Solute carrier family 52

WebMar 21, 2024 · SLC52A2 (Solute Carrier Family 52 Member 2) is a Protein Coding gene. Diseases associated with SLC52A2 include Brown-Vialetto-Van Laere Syndrome 2 and … Web52 5 9.6199999999999994E-2 5.8799999999999998E-4 5.47E-3. 87 6 6.9000000000000006E-2 1E-3 8.8900000000000003E-3. 1881 163 ... solute carrier family 3 member 2 [Source:HGNC Symbol;Acc:HGNC:11026] MZT2A SLC20A1 solute carrier family 20 member 1 [Source:HGNC Symbol;Acc:HGNC:10946] CAPRIN2 SMARCE1 SUMO2 …

The solute carrier 6 family of transporters - Bröer - 2012 - Wiley

Web1 day ago · As mentioned above, many of the proteins in the remote sensing and signaling network include well-known multispecific drug transporters of the SLC (solute carrier; eg, OAT and OCT [organic cation transporter]) and ABC (eg, ABCG2 and MRP [multidrug resistance-associated protein]) families and drug-metabolizing enzymes involved in phase … WebMonika Schweigel-Röntgen, Martin Kolisek, in Current Topics in Membranes, 2014. Abstract. The solute carrier family 41 (SLC41) encompasses three members A1, A2, and A3. Based … bk diamond resorts international https://cleanestrooms.com

A “Two-in-One Hit” Model of Shortcut Carcinogenesis in

WebAmong the DEG, there were five solute carriers: Solute carrier family 25 member 36 (SLC25A36), solute carrier family 37 member 1 (SLC37A1), solute carrier family 45 member 3 (SLC45A3), solute carrier family 52 member 3 (SLC52A3), and solute carrier family 6 member 20 (SLC6A20). WebSLC16A2 (solute carrier family 16, member 2 [thyroid hormonetransporter]) (eg, specific thyroid hormone cell transporterdeficiency, Allan-Herndon-Dudley syndrome), full gene sequence 81405-11 BMPR2 (bone morphogenetic protein receptor, type II[serine/threonine kinase]) (eg, heritable pulmonary arterial hypertension), duplication/deletion analysis WebMultiple Choice Quiz daufuskie island ferry co

Multiple Choice Quiz SOLVED:Which statement about …

Category:SOLUTE CARRIER FAMILY 52 (RIBOFLAVIN TRANSPORTER), …

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Solute carrier family 52

Solute carrier family - bionity.com

WebJan 10, 2024 · Aims:The solute carrier family 2 (SLC2) genes are comprised of 14 members which are essential for the maintenance of glucose uptake and survival of tumour cells. This study was performed to investigate the associations of SLC2 family gene expression with mortality in acute myeloid leukemia (AML).Methods:Clinical features and SLC2 family … Websolute carrier family 52 member 3. Normal Function. The SLC52A3 gene (previously called the C20orf54 gene) provides instructions for making a riboflavin transporter protein called …

Solute carrier family 52

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WebMar 21, 2024 · SLC52A1 (Solute Carrier Family 52 Member 1) is a Protein Coding gene. Diseases associated with SLC52A1 include Riboflavin Deficiency and Riboflavin … WebNov 22, 2005 · PTHR12929 SOLUTE CARRIER FAMILY 52 1 hit; Pfam. View protein in Pfam; PF06237 DUF1011 1 hit; MobiDB. Search ...

WebDisclosed herein is a method for treating an Androgen Receptor-Low/Negative (ARlow/-) prostate cancer in a subject in need thereof comprising administering YM155 monobromide [1- (2-Methoxyethyl) -2-methyl-4, 9-dioxo-3- (pyrazin-2-ylmethyl) -4, 9-dihydro-1H-naphtho [2, 3-d] imidazolium bromide], or an analog, derivative, or pharmaceutically acceptable salt … WebMar 29, 2024 · SLC52A2 solute carrier family 52 member 2 Gene ID: 79581, updated on 29-Mar-2024 Gene type: protein coding Also known as: ... Paralogous members of the …

WebMar 1, 2001 · Solute carrier family 52, riboflavin transporter, member 2. Alternative names. Porcine endogenous retrovirus A receptor 1 1 publication (PERV-A receptor 1 1 … WebPR:000032131 solute carrier family 52, riboflavin transporter, member 3 (term hierarchy) InterPro Domains. IPR009357 Solute carrier family 52, riboflavin transporter. Molecular Reagents less. All nucleic 30. cDNA 29. Primer pair 1. Microarray probesets 3. References more. Summaries. All 41. Developmental Gene Expression 5.

WebSolute carrier family. The SoLute Carrier (SLC) group of membrane transport proteins include over 300 members organized into 47 families. [1] The SLC gene nomenclature system was originally proposed by the Human Genome Organization (HUGO) and is the basis for the official HUGO names of the genes that encode these transporters.

Web鈉鉀氯共轉運蛋白(英語: Na +-K +-2Cl-cotransporter 、NKCC、Na +-K+-2Cl-共同轉運體)是一幫助鈉、鉀、氯 離子進行主動運輸進出細胞的蛋白質。 此轉運膜蛋白有兩種變化或等形(isoforms),稱NKCC1或NKCC2。 NKCC1廣泛地分佈在全身;其在分泌液體的器官中具有重要的功能。 。NKCC2則常出現在腎臟裡,可從尿中 ... daufuskie island fishingWebEnter the email address you signed up with and we'll email you a reset link. daufuskie island ferry contractWebMar 29, 2024 · solute carrier family 52, riboflavin transporter, member 3, SLC52A3a, SLC52A3b, riboflavin transporter 2, solute carrier family 52 (riboflavin transporter), … daufuskie island half marathon 2022WebApr 12, 2024 · SLC7A11 and solute carrier family 3 member 2 (SLC3A2) constitute system Xc- together on the cell membrane, which exports glutamate and imports cystine at a 1:1 ratio. Cystine is rapidly transformed into cysteine intracellularly, the rate-limiting amino acid for the synthesis of GSH. daufuskie island ferry ticketsWebNov 12, 2003 · The objective of this work was to design an acyclovir prodrug that would utilize the human apical sodium-dependent bile acid transporter (hASBT) and enhance acyclovir oral bioavailability. Using each chenodeoxycholate, deoxycholate, cholate, and ursodeoxycholate, four bile acid prodrugs of acyclovir were synthesized, where acyclovir … daufuskie island ferry hilton head privateWebZinc transporter 3 (ZnT3) is a member of the solute-linked carrier 30 (SLC 30) zinc transporter family. It is closely linked to the nervous system, where it takes part in the transport of zinc ions from the cytoplasm to the synaptic vesicles. ZnT3 has also been observed in the enteric nervous system (ENS), but its reactions in response to … bkd indianapolis addressWebMar 15, 2024 · Microarray data analysis showed that some ferroptosis genes are associated with HCM, such as ATF3, LPCAT3, and solute carrier family 1 member 5 (SLC1A5) . Diabetic Cardiomyopathy. DCM is a pathophysiological condition caused by diabetes that contributes to HF where the decline of myocardial cell function is an important mediating mechanism . daufuskie island gas golf cart rentals