Novel riboflavin transporter family RFVT/SLC52: identification, nomenclature, functional characterization and genetic diseases of RFVT/SLC52
A Yonezawa, K Inui - Molecular aspects of medicine, 2013 - Elsevier
Riboflavin, a water-soluble vitamin also known as vitamin B2, is essential for normal cellular
functions. Riboflavin transporters play important roles in its homeostasis. Recently, three …
functions. Riboflavin transporters play important roles in its homeostasis. Recently, three …
Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1
A Yonezawa, S Masuda… - American Journal of …, 2008 - journals.physiology.org
Absorption of riboflavin is mediated by transporter (s). However, a mammalian riboflavin
transporter has yet to be identified. In the present study, the novel human and rat riboflavin …
transporter has yet to be identified. In the present study, the novel human and rat riboflavin …
[HTML][HTML] Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brain
Y Yao, A Yonezawa, H Yoshimatsu, S Masuda… - The Journal of …, 2010 - Elsevier
We isolated cDNA coding a new human riboflavin transporter (hRFT) 3, which exhibits 86.7
and 44.1% amino acid identity with hRFT1 and hRFT2, respectively. It was predicted to have …
and 44.1% amino acid identity with hRFT1 and hRFT2, respectively. It was predicted to have …
Identification and functional characterization of rat riboflavin transporter 2
S Yamamoto, K Inoue, K Ohta, R Fukatsu… - Journal of …, 2009 - academic.oup.com
We have newly identified rat riboflavin transporter 2 (rRFT2) and its human orthologue
(hRFT2), and carried out detailed functional characterization of rRFT2. The mRNA of rRFT2 …
(hRFT2), and carried out detailed functional characterization of rRFT2. The mRNA of rRFT2 …
An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency
B O'Callaghan, AM Bosch… - Journal of Inherited …, 2019 - Wiley Online Library
Riboflavin transporter deficiency (RTD) is a rare neurological condition that encompasses
the Brown‐Vialetto‐Van Laere and Fazio‐Londe syndromes since the discovery of …
the Brown‐Vialetto‐Van Laere and Fazio‐Londe syndromes since the discovery of …
[HTML][HTML] Functional characteristics of the human ortholog of riboflavin transporter 2 and riboflavin-responsive expression of its rat ortholog in the small intestine indicate …
M Fujimura, S Yamamoto, T Murata, T Yasujima… - The Journal of …, 2010 - Elsevier
Riboflavin transporter (RFT) 2 has recently been identified as a transporter that may be,
mainly based on the functional characteristics of its rat ortholog (rRFT2), involved in the …
mainly based on the functional characteristics of its rat ortholog (rRFT2), involved in the …
Clinical presentation and outcome of riboflavin transporter deficiency: mini review after five years of experience
B Jaeger, AM Bosch - Journal of inherited metabolic disease, 2016 - Springer
Introduction Riboflavin (vitamin B2) is absorbed in the small intestine by the human
riboflavin transporters RFVT1 and RFVT3. A third riboflavin transporter (RFVT2) is …
riboflavin transporters RFVT1 and RFVT3. A third riboflavin transporter (RFVT2) is …
Role of cysteine residues in cell surface expression of the human riboflavin transporter-2 (hRFT2) in intestinal epithelial cells
VS Subramanian, L Rapp… - American Journal of …, 2011 - journals.physiology.org
The water-soluble vitamin B2 (riboflavin, RF) is an essential micronutrient for normal cell
function and survival. Recent studies have identified a role for the human riboflavin …
function and survival. Recent studies have identified a role for the human riboflavin …
Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome
TB Haack, C Makowski, Y Yao, E Graf… - Journal of inherited …, 2012 - Springer
Abstract Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological
disorder characterized by infancy onset sensorineural deafness and ponto-bulbar palsy …
disorder characterized by infancy onset sensorineural deafness and ponto-bulbar palsy …
[HTML][HTML] Differential expression of human riboflavin transporters-1,-2, and-3 in polarized epithelia: a key role for hRFT-2 in intestinal riboflavin uptake
VS Subramanian, SB Subramanya, L Rapp… - … et Biophysica Acta (BBA …, 2011 - Elsevier
Transport of riboflavin (RF) across both the brush border membrane (BBM) and basolateral
membrane (BLM) of the polarized enterocyte occurs via specific carrier-mediated …
membrane (BLM) of the polarized enterocyte occurs via specific carrier-mediated …
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