Identification and characterization of the minimal 5′-regulatory region of the human riboflavin transporter-3 (SLC52A3) in intestinal epithelial cells
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Title
Identification and characterization of the minimal 5′-regulatory region of the human riboflavin transporter-3 (SLC52A3) in intestinal epithelial cells
Authors
Keywords
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Journal
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 308, Issue 2, Pages C189-C196
Publisher
American Physiological Society
Online
2014-11-14
DOI
10.1152/ajpcell.00342.2014
References
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Note: Only part of the references are listed.- Low activity of LSD1 elicits a pro-inflammatory gene expression profile in riboflavin-deficient human T Lymphoma Jurkat cells
- (2014) Dandan Liu et al. Genes and Nutrition
- Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases and a literature review in mainland Chinese patients
- (2014) Min Zhu et al. JOURNAL OF HUMAN GENETICS
- Differentiation-dependent regulation of intestinal vitamin B2 uptake: studies utilizing human-derived intestinal epithelial Caco-2 cells and native rat intestine
- (2013) Veedamali S. Subramanian et al. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
- Riboflavin deprivation inhibits macrophage viability and activity – a study on the RAW 264.7 cell line
- (2013) Agnieszka Irena Mazur-Bialy et al. BRITISH JOURNAL OF NUTRITION
- Riboflavin (vitamin B2) deficiency impairs NADPH oxidase 2 (Nox2) priming and defense againstListeria monocytogenes
- (2013) Michael Schramm et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Role of cysteine residues in cell surface expression of the human riboflavin transporter-2 (hRFT2) in intestinal epithelial cells
- (2011) Veedamali S. Subramanian et al. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
- Differential expression of human riboflavin transporters -1, -2, and -3 in polarized epithelia: A key role for hRFT-2 in intestinal riboflavin uptake
- (2011) Veedamali S. Subramanian et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
- Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment
- (2010) Annet M. Bosch et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Identification and Comparative Functional Characterization of a New Human Riboflavin Transporter hRFT3 Expressed in the Brain
- (2010) Yoshiaki Yao et al. JOURNAL OF NUTRITION
- Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies a susceptibility locus at PLCE1
- (2010) Li-Dong Wang et al. NATURE GENETICS
- Riboflavin Inhibits IL-6 Expression and p38 Activation in Islet Cells
- (2009) Lorenzo Cobianchi et al. CELL TRANSPLANTATION
- Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- (2009) Lap-Kay Law et al. CLINICA CHIMICA ACTA
- Identification and Functional Characterization of Rat Riboflavin Transporter 2
- (2009) S. Yamamoto et al. JOURNAL OF BIOCHEMISTRY
- ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- (2009) Wen-Chen Liang et al. NEUROMUSCULAR DISORDERS
- Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1
- (2008) Atsushi Yonezawa et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
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