7.6.2.15 Adenocarcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27803021&form=6&db=m Interaction of 2,4-Diaminopyrimidine-Containing Drugs Including Fedratinib and Trimethoprim with Thiamine Transporters. diagnostic usage,ongoing research,therapeutic application,unassigned 3,4,4,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10391222&form=6&db=m The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. ongoing research,unassigned 1,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16373304&form=6&db=m Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. causal interaction,unassigned 2,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16642288&form=6&db=m Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype. diagnostic usage,unassigned 1,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17132746&form=6&db=m Thiamine transporter mutation: an example of monogenic diabetes mellitus. causal interaction,unassigned 3,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18556972&form=6&db=m Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings. causal interaction,unassigned 4,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20835854&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome. causal interaction,unassigned 3,0 7.6.2.15 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22837935&form=6&db=m Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent. causal interaction,unassigned 1,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10074490&form=6&db=m Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts. unassigned - 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10391223&form=6&db=m Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. unassigned - 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10542220&form=6&db=m Cloning of the human thiamine transporter, a member of the folate transporter family. unassigned - 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10978358&form=6&db=m A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I. causal interaction,unassigned 4,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12014993&form=6&db=m Mitochondria from cultured cells derived from normal and thiamine-responsive megaloblastic anemia individuals efficiently import thiamine diphosphate. ongoing research,unassigned 4,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12205794&form=6&db=m [Hematologic manifestations of inborn errors of metabolism] diagnostic usage,unassigned 1,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14567973&form=6&db=m Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2. causal interaction,ongoing research,unassigned 3,2,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16373304&form=6&db=m Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. causal interaction,unassigned 2,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16642288&form=6&db=m Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype. diagnostic usage,unassigned 1,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18556972&form=6&db=m Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings. causal interaction,unassigned 4,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19817279&form=6&db=m Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness. unassigned - 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20835854&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome. causal interaction,unassigned 3,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22369132&form=6&db=m Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. causal interaction,unassigned 4,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22837935&form=6&db=m Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent. causal interaction,unassigned 1,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22876572&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome: a novel mutation. causal interaction,unassigned 2,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23638917&form=6&db=m Leber's Congenital Amaurosis as the Retinal Degenerative Phenotype in Thiamine Responsive Megaloblastic Anemia: A Case Report. causal interaction,unassigned 3,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26549656&form=6&db=m Novel nonsense mutation (p.Ile411Metfs*12) in the SLC19A2 gene causing Thiamine Responsive Megaloblastic Anemia in an Indian patient. causal interaction,unassigned 3,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28004468&form=6&db=m First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G. causal interaction,unassigned 1,0 7.6.2.15 Anemia, Megaloblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33649974&form=6&db=m The Effects of Genetic Mutations and Drugs on the Activity of the Thiamine Transporter, SLC19A2. causal interaction,unassigned 2,0 7.6.2.15 Basal Ganglia Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24372704&form=6&db=m Stress-Induced Upregulation of SLC19A3 is Impaired in Biotin-Thiamine-Responsive Basal Ganglia Disease. causal interaction,therapeutic application,unassigned 2,1,0 7.6.2.15 Basal Ganglia Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28677371&form=6&db=m Neuropathological characteristics of the brain in two patients with SLC19A3 mutations related to the biotin-thiamine-responsive basal ganglia disease. causal interaction,unassigned 3,0 7.6.2.15 Beriberi http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24607307&form=6&db=m Analysis of thiamine transporter genes in sporadic beriberi. unassigned - 7.6.2.15 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22777947&form=6&db=m Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency. causal interaction,unassigned 4,0 7.6.2.15 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23469184&form=6&db=m Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky Encephalopathy. causal interaction,unassigned 2,0 7.6.2.15 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25876998&form=6&db=m Biotin-responsive basal ganglia disease: a case diagnosed by whole exome sequencing. unassigned - 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12643751&form=6&db=m Specific association of thiamine-coated gadolinium nanoparticles with human breast cancer cells expressing thiamine transporters. ongoing research,unassigned 3,0 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12861052&form=6&db=m Down-regulation of thiamine transporter THTR2 gene expression in breast cancer and its association with resistance to apoptosis. causal interaction,ongoing research,therapeutic application,unassigned 4,2,1,0 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15328374&form=6&db=m Thiamine transporter gene expression and exogenous thiamine modulate the expression of genes involved in drug and prostaglandin metabolism in breast cancer cells. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,3,0 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19830429&form=6&db=m Sensitivity of breast cancer cell lines to recombinant thiaminase I. causal interaction,ongoing research,therapeutic application,unassigned 4,4,4,0 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20930543&form=6&db=m Hypoxia induced upregulation and function of the thiamine transporter, SLC19A3 in a breast cancer cell line. causal interaction,ongoing research,unassigned 1,2,0 7.6.2.15 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23591667&form=6&db=m Low-thiamine diet increases mammary tumor latency in FVB/N-Tg(MMTVneu) mice. causal interaction,ongoing research,unassigned 1,4,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10391222&form=6&db=m The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. ongoing research,unassigned 1,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10978358&form=6&db=m A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I. causal interaction,unassigned 4,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14567973&form=6&db=m Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2. causal interaction,ongoing research,unassigned 3,2,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16373304&form=6&db=m Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. causal interaction,unassigned 2,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17132746&form=6&db=m Thiamine transporter mutation: an example of monogenic diabetes mellitus. causal interaction,unassigned 3,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18556972&form=6&db=m Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings. causal interaction,unassigned 4,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20835854&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome. causal interaction,unassigned 3,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22369132&form=6&db=m Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. causal interaction,unassigned 4,0 7.6.2.15 Deafness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22837935&form=6&db=m Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent. causal interaction,unassigned 1,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11286512&form=6&db=m Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians. ongoing research,therapeutic application,unassigned 1,1,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16373304&form=6&db=m Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. causal interaction,unassigned 2,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17132746&form=6&db=m Thiamine transporter mutation: an example of monogenic diabetes mellitus. causal interaction,unassigned 3,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18556972&form=6&db=m Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings. causal interaction,unassigned 4,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19817279&form=6&db=m Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness. unassigned - 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20835854&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome. causal interaction,unassigned 3,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21422702&form=6&db=m Thiamine Prevents Obesity and Obesity-Associated Metabolic Disorders in OLETF Rats. causal interaction,unassigned 3,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22837935&form=6&db=m Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent. causal interaction,unassigned 1,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22876572&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome: a novel mutation. causal interaction,unassigned 2,0 7.6.2.15 Diabetes Mellitus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28004468&form=6&db=m First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G. causal interaction,unassigned 1,0 7.6.2.15 Diabetes Mellitus, Type 1 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31726874&form=6&db=m Thiamine transporter 2 is involved in high glucose-induced damage and altered thiamine availability in cell models of diabetic retinopathy. causal interaction,ongoing research,therapeutic application,unassigned 2,2,2,0 7.6.2.15 Diabetes Mellitus, Type 2 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11286512&form=6&db=m Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians. ongoing research,therapeutic application,unassigned 1,1,0 7.6.2.15 Diabetes Mellitus, Type 2 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21422702&form=6&db=m Thiamine Prevents Obesity and Obesity-Associated Metabolic Disorders in OLETF Rats. causal interaction,unassigned 3,0 7.6.2.15 Diabetic Retinopathy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31726874&form=6&db=m Thiamine transporter 2 is involved in high glucose-induced damage and altered thiamine availability in cell models of diabetic retinopathy. causal interaction,ongoing research,therapeutic application,unassigned 2,2,2,0 7.6.2.15 Dystonia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22777947&form=6&db=m Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency. causal interaction,unassigned 4,0 7.6.2.15 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33649974&form=6&db=m The Effects of Genetic Mutations and Drugs on the Activity of the Thiamine Transporter, SLC19A2. causal interaction,unassigned 2,0 7.6.2.15 Hearing Loss, Sensorineural http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16642288&form=6&db=m Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype. diagnostic usage,unassigned 1,0 7.6.2.15 Hearing Loss, Sensorineural http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22876572&form=6&db=m Thiamine-responsive megaloblastic anemia syndrome: a novel mutation. causal interaction,unassigned 2,0 7.6.2.15 Homocystinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12205794&form=6&db=m [Hematologic manifestations of inborn errors of metabolism] diagnostic usage,unassigned 1,0 7.6.2.15 Hyperglycemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33916491&form=6&db=m Reduced Thiamine Availability and Hyperglycemia Impair Thiamine Transport in Renal Glomerular Cells through Modulation of Thiamine Transporter 2. therapeutic application,unassigned 1,0 7.6.2.15 Hypertension http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24509276&form=6&db=m Genetic implication of a novel thiamine transporter in human hypertension. causal interaction,ongoing research,unassigned 3,2,0 7.6.2.15 Hypertension http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27379158&form=6&db=m Association of a SNP in SLC35F3 Gene with the Risk of Hypertension in a Chinese Han Population. causal interaction,therapeutic application,unassigned 3,2,0 7.6.2.15 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30996094&form=6&db=m Reduced Folate Carrier: an Entry Receptor for a Novel Feline Leukemia Virus Variant. causal interaction,therapeutic application,unassigned 3,1,0 7.6.2.15 Infertility, Male http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14567973&form=6&db=m Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2. causal interaction,ongoing research,unassigned 3,2,0 7.6.2.15 Korsakoff Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16015585&form=6&db=m Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS). unassigned - 7.6.2.15 Leigh Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28706281&form=6&db=m Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata. causal interaction,therapeutic application,unassigned 2,1,0 7.6.2.15 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33036978&form=6&db=m Dietary thiamine influences l-asparaginase sensitivity in a subset of leukemia cells. causal interaction,ongoing research,therapeutic application,unassigned 4,3,4,0 7.6.2.15 Microcephaly http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28706281&form=6&db=m Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata. causal interaction,therapeutic application,unassigned 2,1,0 7.6.2.15 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12861052&form=6&db=m Down-regulation of thiamine transporter THTR2 gene expression in breast cancer and its association with resistance to apoptosis. causal interaction,ongoing research,therapeutic application,unassigned 4,2,1,0 7.6.2.15 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15328374&form=6&db=m Thiamine transporter gene expression and exogenous thiamine modulate the expression of genes involved in drug and prostaglandin metabolism in breast cancer cells. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,3,0 7.6.2.15 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27514717&form=6&db=m Functional and mechanistic roles of the human proton-coupled folate transporter transmembrane domain 6-7 linker. causal interaction,unassigned 1,0 7.6.2.15 Nervous System Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28706281&form=6&db=m Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata. causal interaction,therapeutic application,unassigned 2,1,0 7.6.2.15 Neurodegenerative Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28665968&form=6&db=m High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice. causal interaction,unassigned 3,0 7.6.2.15 Obesity http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23591667&form=6&db=m Low-thiamine diet increases mammary tumor latency in FVB/N-Tg(MMTVneu) mice. causal interaction,ongoing research,unassigned 1,4,0 7.6.2.15 Starvation http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19830429&form=6&db=m Sensitivity of breast cancer cell lines to recombinant thiaminase I. causal interaction,ongoing research,therapeutic application,unassigned 4,4,4,0 7.6.2.15 Thiamine Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24846908&form=6&db=m HIF1-?-mediated gene expression induced by vitamin B1 deficiency. causal interaction,ongoing research,unassigned 3,3,0 7.6.2.15 Thiamine Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31764942&form=6&db=m Drug-nutrient interactions: discovering prescription drug inhibitors of the thiamine transporter ThTR-2 (SLC19A3). ongoing research,therapeutic application,unassigned 2,4,0 7.6.2.15 Wernicke Encephalopathy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24372704&form=6&db=m Stress-Induced Upregulation of SLC19A3 is Impaired in Biotin-Thiamine-Responsive Basal Ganglia Disease. causal interaction,therapeutic application,unassigned 2,1,0