نتایج جستجو برای: slc19a1

تعداد نتایج: 126  

2015
Shaik Mohammad Naushad Addepalli Pavani Raghunadha Rao Digumarti Suryanarayana Raju Gottumukkala Vijay Kumar Kutala

Received 26 January 2011 Revised 28 January 2011 Accepted 29 January 2011 Early online 29 January 2011 Print 31 January 2011 This study addresses the issues in translating the laboratory derived data obtained during discovery phase of research to a clinical setting using a breast cancer model. Laboratory-based risk assessment indicated that a family history of breast cancer, reduced folate carr...

Journal: :The Journal of biological chemistry 1998
R Zhao Y G Assaraf I D Goldman

In an ongoing study of structure-function relationships of the murine reduced folate carrier 1 (RFC1), a glutamate to lysine mutation at amino acid 45 was identified in a methotrexate (MTX)-resistant L1210 clonal variant in which MTX and 5-formyltetrahydrofolate (5-CHO-THF) influx was markedly decreased. The characteristics of the mutated carrier, RFC1-E45K, were studied by cDNA transfection in...

Journal: :Progress in neuro-psychopharmacology & biological psychiatry 2018
Tanusree Saha Mahasweta Chatterjee Deepak Verma Anirban Ray Swagata Sinha Usha Rajamma Kanchan Mukhopadhyay

An etiologically complex disorder, Attention Deficit Hyperactivity Disorder (ADHD), is often associated with various levels of cognitive deficit. Folate/vitamin B9 is crucial for numerous biochemical pathways including neural stem cell proliferation and differentiation, regulation of gene expression, neurotransmitter synthesis, myelin synthesis and repair, etc. and a scarcity has often been lin...

Journal: :Neuroscience letters 2014
Benjamin V Ineichen Salla Keskitalo Melinda Farkas Nadja Bain Ulf Kallweit Michael Weller Luisa Klotz Michael Linnebank

Methylenetetrahydrofolate reductase (MTHFR) is necessary for the synthesis of methionine and S-adenosylmethionine, which is necessary for CNS (re-)myelination. The MTHFR variant c.1298A>C was associated with the development of relapsing remitting multiple sclerosis (RRMS) in a German population. This study aimed at analyzing whether further genetic variants of methionine metabolism are associat...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011
Farhan J Bukhari Hamid Moradi Pavan Gollapudi Hyun Ju Kim Nosratola D Vaziri Hamid M Said

BACKGROUND Chronic kidney disease (CKD) is associated with significant cardiovascular, neurological and metabolic complications. Thiamin and folate are essential for growth, development and normal cellular function, and their uptake is mediated by regulated transport systems. While plasma folate and thiamin levels are generally normal in patients with CKD, they commonly exhibit features resembl...

Journal: :Cancer research 2005
David W L Ma Richard H Finnell Laurie A Davidson Evelyn S Callaway Ofer Spiegelstein Jorge A Piedrahita J Michael Salbaum Claudia Kappen Brad R Weeks Jill James Daniel Bozinov Joanne R Lupton Robert S Chapkin

Low dietary folate intake is associated with an increased risk for colon cancer; however, relevant genetic animal models are lacking. We therefore investigated the effect of targeted ablation of two folate transport genes, folate binding protein 1 (Folbp1) and reduced folate carrier 1 (RFC1), on folate homeostasis to elucidate the molecular mechanisms of folate action on colonocyte cell prolife...

2013
Sanja A. Farkas Anna K. Böttiger Helena S. Isaksson Richard H. Finnell Aiguo Ren Torbjörn K. Nilsson

The objectives of this study were to identify tissue-specific differentially methylated regions (T-DMR's) in the folate transport genes in placental tissue compared with leukocytes, and from placental tissues obtained from normal infants or with neural tube defects (NTDs). Using pyrosequencing, we developed methylation assays for the CpG islands (CGIs) and the CGI shore regions of the folate re...

Journal: :Molecular pharmacology 2000
R Zhao F Gao P J Wang I D Goldman

In previous reports, an E45K mutation in reduced folate carrier (RFC1) resulted in marked substrate-specific changes in folate binding and the induction of an obligatory inorganic anion requirement for carrier function. In this study, site-directed mutagenesis was employed to further characterize the role of glutamate-45 in carrier function by replacement with glutamine, arginine, aspartate, le...

Journal: :Indian journal of biochemistry & biophysics 2011
Shaik Mohammad Naushad Addepalli Pavani Yedluri Rupasree Deepti Sripurna Suryanarayana Raju Gottumukkala Raghunadha Rao Digumarti Vijay Kumar Kutala

The present study was aimed to investigate the modulatory role of plasma folate and eight putatively functional polymorphisms of one-carbon metabolism on catecholamine methyltransferase (COMT)-mediated oxidative DNA damage and breast cancer risk. Plasma folate and 8-oxo-2'-deoxyguanosine (8-oxodG) were estimated by commercially available kits, while polymorphisms were screened by PCR-RFLP and P...

Journal: :Nucleic acids research 2003
Chantal Guimond Nathalie Trudel Christian Brochu Nathalie Marquis Amal El Fadili Régis Peytavi Guylaine Briand Dave Richard Nadine Messier Barbara Papadopoulou Jacques Corbeil Michel G Bergeron Danielle Légaré Marc Ouellette

In the protozoan parasite Leishmania, drug resistance can be a complex phenomenon. Several metabolic pathways and membrane transporters are implicated in the resistance phenotype. To monitor the expression of these genes, we generated custom DNA microarrays with PCR fragments corresponding to 44 genes involved with drug resistance. Transcript profiling of arsenite and antimony resistant mutants...

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