solute carrier family 19 member 2 ; Homo sapiens






116 Article(s)
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1 3461030 Liposomes as drug carriers for oral ulcers. J Dent Res 1986 Sep 3
2 8423781 Differential regulation of two distinct families of glucose transporter genes in Trypanosoma brucei. Mol Cell Biol 1993 Feb 3
3 9399900 Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping. Am J Hum Genet 1997 Dec 3
4 9856490 Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity. Hum Genet 1998 Oct 3
5 10066388 Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23. Mol Genet Metab 1999 Mar 1
6 10074490 Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts. J Clin Invest 1999 Mar 7
7 10391221 Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nat Genet 1999 Jul 5
8 10391222 The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. Nat Genet 1999 Jul 12
9 10391223 Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. Nat Genet 1999 Jul 5
10 10874303 The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families. Hum Mutat 2000 3
11 10964259 Thiamine intestinal transport and related issues: recent aspects. Proc Soc Exp Biol Med 2000 Sep 3
12 10978358 A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I. J Med Genet 2000 Sep 2
13 11135496 Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy. Ophthalmic Genet 2000 Dec 3
14 11286512 Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians. Mol Genet Metab 2001 Apr 2
15 11358373 Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport. Blood Cells Mol Dis 2001 Jan-Feb 2
16 11380424 A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome. Br J Haematol 2001 May 2
17 11386850 Slc19a2: cloning and characterization of the murine thiamin transporter cDNA and genomic sequence, the orthologue of the human TRMA gene. Mol Genet Metab 2001 Jun 1
18 11592824 Characterization of a murine high-affinity thiamine transporter, Slc19a2. Mol Genet Metab 2001 Sep-Oct 1
19 11731220 SLC19A3 encodes a second thiamine transporter ThTr2. Biochim Biophys Acta 2001 Nov 29 2
20 11997118 Expression and promoter analysis of SLC19A2 in the human intestine. Biochim Biophys Acta 2002 Apr 12 1
21 12065289 Functional role of specific amino acid residues in human thiamine transporter SLC19A2: mutational analysis. Am J Physiol Gastrointest Liver Physiol 2002 Jul 5
22 12435857 Lack of plasma membrane targeting of a G172D mutant thiamine transporter derived from Rogers syndrome family. Mol Med 2002 Aug 4
23 12454006 Cell biology of the human thiamine transporter-1 (hTHTR1). Intracellular trafficking and membrane targeting mechanisms. J Biol Chem 2003 Feb 7 6
24 12488043 Cellular and molecular aspects of thiamin uptake by human liver cells: studies with cultured HepG2 cells. Biochim Biophys Acta 2002 Dec 23 1
25 12643751 Specific association of thiamine-coated gadolinium nanoparticles with human breast cancer cells expressing thiamine transporters. Bioconjug Chem 2003 Mar-Apr 1
26 12900388 In vitro and in vivo characterization of the minimal promoter region of the human thiamin transporter SLC19A2. Am J Physiol Cell Physiol 2003 Sep 1
27 14615284 Expression and functional contribution of hTHTR-2 in thiamin absorption in human intestine. Am J Physiol Gastrointest Liver Physiol 2004 Mar 2
28 14622275 Disruption of transport activity in a D93H mutant thiamine transporter 1, from a Rogers Syndrome family. Eur J Biochem 2003 Nov 3
29 14627317 Cardiac manifestations in thiamine-responsive megaloblastic anemia syndrome. Pediatr Cardiol 2003 Sep-Oct 1
30 14770311 SLC19: the folate/thiamine transporter family. Pflugers Arch 2004 Feb 1
31 14994241 Novel mutation in the SLC19A2 gene in an African-American female with thiamine-responsive megaloblastic anemia syndrome. Am J Med Genet A 2004 Mar 15 1
32 15016149 TRMA syndrome (thiamine-responsive megaloblastic anemia): a case report and review of the literature. Pediatr Diabetes 2002 Dec 2
33 15337749 Restoration of transport activity by co-expression of human reduced folate carrier half-molecules in transport-impaired K562 cells: localization of a substrate binding domain to transmembrane domains 7-12. J Biol Chem 2004 Nov 5 1
34 15705657 Adaptive regulation of intestinal thiamin uptake: molecular mechanism using wild-type and transgenic mice carrying hTHTR-1 and -2 promoters. Am J Physiol Gastrointest Liver Physiol 2005 Jun 2
35 15871139 Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3. Am J Hum Genet 2005 Jul 1
36 16055442 Differentiation-dependent up-regulation of intestinal thiamin uptake: cellular and molecular mechanisms. J Biol Chem 2005 Sep 23 2
37 16206251 Developmental maturation of intestinal and renal thiamin uptake: studies in wild-type and transgenic mice carrying human THTR-1 and 2 promoters. J Cell Physiol 2006 Feb 1
38 16373304 Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. Acta Paediatr 2006 Jan 1
39 16705148 Thiamin uptake by the human-derived renal epithelial (HEK-293) cells: cellular and molecular mechanisms. Am J Physiol Renal Physiol 2006 Oct 4
40 16790503 Biotin-responsive basal ganglia disease-linked mutations inhibit thiamine transport via hTHTR2: biotin is not a substrate for hTHTR2. Am J Physiol Cell Physiol 2006 Nov 3
41 16889681 Characteristics of thiamine uptake by the BeWo human trophoblast cell line. J Biochem Mol Biol 2006 Jul 31 3
42 17132746 Thiamine transporter mutation: an example of monogenic diabetes mellitus. Eur J Endocrinol 2006 Dec 2
43 17331069 Targeting and intracellular trafficking of clinically relevant hTHTR1 mutations in human cell lines. Clin Sci (Lond) 2007 Jul 3
44 17463047 Vitamin B1 (thiamine) uptake by human retinal pigment epithelial (ARPE-19) cells: mechanism and regulation. J Physiol 2007 Jul 1 4
45 17659067 Thiamine-responsive megaloblastic anaemia: a cause of syndromic diabetes in childhood. Pediatr Diabetes 2007 Aug 1
46 18614593 A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anemia syndrome. J Trop Pediatr 2009 Aug 2
47 19096015 Molecular genetics of alcohol-related brain damage. Alcohol Alcohol 2009 Mar-Apr 2
48 19347672 Thiamine responsive megaloblastic anemia syndrome. Indian J Pediatr 2009 Mar 4
49 19628653 Enteropathogenic Escherichia coli inhibits intestinal vitamin B1 (thiamin) uptake: studies with human-derived intestinal epithelial Caco-2 cells. Am J Physiol Gastrointest Liver Physiol 2009 Oct 2
50 19817279 Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness. Turk J Pediatr 2009 May-Jun 7