All articles starting with S
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Slayers Premium (スレイヤーズぷれみあむ)
Slayers Premium (スレイヤーズぷれみあむ) is the fifth Slayers theatrical anime movie, premiered in Japan in December 2001. Unlike the four earlier Lina-and-Naga films, it uses the TV series cast and continuity, following an octopus-language curse in the seaside town Acassi.
Slayr
Slayr (Evan McDonald, born 2007), also Slayer77 or countdragons, is a North Philadelphia rage rap and digicore rapper-producer whose 2025 mixtape Half Blood and 2026 deluxe BloodLuxe brought mainstream attention and a 2026 XXL Freshman selection.
Slayyyter
Slayyyter, real name Catherine Grace Garner (born 1996, Kirkwood, Missouri), is an American electropop and hyperpop singer; her releases include the 2019 mixtape Slayyyter, Starfucker, and the 2026 chart-topping WOR$T GIRL IN AMERICA.
Slazenger
Slazenger, British sporting goods brand founded 1881 by Ralph and Albert Slazenger; Wimbledon official ball supplier since 1902, world's longest-running sports sponsorship; owned by Frasers Group since 2004; sells tennis, cricket, golf, hockey, and swimming gear.
SLB Capturi
SLB Capturi is a carbon capture technology company headquartered in Oslo, Norway, jointly owned by SLB and Aker Carbon Capture since 2024, serving cement and waste-to-energy industries.
SLB OneSubsea
SLB OneSubsea is a subsea production and processing joint venture led by SLB with Aker Solutions and Subsea7, closed in October 2023 and headquartered in Oslo and Houston.
SLBP
SLBP (stem-loop binding protein, HBP, gene 7884) is a metazoan RNA-binding protein that binds the 26-nt stem-loop at the 3' end of replication-dependent histone mRNAs, enabling U7 snRNP-dependent 3' end processing, export, translation, and cell cycle-regulated degradation.
SLC Punk!
SLC Punk! (1998/1999) is James Merendino's semi-autobiographical comedy-drama about Stevo (Matthew Lillard) and Heroin Bob (Michael Goorjian), punks in 1985 Salt Lake City, distinguishing it from other punk films by its Mormon-state setting and cult following.
SLC11A1
SLC11A1 (NRAMP1), gene at 2q35 encoding a macrophage phagolysosomal proton-coupled divalent metal transporter central to innate resistance against Mycobacterium, Salmonella, and Leishmania.
SLC12A2
SLC12A2 (NKCC1, BSC2) is a human gene on chromosome 5q23.3 encoding the ubiquitous Na-K-2Cl cotransporter NKCC1, a bumetanide-inhibited chloride importer; loss-of-function variants cause hearing, brain, and multiorgan disorders.
SLC12A3
SLC12A3 is the human gene encoding the thiazide-sensitive sodium-chloride cotransporter NCC, which reabsorbs salt in the kidney distal tubule, is targeted by thiazide diuretics, and causes Gitelman syndrome when mutated.
SLC16A1
SLC16A1 (MCT1) is a human gene at 1p13.2 encoding monocarboxylate transporter 1, a proton-coupled transporter of lactate, pyruvate, and ketone bodies; loss-of-function variants cause ketoacidosis, promoter mutations cause exercise-induced hyperinsulinism.
SLC16A2
SLC16A2, also called MCT8, is an Xq13.2 gene encoding a 12-transmembrane thyroid hormone transporter; mutations cause X-linked Allan-Herndon-Dudley syndrome with high serum T3 and severe neurological impairment.
SLC16A4
SLC16A4 (MCT5, formerly MCT4) is a human gene at 1p13.3 in the 14-member SLC16 monocarboxylate transporter family; its protein is an orphan transporter of unknown substrates, expressed in kidney, placenta, and colon, linked to West Nile virus resistance.
SLC18A2
SLC18A2 (VMAT2, PKDYS2), gene at 10q25.3 encoding the vesicular monoamine transporter 2, a proton-coupled antiporter loading dopamine, serotonin, norepinephrine, and histamine into synaptic vesicles; biallelic variants cause infantile parkinsonism-dystonia.
SLC19A2
SLC19A2 (THTR-1, thiamine transporter 1) is a human gene on chromosome 1q23.3 encoding a 497-amino-acid, 12-transmembrane high-affinity thiamine transporter; mutations cause thiamine-responsive megaloblastic anemia syndrome with diabetes and deafness.
SLC1A1
SLC1A1 (EAAT3, EAAC1) is a human gene on 9p24.2 encoding a trimeric, sodium-coupled high-affinity glutamate, aspartate, and cysteine transporter; loss-of-function mutations cause dicarboxylic aminoaciduria, and the transporter is a kidney-cancer metabolic target.
SLC1A3
SLC1A3 (EAAT1, GLAST) is a human chromosome 5 gene encoding a glial glutamate transporter and chloride channel; pathogenic variants cause episodic ataxia type 6, migraine, and neuropsychiatric associations.
SLC22A12
SLC22A12 (URAT1) is a human gene on chromosome 11 encoding a renal urate-anion exchanger; loss-of-function mutations cause renal hypouricemia type 1, and the protein is the target of uricosuric gout drugs.
SLC22A2
SLC22A2 (OCT2), human gene at 6q25.3 encoding organic cation transporter 2, a 555-amino-acid electrogenic uniporter in renal proximal tubules that clears cationic drugs such as metformin; key variant rs316019 (Ala270Ser).
SLC22A4
SLC22A4 (OCTN1, ergothioneine transporter ETT) is a human chromosome 5q31.1 gene encoding a polyspecific transporter of organic cations and zwitterions; variants are associated with Crohn's disease and hematologic traits.
SLC22A5
SLC22A5 (solute carrier family 22 member 5; aliases OCTN2, CDSP) is a human gene on chromosome 5q31.1 encoding the sodium-dependent, high-affinity carnitine transporter OCTN2; biallelic pathogenic variants cause autosomal recessive systemic primary carnitine deficiency, treatable with carnitine.
SLC25A13
SLC25A13 (CITRIN, ARALAR2) is a human gene at 7q21.3 encoding citrin, a calcium-binding mitochondrial aspartate-glutamate carrier; biallelic mutations cause autosomal recessive citrin deficiency (CTLN2, NICCD, FTTDCD), prevalent in East Asia.
SLC25A3
SLC25A3, the mitochondrial phosphate carrier (PiC) gene on chromosome 12q23, encodes an inner-membrane transporter of phosphate and copper; mutations cause PiC deficiency with muscle ATP synthesis defects.
SLC25A4
SLC25A4 (ANT1, AAC1) is the heart- and muscle-specific mitochondrial ADP/ATP carrier gene at 4q35.1; its mutations cause dominant progressive external ophthalmoplegia, recessive or dominant mtDNA depletion syndromes, and cardiomyopathy.
SLC26A/SulP transporter
SLC26A/SulP transporters (InterPro IPR001902) are a ubiquitous anion transporter family spanning bacteria to humans; 11 mammalian SLC26 genes, STAS-domain C-termini, roles in sulfate, chloride/bicarbonate transport, and diseases like Pendred syndrome.
SLC26A4
SLC26A4 (formerly PDS), chromosome 7 gene encoding pendrin, an anion exchanger of the inner ear, kidney, and thyroid; biallelic mutations cause Pendred syndrome and DFNB4 hearing loss.
SLC27 fatty acid transport proteins
SLC27 fatty acid transport proteins (FATP1-6, also ACSVL1-6) are integral membrane proteins that mediate long-chain fatty acid uptake and acyl-CoA activation; FATP5 is liver-specific, FATP6 heart-specific, and FATP4 links to restrictive dermopathy.
SLC29A1
SLC29A1 (ENT1, hENT1) is the human equilibrative nucleoside transporter 1 gene on 6p21.1 encoding a 456-aa NBMPR-sensitive carrier that moves nucleosides, nucleoside drugs, and nicotinamide across membranes and defines the Augustine blood group.
SLC2A1
SLC2A1 (GLUT1, P11166) is the human gene encoding the facilitative glucose transporter GLUT1, the main glucose carrier of the blood-brain barrier; heterozygous variants cause treatable GLUT1 deficiency syndrome.