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Adenocarcinoma
Interaction of 2,4-Diaminopyrimidine-Containing Drugs Including Fedratinib and Trimethoprim with Thiamine Transporters.
Anemia
Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype.
Anemia
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.
Anemia
Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent.
Anemia
Thiamine transporter mutation: an example of monogenic diabetes mellitus.
Anemia
Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings.
Anemia
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
Anemia
Thiamine-responsive megaloblastic anemia syndrome.
Anemia, Megaloblastic
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I.
Anemia, Megaloblastic
Cloning of the human thiamine transporter, a member of the folate transporter family.
Anemia, Megaloblastic
Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.
Anemia, Megaloblastic
Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype.
Anemia, Megaloblastic
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.
Anemia, Megaloblastic
Leber's Congenital Amaurosis as the Retinal Degenerative Phenotype in Thiamine Responsive Megaloblastic Anemia: A Case Report.
Anemia, Megaloblastic
Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.
Anemia, Megaloblastic
Mitochondria from cultured cells derived from normal and thiamine-responsive megaloblastic anemia individuals efficiently import thiamine diphosphate.
Anemia, Megaloblastic
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.
Anemia, Megaloblastic
Novel nonsense mutation (p.Ile411Metfs*12) in the SLC19A2 gene causing Thiamine Responsive Megaloblastic Anemia in an Indian patient.
Anemia, Megaloblastic
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
Anemia, Megaloblastic
The Effects of Genetic Mutations and Drugs on the Activity of the Thiamine Transporter, SLC19A2.
Anemia, Megaloblastic
Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent.
Anemia, Megaloblastic
Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings.
Anemia, Megaloblastic
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
Anemia, Megaloblastic
Thiamine-responsive megaloblastic anemia syndrome.
Anemia, Megaloblastic
Thiamine-responsive megaloblastic anemia syndrome: a novel mutation.
Anemia, Megaloblastic
Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness.
Anemia, Megaloblastic
[Hematologic manifestations of inborn errors of metabolism]
Basal Ganglia Diseases
Neuropathological characteristics of the brain in two patients with SLC19A3 mutations related to the biotin-thiamine-responsive basal ganglia disease.
Basal Ganglia Diseases
Stress-Induced Upregulation of SLC19A3 is Impaired in Biotin-Thiamine-Responsive Basal Ganglia Disease.
Beriberi
Analysis of thiamine transporter genes in sporadic beriberi.
Brain Diseases
Biotin-responsive basal ganglia disease: a case diagnosed by whole exome sequencing.
Brain Diseases
Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky Encephalopathy.
Brain Diseases
Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.
Breast Neoplasms
Down-regulation of thiamine transporter THTR2 gene expression in breast cancer and its association with resistance to apoptosis.
Breast Neoplasms
Hypoxia induced upregulation and function of the thiamine transporter, SLC19A3 in a breast cancer cell line.
Breast Neoplasms
Low-thiamine diet increases mammary tumor latency in FVB/N-Tg(MMTVneu) mice.
Breast Neoplasms
Sensitivity of breast cancer cell lines to recombinant thiaminase I.
Breast Neoplasms
Specific association of thiamine-coated gadolinium nanoparticles with human breast cancer cells expressing thiamine transporters.
Breast Neoplasms
Thiamine transporter gene expression and exogenous thiamine modulate the expression of genes involved in drug and prostaglandin metabolism in breast cancer cells.
Deafness
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I.
Deafness
Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.
Deafness
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
Deafness
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.
Deafness
Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent.
Deafness
Thiamine transporter mutation: an example of monogenic diabetes mellitus.
Deafness
Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings.
Deafness
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
Deafness
Thiamine-responsive megaloblastic anemia syndrome.
Diabetes Mellitus
Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians.
Diabetes Mellitus
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.
Diabetes Mellitus
Thiamine Prevents Obesity and Obesity-Associated Metabolic Disorders in OLETF Rats.
Diabetes Mellitus
Thiamine responsive megaloblastic anemia syndrome associated with patent ductus arteriosus: First case report from Kashmir Valley of the Indian subcontinent.
Diabetes Mellitus
Thiamine transporter mutation: an example of monogenic diabetes mellitus.
Diabetes Mellitus
Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: report of two siblings.
Diabetes Mellitus
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
Diabetes Mellitus
Thiamine-responsive megaloblastic anemia syndrome.
Diabetes Mellitus
Thiamine-responsive megaloblastic anemia syndrome: a novel mutation.
Diabetes Mellitus
Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness.
Diabetes Mellitus, Type 1
Thiamine transporter 2 is involved in high glucose-induced damage and altered thiamine availability in cell models of diabetic retinopathy.
Diabetes Mellitus, Type 2
Analysis of slc19a2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in pima indians.
Diabetes Mellitus, Type 2
Thiamine Prevents Obesity and Obesity-Associated Metabolic Disorders in OLETF Rats.
Diabetic Retinopathy
Thiamine transporter 2 is involved in high glucose-induced damage and altered thiamine availability in cell models of diabetic retinopathy.
Dystonia
Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.
Genetic Diseases, Inborn
The Effects of Genetic Mutations and Drugs on the Activity of the Thiamine Transporter, SLC19A2.
Hearing Loss, Sensorineural
Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype.
Hearing Loss, Sensorineural
Thiamine-responsive megaloblastic anemia syndrome: a novel mutation.
Homocystinuria
[Hematologic manifestations of inborn errors of metabolism]
Hyperglycemia
Reduced Thiamine Availability and Hyperglycemia Impair Thiamine Transport in Renal Glomerular Cells through Modulation of Thiamine Transporter 2.
Hypertension
Association of a SNP in SLC35F3 Gene with the Risk of Hypertension in a Chinese Han Population.
Hypertension
Genetic implication of a novel thiamine transporter in human hypertension.
Infections
Reduced Folate Carrier: an Entry Receptor for a Novel Feline Leukemia Virus Variant.
Infertility, Male
Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.
Korsakoff Syndrome
Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS).
Leigh Disease
Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata.
Leukemia
Dietary thiamine influences l-asparaginase sensitivity in a subset of leukemia cells.
Microcephaly
Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata.
Neoplasms
Down-regulation of thiamine transporter THTR2 gene expression in breast cancer and its association with resistance to apoptosis.
Neoplasms
Functional and mechanistic roles of the human proton-coupled folate transporter transmembrane domain 6-7 linker.
Neoplasms
Thiamine transporter gene expression and exogenous thiamine modulate the expression of genes involved in drug and prostaglandin metabolism in breast cancer cells.
Nervous System Diseases
Thiamine metabolism is critical for regulating correlated growth of dendrite arbors and neuronal somata.
Neurodegenerative Diseases
High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice.
Obesity
Low-thiamine diet increases mammary tumor latency in FVB/N-Tg(MMTVneu) mice.
Starvation
Sensitivity of breast cancer cell lines to recombinant thiaminase I.
Thiamine Deficiency
Drug-nutrient interactions: discovering prescription drug inhibitors of the thiamine transporter ThTR-2 (SLC19A3).
Thiamine Deficiency
HIF1-?-mediated gene expression induced by vitamin B1 deficiency.
Wernicke Encephalopathy
Stress-Induced Upregulation of SLC19A3 is Impaired in Biotin-Thiamine-Responsive Basal Ganglia Disease.
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THIQ_AGRFC
Agrobacterium fabrum (strain C58 / ATCC 33970)
238
0
25591
Swiss-Prot
-
THIQ_ALIF1
Aliivibrio fischeri (strain ATCC 700601 / ES114)
234
0
26174
Swiss-Prot
-
THIQ_BRUA2
Brucella abortus (strain 2308)
241
0
26187
Swiss-Prot
-
THIQ_BRUAB
Brucella abortus biovar 1 (strain 9-941)
241
0
26187
Swiss-Prot
-
THIQ_BRUME
Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094)
241
0
26171
Swiss-Prot
-
THIQ_RUEST
Ruegeria sp. (strain TM1040)
231
0
24701
Swiss-Prot
-
THIQ_SALCH
Salmonella choleraesuis (strain SC-B67)
235
0
25634
Swiss-Prot
-
THIQ_SALPA
Salmonella paratyphi A (strain ATCC 9150 / SARB42)
235
0
25604
Swiss-Prot
-
THIQ_SALTI
235
0
25574
Swiss-Prot
-
THIQ_SALTY
Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
235
0
25571
Swiss-Prot
-
THIQ_SHIBS
Shigella boydii serotype 4 (strain Sb227)
232
0
25016
Swiss-Prot
-
THIQ_SHIDS
Shigella dysenteriae serotype 1 (strain Sd197)
232
0
25045
Swiss-Prot
-
THIQ_SHIF8
Shigella flexneri serotype 5b (strain 8401)
232
0
25051
Swiss-Prot
-
THIQ_SHIFL
232
0
25097
Swiss-Prot
-
THIQ_SHISS
Shigella sonnei (strain Ss046)
232
0
25041
Swiss-Prot
-
THIQ_SODGM
Sodalis glossinidius (strain morsitans)
232
0
25290
Swiss-Prot
-
THIQ_VIBCH
Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961)
238
0
26238
Swiss-Prot
-
THIQ_VIBPA
Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633)
234
0
25969
Swiss-Prot
-
THIQ_VIBVU
Vibrio vulnificus (strain CMCP6)
234
0
25793
Swiss-Prot
-
THIQ_VIBVY
Vibrio vulnificus (strain YJ016)
234
0
25793
Swiss-Prot
-
THIQ_YERPA
Yersinia pestis bv. Antiqua (strain Antiqua)
236
0
25620
Swiss-Prot
-
THIQ_YERPE
236
0
25620
Swiss-Prot
-
THIQ_YERPN
Yersinia pestis bv. Antiqua (strain Nepal516)
236
0
25620
Swiss-Prot
-
THIQ_YERPS
Yersinia pseudotuberculosis serotype I (strain IP32953)
236
0
25627
Swiss-Prot
-
THIQ_BRUSU
Brucella suis biovar 1 (strain 1330)
241
0
26171
Swiss-Prot
-
THIQ_CERS4
Cereibacter sphaeroides (strain ATCC 17023 / DSM 158 / JCM 6121 / CCUG 31486 / LMG 2827 / NBRC 12203 / NCIMB 8253 / ATH 2.4.1.)
231
0
24241
Swiss-Prot
-
THIQ_CHESB
Chelativorans sp. (strain BNC1)
246
0
26647
Swiss-Prot
-
THIQ_ECO57
232
0
25025
Swiss-Prot
-
THIQ_ECOL5
Escherichia coli O6:K15:H31 (strain 536 / UPEC)
232
0
25102
Swiss-Prot
-
THIQ_ECOL6
Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC)
232
0
25093
Swiss-Prot
-
THIQ_ECOLI
Escherichia coli (strain K12)
232
0
24999
Swiss-Prot
-
THIQ_ECOUT
Escherichia coli (strain UTI89 / UPEC)
232
0
25088
Swiss-Prot
-
THIQ_HAEDU
Haemophilus ducreyi (strain 35000HP / ATCC 700724)
213
0
23915
Swiss-Prot
-
THIQ_HAEI8
Haemophilus influenzae (strain 86-028NP)
215
0
23740
Swiss-Prot
-
THIQ_HAEIN
Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd)
215
0
23727
Swiss-Prot
-
THIQ_HAES1
Haemophilus somnus (strain 129Pt)
214
0
24251
Swiss-Prot
-
THIQ_JANSC
Jannaschia sp. (strain CCS1)
229
0
24853
Swiss-Prot
-
THIQ_MANSM
Mannheimia succiniciproducens (strain MBEL55E)
215
0
24133
Swiss-Prot
-
THIQ_PASMU
Pasteurella multocida (strain Pm70)
225
0
25229
Swiss-Prot
-
THIQ_PECAS
Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672)
236
0
25943
Swiss-Prot
-
THIQ_PHOLL
Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01)
235
0
25926
Swiss-Prot
-
THIQ_PHOPR
Photobacterium profundum (strain SS9)
241
0
26634
Swiss-Prot
-
THIQ_RHILO
Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099)
253
0
26616
Swiss-Prot
-
THIQ_RHIME
Rhizobium meliloti (strain 1021)
238
0
25681
Swiss-Prot
-
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