| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1080/09687680010028771 |
| P698 | PubMed publication ID | 11396607 |
| P2093 | author name string | Fernández E | |
| Zorzano A | |||
| Chillarón J | |||
| Palacin M | |||
| P2860 | cites work | Cloning and functional expression of a human Na(+) and Cl(-)-dependent neutral and cationic amino acid transporter B(0+) | Q22003724 |
| Identification and characterization of a membrane protein (y+L amino acid transporter-1) that associates with 4F2hc to encode the amino acid transport activity y+L. A candidate gene for lysinuric protein intolerance | Q22008055 | ||
| Cloning and expression of a plasma membrane cystine/glutamate exchange transporter composed of two distinct proteins | Q22009401 | ||
| Identification of a membrane protein, LAT-2, that Co-expresses with 4F2 heavy chain, an L-type amino acid transport activity with broad specificity for small and large zwitterionic amino acids | Q22010207 | ||
| LAT2, a new basolateral 4F2hc/CD98-associated amino acid transporter of kidney and intestine | Q22010848 | ||
| Identification and characterization of a Na(+)-independent neutral amino acid transporter that associates with the 4F2 heavy chain and exhibits substrate selectivity for small neutral D- and L-amino acids | Q22253376 | ||
| Primary structure, genomic organization, and functional and electrogenic characteristics of human system N 1, a Na+- and H+-coupled glutamine transporter | Q22254138 | ||
| Cloning and characterization of a human brain Na(+)-independent transporter for small neutral amino acids that transports D-serine with high affinity | Q22254342 | ||
| Amino-acid transport by heterodimers of 4F2hc/CD98 and members of a permease family | Q24316388 | ||
| Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine | Q24316503 | ||
| Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria | Q24563071 | ||
| Luminal heterodimeric amino acid transporter defective in cystinuria | Q24647174 | ||
| A novel system A isoform mediating Na+/neutral amino acid cotransport | Q28570693 | ||
| Expression cloning and characterization of a transporter for large neutral amino acids activated by the heavy chain of 4F2 antigen (CD98) | Q28570781 | ||
| Molecular analysis of system N suggests novel physiological roles in nitrogen metabolism and synaptic transmission | Q28571345 | ||
| Identification of an amino acid transporter associated with the cystinuria-related type II membrane glycoprotein | Q28573987 | ||
| Cloning of a rat kidney cDNA that stimulates dibasic and neutral amino acid transport and has sequence similarity to glucosidases | Q28582178 | ||
| Amino acid transport system A resembles system N in sequence but differs in mechanism | Q30881347 | ||
| Expression cloning of a cDNA from rabbit kidney cortex that induces a single transport system for cystine and dibasic and neutral amino acids | Q30989726 | ||
| Expression cloning of a Na(+)-independent neutral amino acid transporter from rat kidney | Q33273495 | ||
| New glycoprotein-associated amino acid transporters | Q33777404 | ||
| Surface antigen CD98(4F2): not a single membrane protein, but a family of proteins with multiple functions | Q33833818 | ||
| Cloning and functional identification of a neuronal glutamine transporter | Q33888894 | ||
| Heteromeric amino acid transporters explain inherited aminoacidurias | Q34035393 | ||
| Ultrastructural localization of a neutral and basic amino acid transporter in rat kidney and intestine | Q36489601 | ||
| Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients | Q39366895 | ||
| Structure, expression and regulation of the murine 4F2 heavy chain. | Q40447822 | ||
| Na+-independent lysine transport in human intestinal Caco-2 cells | Q42518757 | ||
| Cystine uptake by rat renal brush-border vesicles | Q42537151 | ||
| Transport interactions of cystine and dibasic amino acids in isolated rat renal tubules | Q42671404 | ||
| Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1. | Q47927198 | ||
| Identification and functional characterization of a Na+-independent neutral amino acid transporter with broad substrate selectivity | Q47951227 | ||
| Cystinuria calls for heteromultimeric amino acid transporters. | Q48933384 | ||
| Expression and insulin-regulated distribution of caveolin in skeletal muscle. Caveolin does not colocalize with GLUT4 in intracellular membranes. | Q51581901 | ||
| On Cystic Oxide, a New Species of Urinary Calculus | Q56038098 | ||
| Functional analysis of mutations in SLC7A9, and genotype–phenotype correlation in non-Type I cystinuria | Q57304635 | ||
| Mutations in the SLC3A1 Gene in Cystinuric Patients: Frequencies and Identification of a Novel Mutation | Q57717361 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 21-26 | |
| P577 | publication date | 2001-01-01 | |
| P1433 | published in | Molecular Membrane Biology | Q6895964 |
| P1476 | title | The amino acid transport system b(o,+) and cystinuria | |
| P478 | volume | 18 |
| Q24316834 | A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter |
| Q90482483 | Amino Acid Transport Across the Mammalian Intestine |
| Q38622499 | Associating mutations causing cystinuria with disease severity with the aim of providing precision medicine. |
| Q39452656 | Compensatory Renal Hypertrophy and the Uptake of Cysteine S-Conjugates of Hg2+ in Isolated S2 Proximal Tubular Segments |
| Q34580141 | Cysteine/cystine redox signaling in cardiovascular disease |
| Q36693550 | Cystine and glutamate transport in renal epithelial cells transfected with human system x(-) (c). |
| Q35021712 | Cystinuria and other noncalcareous calculi |
| Q37979121 | Cystinuria: mechanisms and management |
| Q45314791 | Defective SLC3A1 causes cystinuria (CSNU) |
| Q45316389 | Defective SLC7A9 causes cystinuria (CSNU) |
| Q101215889 | Gallic Acid Affects Intestinal-Epithelial-Cell Integrity and Selected Amino-Acid Uptake in Porcine In-Vitro and Ex-Vivo Permeability Models |
| Q46865472 | Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria |
| Q34435256 | Heteromeric amino acid transporters: biochemistry, genetics, and physiology |
| Q35103270 | Homocysteine, system b0,+ and the renal epithelial transport and toxicity of inorganic mercury |
| Q43954147 | Homologues of amino acid permeases: cloning and tissue expression of XAT1 and XAT2. |
| Q38670021 | Increases in circulating amino acids with in-feed antibiotics correlated with gene expression of intestinal amino acid transporters in piglets |
| Q37139488 | Inherited epithelial transporter disorders--an overview |
| Q34489092 | Kidney stones: pathophysiology and medical management. |
| Q38898368 | Mechanisms involved in the transport of mercuric ions in target tissues |
| Q36983742 | Mercuric conjugates of cysteine are transported by the amino acid transporter system b(0,+): implications of molecular mimicry. |
| Q36104172 | Molecular and ionic mimicry and the transport of toxic metals. |
| Q34123039 | Transport of inorganic mercury and methylmercury in target tissues and organs. |
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