao Q, Jin Y, Sun ZS, Luo ZJ, Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene. Proc Natl Acad Sci U S A. 2015 Jun 30;112(26):8064-9 ...
  http://www.informatics.jax.org/gxdlit/marker/MGI:88388
*  Frontiers | Disruption of the ammonium transporter AMT1.1 alters basal defenses generating resistance against Pseudomonas...
Disruption of the high-affinity nitrate transporter NRT2.1 activates the priming defence against Pseudomonas syringae, resulting in enhanced resistance. In this study, it is demonstrated that the high-affinity ammonium transporter AMT1.1 is a negative regulator of Arabidopsis defence responses. The T-DNA knockout mutant amt1.1 displays enhanced resistance against Plectosphaerella cucumerina and reduced susceptibility to P. syringae. The impairment of AMT1.1 induces significant metabolic changes in the absence of challenge, suggesting that amt1.1 retains constitutive defence responses. Interestingly, amt1.1 combats pathogens differently depending on the lifestyle of the pathogen. In addition, N starvation enhances the susceptibility of wild type plants and the mutant amt1.1 to P. syringae whereas it has no effect on P. cucumerina resistance. The metabolic changes of amt1.1 against P. syringae are subtler and are restricted to the phenylpropanoid pathway, which correlates ...
  https://www.frontiersin.org/articles/10.3389/fpls.2014.00231/full
*  Plus it
Multidrug resistance-associated protein (MRP) and canalicular multispecific organic anion transporter (cMOAT) are closely related mammalian ATP-binding cassette transporters that export organic anions from cells. Transfection studies have established that MRP confers resistance to natural product cytotoxic agents, and recent evidence suggests the possibility that cMOAT may contribute to cytotoxic drug resistance as well. Based upon the potential importance of these transporters in clinical drug resistance and their important physiological roles in the export of the amphiphilic products of phase I and phase II metabolism, we sought to identify other MRP-related transporters. Using a degenerate PCR approach, we isolated a cDNA that encodes a novel ATP-binding cassette transporter, which we designated MOAT-B. The MOAT-B gene was mapped using ...
  http://cancerres.aacrjournals.org/content/58/13/2741
*  Association of Polymorphisms in the Solute Carrier Organic Anion Transporter Family Member 1B1 Gene with Essential Hypertension...
Lin, R., Wang, X., Zhou, W., Fu, W., Wang, Y., Huang, W. and Jin, L. (2011), Association of Polymorphisms in the Solute Carrier Organic Anion Transporter Family Member 1B1 Gene with Essential Hypertension in the Uyghur Population. Annals of Human Genetics, 75: 305-311. doi: 10.1111/j.1469-1809.2010.00622.x ...
  http://onlinelibrary.wiley.com/doi/10.1111/j.1469-1809.2010.00622.x/suppinfo
*  What are the related genes of Atelosteogenesis type 2? | Atelosteogenesis type 2
Atelosteogenesis type 2 is one of several skeletal disorders caused by mutations in the slc26a2 gene. This gene provides instructions for making a protein that is essential for the normal development of cartilage and for its conversion to bone.
  http://www.onlymyhealth.com/what-related-genes-atelosteogenesis-type-12977602493
*  Anti-NRT1.1 | nitrate transporter 1.1 antibodies
... , AS12 2611, antibody to AtNRT1, Nitrate/chlorate transporter, protein CHLORINA 1, AtNPF6.3, Q05085, AT1G12110
  http://www.agrisera.com/en/artiklar/nrt11-nitrate-transporter-11.html
*  Solute carrier organic anion transporter family member 1B3 - DrugBank
This project is supported by the Canadian Institutes of Health Research (award #111062), Alberta Innovates - Health Solutions, and by The Metabolomics Innovation Centre (TMIC), a nationally-funded research and core facility that supports a wide range of cutting-edge metabolomic studies. TMIC is funded by Genome Alberta, Genome British Columbia, and Genome Canada, a not-for-profit organization that is leading Canada's national genomics strategy with funding from the federal government. Maintenance, support, and commercial licensing is provided by OMx Personal Health Analytics, Inc. Designed by Educe Design & Innovation Inc. ...
  https://www.drugbank.ca/biodb/bio_entities/BE0003659
*  Slco1b2 MGI Mouse Gene Detail - MGI:1351899 - solute carrier organic anion transporter family, member 1b2
View mouse Slco1b2 Chr6:141629518-141686646 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression
  http://www.informatics.jax.org/marker/MGI:1351899
*  Slco1c1 MGI Mouse Gene Detail - MGI:1889679 - solute carrier organic anion transporter family, member 1c1
View mouse Slco1c1 Chr6:141524368-141570177 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression
  http://www.informatics.jax.org/marker/MGI:1889679
*  Effect of SLC26 anion transporter disease-causing mutations on the stability of the homologous STAS domain of E. coli DauA ...
The human solute carrier 26 (SLC26) family of anion transporters consists of ten members that are found in various organs in the body including the stomach, intestine, kidney, thyroid and ear where they transport anions including bicarbonate, chloride and sulfate, typically in an exchange mode. Mutations in these genes cause a plethora of diseases such as diastrophic dysplasia affecting sulfate uptake into chondrocytes (SLC26A2), congenital chloride-losing diarrhoea (SLC26A3) affecting chloride secretion in the intestine and Pendred's syndrome (SLC26A4) resulting in hearing loss. To understand how these mutations affect the structures of the SLC26 membrane proteins and their ability to function properly, 12 human disease-causing mutants from SLC26A2, SLC26A3 and SLC26A4 were introduced into the equivalent sites of the sulfate transporter anti-sigma factor antagonist (STAS) domain of a bacterial homologue ...
  http://www.biochemj.org/content/473/5/615
*  nreC - Oxygen regulatory protein NreC - Staphylococcus aureus (strain Mu50 / ATCC 700699) - nreC gene & protein
Member of the two-component regulatory system NreB/NreC involved in the control of dissimilatory nitrate/nitrite reduction in response to oxygen. Phosphorylated NreC binds to a GC-rich palindromic sequence at the promoters of the nitrate (narGHJI) and nitrite (nir) reductase operons, as well as the putative nitrate transporter gene narT, and activates their expression (By similarity).
  http://www.uniprot.org/uniprot/Q99RN8
*  High affinity sulfate transporter elisa and antibody
Shop High affinity sulfate transporter ELISA Kit, Recombinant Protein and High affinity sulfate transporter Antibody at MyBioSource. Custom ELISA Kit, Recombinant Protein and Antibody are available.
  https://www.mybiosource.com/protein_family.php?root=high-affinity-sulfate-transporter
*  Plus it
Although 2C8dH crystallizes as a dimer, high concentrations of a protein modified by deletion of the signal anchor are required for crystallization, which could result in artifactual dimerization (Schoch et al., 2004). In solution, 2C8dH typically elutes as a dimer from size exclusion columns during purification, and dimerization is concentration-dependent and influenced by fatty acids bound to the dimer interface (Schoch et al., 2004). In this study, we present evidence that 2C8H and native CYP2C8 exist as dimers when bound to natural bacterial and mammalian membranes, respectively. Cross-linking of Cys in either the signal anchor/linker or F-G loop regions resulted in covalently linked dimers of the 2C8 proteins. Considering the reported efficiency of cross-linking, which ranged from 25 to 80% for different Cys pairs in the human erythrocyte anion exchange protein (Taylor et al., 2001), a substantial fraction of CYP2C8 is likely to exist ...
  http://dmd.aspetjournals.org/content/38/11/1976
*  Gene Expression Literature Detail
J:82307 Hulander M, Kiernan AE, Blomqvist SR, Carlsson P, Samuelsson EJ, Johansson BR, Steel KP, Enerback S, Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice. Development. 2003 May;130(9):2013-25 ...
  http://www.informatics.jax.org/gxdlit/key/30485
*  SLCO1A2 Gene - GeneCards | SO1A2 Protein | SO1A2 Antibody
Complete information for SLCO1A2 gene (Protein Coding), Solute Carrier Organic Anion Transporter Family Member 1A2, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium
  http://www.genecards.org/cgi-bin/carddisp.pl?gene=SLCO1A2
*  SLCO2A1 Gene - GeneCards | SO2A1 Protein | SO2A1 Antibody
Complete information for SLCO2A1 gene (Protein Coding), Solute Carrier Organic Anion Transporter Family Member 2A1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium
  http://www.genecards.org/cgi-bin/carddisp.pl?id_type=hgnc&id=10955
*  SLCO1B3 Gene - GeneCards | SO1B3 Protein | SO1B3 Antibody
Complete information for SLCO1B3 gene (Protein Coding), Solute Carrier Organic Anion Transporter Family Member 1B3, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium
  http://www.genecards.org/cgi-bin/carddisp.pl?id_type=hgnc&id=10961
*  anti-SLCO1A2 antibody | GeneTex
SLCO1A2 antibody (solute carrier organic anion transporter family, member 1A2) for ELISA, WB. Anti-SLCO1A2 pAb (GTX87607) is tested in Human samples. 100% Ab-Assurance.
  http://www.genetex.com/SLCO1A2-antibody-GTX87607.html
*  Slco1a1 (house mouse) | Gene Target - PubChem
Gene target information for Slco1a1 - solute carrier organic anion transporter family, member 1a1 (house mouse). Find diseases associated with this biological target and compounds tested against it in bioassay experiments.
  https://pubchem.ncbi.nlm.nih.gov/target/gene/28248
*  Plus it
In this study, we describe transcriptional regulation of the hPDS gene encoding pendrin, a major anion exchanger in the CCD, by UGN, an important modulator of fluid and electrolyte homeostasis. We demonstrate a UGN-induced decrease in both pendrin protein expression (Fig. 2) and pendrin mRNA level (Fig. 3, A and B) in kidneys harvested from mice that were injected with this modulator as well as a UGN-induced reduction in endogenous pendrin mRNA level in renal cells (Fig. 3C). In addition, we demonstrate that UGN decreases hPDS promoter activity in transfected renal cells (Figs. 4 and 5). We show that UGN modulates hPDS promoter activity in large part via a HSE located between nt −1119 and −1115 of the hPDS promoter (Figs. 5 and 6), and we demonstrate that HSF1 likely mediates this UGN-induced modulation (Fig. 7). These findings suggest that pendrin gene expression is subject to HSE/HSF1-mediated transcriptional regulation by UGN.. The renal CCD plays a vital role in ...
  http://ajprenal.physiology.org/content/302/5/F614
*  Choaniki: Sei Naru Protein Densetsu - GameSpot
Find reviews, trailers, release dates, news, screenshots, walkthroughs, and more for Choaniki: Sei Naru Protein Densetsu here on GameSpot.
  https://www.gamespot.com/choaniki-sei-naru-protein-densetsu/
*  Sequence Detail
cdna:known chromosome:VEGA66:18:61192919:61211612:-1 gene:OTTMUSG00000032643 gene_biotype:protein_coding transcript_biotype:protein_coding gene_symbol:Slc26a2 description:solute carrier family 26 (sulfate transporter), member 2 ...
  http://www.informatics.jax.org/sequence/OTTMUST00000081213
*  Antivirotika | Medicína, nemoci, studium na 1. LF UK
Antivirotika jsou extrémně pestrou skupinou léčiv, které nejrůznějšími mechanizmy působí proti virovým částicím. Některé narušují replikaci virové DNA, jiné blokují tvorbu virových částic v postižené buňce, další narušují průnik virů do buňky atp ...
  http://www.stefajir.cz/?q=antivirotika