WebMay 17, 2024 · The question of how dissemination is controlled by SPDEF under the activated NPTNβ has not been answered. Here, we show that the NPTNβ-SPDEF-mediated induction of solute carrier family 22 member 18 antisense (SLC22A18AS) is definitely required for the epithelial-mesenchymal transition (EMT) through the NPTNβ pathway in … WebSLC17A1, solute carrier family 17 member 1. Synonyms NAPI-1, NPT1, NPT-1 Links HGNC:10929. NCBI Gene ID: 6568. neXtProt AC: NX_Q14916. UniProt: Q14916 ... 22 …
Solute carrier family 23 member 2 Sigma-Aldrich
WebSolute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene. Function. Organic ion transporters, such as SLC22A15, transport various medically … WebNov 15, 2024 · Friedreich's ataxia (FRDA) is an autosomal recessive neurodegenerative disease usually caused by large homozygous expansions of GAA repeat sequences in … cinfin agency login
Human Solute carrier family 22 member 18 (SLC22A18) ELISA Kit …
WebMar 21, 2024 · SLC22A17 (Solute Carrier Family 22 Member 17) is a Protein Coding gene. Among its related pathways are Insulin receptor recycling and Transport of inorganic … WebApr 19, 2012 · In affected members of an Iranian family with thiamine-responsive megaloblastic anemia syndrome (TRMA; 249270 ), Diaz et al. (1999) identified a 2-bp deletion involving 429T and 430T of the SLC19A2 gene. Three affected members of the family were studied and found to be homozygous. Two sets of parents and 1 unaffected … WebPolyclonal 22; ... Un-conjugated 17; ... ZnT9 antibody, si:ch211-240l14.4 antibody, zgc:92098 antibody, 2310024J23Rik antibody, AL024256 antibody, solute carrier family 30 member … cinf engineering