Showing 120 of 120on this page. Filters & sort apply to loaded results; URL updates for sharing.120 of 120 on this page
Cellular uptake of thiamine. THTR1 carrier (encoded by SLC19A2 gene ...
SLC19A2 Gene Thiamine-Responsive Megaloblastic Anemia Syndrome NGS ...
SLC19A2 Gene - GeneCards | S19A2 Protein | S19A2 Antibody
Schematic representation of the SLC19A2 gene with mutations identified ...
Sequence analysis of the SLC19A2 gene using by next generation ...
(PDF) Novel Mutation in the SLC19A2 Gene in an Iranian Family with ...
Symptoms and Testing information for SLC19A2 Gene Thiamine-Responsive
SLC19A2 Gene Thiamine-responsive megaloblastic anemia syndrome NGS ...
SLC19A2 Gene Test ZAR 6,700 | Early Detection for Rare Blood Disorder ...
Whole exome sequencing identifies a new mutation in the SLC19A2 gene ...
Intestinal uptake of thiamine. THTR1 carrier (encoded by SLC19A2 gene ...
(PDF) A novel mutation in the SLC19A2 gene in a Turkish male with ...
A novel mutation in the thiamine responsive megaloblastic anaemia gene ...
SLC19A2 expression in human and mouse islets. Representative ...
SLC19A2 expression is a determinant of growth at physiologically ...
Novel mutations were identified in the SLC19A2 gene. Sequences showed ...
Bone marrow fi ndings of Slc19a2 À / À and Slc19a2 þ / þ mice on a ...
Primers for the real-time PCR analyses of the expression of SLC19A2 and ...
Targeted disruption of Slc19a2 . ( A ) Maps of the Slc19a2 allele ...
Schematic representation of the predicted topology of the SLC19A2 ...
Figure 1 from Targeted disruption of Slc19a2, the gene encoding the ...
SLC19A2 Antibody (NBP3-12981): Novus Biologicals
a. SLC19A2 and SLC19A3 mRNA. Key: HK-2 cells (hollow bars) and human ...
ABR thresholds in Slc19a2 À / À and Slc19a2 þ / þ mice. ( A ) Responses ...
SLC19A2 Polyclonal Antibody | Invitrogen (PA5-78332)
SLC19A2 mutation in a family with autosomal dominant diabetes. A ...
Thiamin uptake by Slc19a2 À/À (diamonds), Slc19a2 þ/À (triangles) and ...
SLC19A2 promoted the mitochondrial respiration of NONO-TFE3 rRCC by ...
(PDF) Targeted disruption of SLC19A2, the gene encoding the high ...
The role of pancreatic Slc19a2 expression in diabetes and thiamine ...
(PDF) Identification of a SLC19A2 nonsense mutation in Persian families ...
Common mechanisms of drug-induced megaloblastic anemia and SLC19A2 ...
pH-dependent pyridoxine transport by SLC19A2 and SLC19A3: Implications ...
Full-length SLC19A2 (A) and SLC19A3 (B) promoters in pGL3-Basic were ...
Retention of mutant SLC19A2 protein in cytoplasm is associated with ...
SLC19A2 Antibody (NBP2-88285): Novus Biologicals
a mRNA of SLC19A2 and SLC19A3 genes, relative to β-actin (n = 8). b ...
Table 1 from Identification of four SLC19A2 mutations in four Chinese ...
Subcellular - SLC19A2 - The Human Protein Atlas
A: role of specificity protein-1 (Sp1) sites in SLC19A2 and SLC19A3 ...
Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes ...
SLC9A2 Gene - GeneCards | SL9A2 Protein | SL9A2 Antibody
(PDF) A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family ...
Association between SLC19A2 rs2038024 polymorphism and patients ...
SLC19A2 Mutation analysis: Chromatograms showing the location of the ...
Invitrogen SLC19A2 Polyclonal Antibody 100 μL; Unconjugated:Antibodies ...
SLC19A2 Antibody, Novus Biologicals 100 μL; Unconjugated:Antibodies ...
Schematic representation of homozygous novel exon 2 deletion mutation ...
Inherited disorders of vitamin metabolism - European Journal of ...
Role of HIF-1α in the Hypoxia Inducible Expression of the Thiamine ...
Thiamine-responsive megaloblastic anemia | Semantic Scholar
Thiamine-Responsive Megaloblastic Anemia: Identification of Novel ...
(PDF) A novel mutation in the thiamine responsive megaloblastic anaemia ...
Differentiation-dependent Up-regulation of Intestinal Thiamin Uptake ...
SLC19A2抗体 (GTX131042) | GeneTex中国官方网站
In vitro and in vivo characterization of the minimal promoter region of ...
Identification of the Receptor Used by the Ecotropic Mouse GLN ...
Mutational topology of the SLC19A transporter proteins. A, truncation ...
Addgene: pDONR221_SLC19A2
RCSB PDB - 8Z80: SLC19A2-Pyridoxine inward structure
Several genetic defects cause alterations in the thiamine transporters ...
RCSB PDB - 8Z7Z: SLC19A2-Thiamine inward structure
Substrate transport and drug interaction of human thiamine transporters ...
Analyses of the substrate discrimination mechanism of SLC19 subfamily ...
双硫死亡 | 发现的细胞 “新” 型死亡方式-MedChemExpress - 脉脉
(PDF) Thiamine-responsive megaloblastic anemia (TRMA) in an Austrian ...
The Effects of Genetic Mutations and Drugs on the Activity of the ...
Relative contribution of THTR-1 and THTR-2 in thiamin uptake by ...
Differential Glucocorticoid Receptor-mediated Transcription Mechanisms ...
Figure 2 from Recurrent Stroke in a Child with TRMA Syndrome and ...
Pyridoxine uptake in HEK293 cells transiently expressing SLC19A ...
Figure 1 from Recurrent Stroke in a Child with TRMA Syndrome and ...
Figure 3 from Recurrent Stroke in a Child with TRMA Syndrome and ...
Frontiers | Elevated thiamine level is associated with activating ...
Heterozygosity in his father is shown for the detected variant in ...
Nature | 揭示SLC19A1对环二核苷酸和叶酸识别的分子机理 - 知乎
Amino Acid Transport by Epithelial Membranes - PMC
(PDF) Deletion of SLC19A2, the High Affinity Thiamine Transporter ...
Dietary thiamine intake influences ASNase sensitivity of SLC19A2-low ...
