Pages that link to "Sulfate transporter"

The following pages link to Sulfate transporter:

Showing 4 items.

• Journal Article Tag Suite ‎ (links)
• Sulfate transporter (transclusion) ‎ (links)
• SLC26A2 (redirect page) ‎ (links)
  • Acrodermatitis enteropathica ‎ (links)
  • Choline transporter-like protein 1 ‎ (links)
  • SLC22A18 ‎ (links)
  • UDP-galactose translocator ‎ (links)
  • Very long-chain acyl-CoA synthetase ‎ (links)
  • Chondrogenesis ‎ (links)
  • Sodium-coupled monocarboxylate transporter 2 ‎ (links)
  • Long-chain fatty acid transport protein 4 ‎ (links)
  • Mesomelia ‎ (links)
  • SLC22A25 ‎ (links)
  • SLC2A12 ‎ (links)
  • Zinc transporter ZIP2 ‎ (links)
  • Multidrug and toxin extrusion protein 1 ‎ (links)
  • UDP-xylose and UDP-N-acetylglucosamine transporter ‎ (links)
  • SLC2A6 ‎ (links)
  • Sodium-coupled monocarboxylate transporter 1 ‎ (links)
  • Sodium/hydrogen exchanger 8 ‎ (links)
  • Mitochondrial pyruvate carrier 2 ‎ (links)
  • Solute carrier organic anion transporter family member 4A1 ‎ (links)
  • Adenosine 3'-phospho 5'-phosphosulfate transporter 1 ‎ (links)
  • Anion exchanger family ‎ (links)
  • Multi-antimicrobial extrusion protein ‎ (links)
  • Ion transporter ‎ (links)
  • List of human protein-coding genes 4 ‎ (links)
  • SLC2A9 ‎ (links)
  • Sodium-dependent phosphate transport protein 1 ‎ (links)
  • SLC20A2 ‎ (links)
  • Sulfate transporter ‎ (links)
  • SLC13A2 ‎ (links)
  • Jansen's metaphyseal chondrodysplasia ‎ (links)
  • Metaphyseal dysplasia ‎ (links)
  • Raine syndrome ‎ (links)
  • Testicular microlithiasis ‎ (links)
  • Glucose-6-phosphate exchanger SLC37A1 ‎ (links)
  • MOP flippase ‎ (links)
  • Achondroplasia ‎ (links)
  • Pendrin ‎ (links)
  • Enchondroma ‎ (links)
  • Vesicular monoamine transporter 2 ‎ (links)
  • Crohn's disease ‎ (links)
  • Zinc transporter ZIP10 ‎ (links)
  • SLC17A3 ‎ (links)
  • SLC45A3 ‎ (links)
  • Mitochondrial glycine transporter ‎ (links)
  • Sodium–hydrogen antiporter ‎ (links)
  • Congenital chloride diarrhea ‎ (links)
  • Monocarboxylate transporter 1 ‎ (links)
  • Léri–Weill dyschondrosteosis ‎ (links)
  • Putative sodium-coupled neutral amino acid transporter 10 ‎ (links)
  • GLUT8 ‎ (links)
  • Monocarboxylate transporter 9 ‎ (links)
  • Ammonia transporter ‎ (links)
  • GABA transporter type 2 ‎ (links)
  • Camurati–Engelmann disease ‎ (links)
  • Mitochondrial membrane transport protein ‎ (links)
  • SLC2A7 ‎ (links)
  • Glucose-galactose malabsorption ‎ (links)
  • Sodium/glucose cotransporter 1 ‎ (links)
  • Sodium/glucose cotransporter 2 ‎ (links)
  • SLC41A3 ‎ (links)
  • GLUT5 ‎ (links)
  • Osteodystrophy ‎ (links)
  • Neurotransmitter transporter ‎ (links)
  • Achondroplasia in children ‎ (links)
  • Large neutral amino acids transporter small subunit 1 ‎ (links)
  • Heterodimeric amino-acid transporter ‎ (links)
  • Y+L amino acid transporter 2 ‎ (links)
  • Asc-type amino acid transporter 1 ‎ (links)
  • List of OMIM disorder codes ‎ (links)
  • SLC2A11 ‎ (links)
  • Vesicular glutamate transporter 3 ‎ (links)
  • Norepinephrine transporter ‎ (links)
  • Zinc transporter 1 ‎ (links)
  • Zinc transporter 3 ‎ (links)
  • Fibrochondrogenesis ‎ (links)
  • Monocarboxylate transporter 10 ‎ (links)
  • Hartnup disease ‎ (links)
  • SLC5A4 ‎ (links)
  • Enchondromatosis ‎ (links)
  • Vesicular monoamine transporter 1 ‎ (links)
  • Acetyl-coenzyme A transporter 1 ‎ (links)
  • Osteochondroma ‎ (links)
  • SLC2A13 ‎ (links)
  • SLC2A14 ‎ (links)
  • SLC12A9 ‎ (links)
  • SLC12A8 ‎ (links)
  • Congenital disorder of glycosylation ‎ (links)
  • Plasma membrane monoamine transporter ‎ (links)
  • Mitochondrial folate transporter ‎ (links)
  • SLC26A2 (transclusion) ‎ (links)
  • Sodium- and chloride-dependent betaine transporter ‎ (links)
  • Salla disease ‎ (links)
  • Hypochondrogenesis ‎ (links)
  • Achondrogenesis type 2 ‎ (links)
  • Otospondylomegaepiphyseal dysplasia ‎ (links)
  • Spondyloepiphyseal dysplasia congenita ‎ (links)
  • Osteochondroprogenitor cell ‎ (links)
  • Lysinuric protein intolerance ‎ (links)
  • GLUT2 ‎ (links)
  • Hereditary elliptocytosis ‎ (links)
  • SLC13A5 ‎ (links)
  • Importin α ‎ (links)
  • Thyroid dyshormonogenesis ‎ (links)
  • Antley–Bixler syndrome ‎ (links)
  • Zinc transporter ZIP9 ‎ (links)
  • Zinc transporter protein ‎ (links)
  • Karyopherin ‎ (links)
  • Importin ‎ (links)
  • SPATCCM ‎ (links)
  • SLC22A7 ‎ (links)
  • ABCB8 ‎ (links)
  • SLC22A9 ‎ (links)
  • Multidrug and toxin extrusion protein 2 ‎ (links)
  • Solute carrier organic anion transporter family member 3A1 ‎ (links)
  • Long-chain fatty acid transport protein 1 ‎ (links)
  • SLC25A39 ‎ (links)
  • Electrogenic sodium bicarbonate cotransporter 4 ‎ (links)
  • Cationic amino acid transporter 2 ‎ (links)
  • Cationic amino acid transporter 4 ‎ (links)
  • Tricarboxylate transport protein, mitochondrial ‎ (links)
  • P3 protein ‎ (links)
  • ADP/ATP translocase 4 ‎ (links)
  • Sodium/bile acid cotransporter 7 ‎ (links)
  • Large neutral amino acids transporter small subunit 3 ‎ (links)
  • Sodium/hydrogen exchanger 6 ‎ (links)
  • SLC27A3 ‎ (links)
  • Sodium-dependent phosphate transport protein 2C ‎ (links)
  • Mitochondrial 2-oxodicarboxylate carrier ‎ (links)
  • SLC35F1 ‎ (links)
  • Boomerang dysplasia ‎ (links)
  • SLC25A29 ‎ (links)
  • Osteogenesis imperfecta ‎ (links)
  • GLUT1 ‎ (links)
  • GLUT3 ‎ (links)
  • Adenine nucleotide translocator ‎ (links)
  • Glucose-6-phosphate exchanger SLC37A2 ‎ (links)
  • Glucose transporter ‎ (links)
  • Osteochondrodysplasia ‎ (links)
  • Short rib–polydactyly syndrome ‎ (links)
  • Vesicular acetylcholine transporter ‎ (links)
  • Fanconi–Bickel syndrome ‎ (links)
  • Hyperinsulinemic hypoglycemia ‎ (links)
  • Hereditary multiple exostoses ‎ (links)
  • Template:Solute carrier disorders ‎ (links)
  • Template:Solute carrier family ‎ (links)
  • Template:Osteochondrodysplasia ‎ (links)
  • Category:Solute carrier family ‎ (links)
• English Wikipedia @ Freddythechick:CHECKWIKI/WPC 102 dump ‎ (links)