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Journal Articles

Pcft Is Silenced By DNA Methylation In Pediatric Acute Lymphoblastic Leukemia Resulting In Decreased Methotrexate Uptake

Calvin K. Lee, MD, Weijie Poh, Megan Healey, PhD, Eric S Schafer, MD, Patrick Brown, MD, James G. Herman, MD

Blood (2013) 122 (21): 3768.

https://doi.org/10.1182/blood.V122.21.3768.3768

Published: 2013

Journal Articles

Knocking out the PCFT

Donald W. Jacobsen

Blood (2011) 117 (18): 4683–4685.

https://doi.org/10.1182/blood-2011-03-340398

Published: 2011

Journal Articles

A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency

Konstantin V. Salojin, Robert M. Cabrera, Weimei Sun, Wei Chun Chang, Colin Lin, Lindsay Duncan, Ken A. Platt, Robert Read, Peter Vogel, Qingyun Liu, Richard H. Finnell, Tamas Oravecz

Blood (2011) 117 (18): 4895–4904.

https://doi.org/10.1182/blood-2010-04-279653

Published: 2011

Journal Articles

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

Daniel Sanghoon Shin, Sang Hee Min, Laura Russell, Rongbao Zhao, Andras Fiser, I. David Goldman

Blood (2010) 116 (24): 5162–5169.

https://doi.org/10.1182/blood-2010-06-291237

Published: 2010

Journal Articles

A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

Inbal Lasry, Bluma Berman, Rachel Straussberg, Yael Sofer, Hanna Bessler, Mohamad Sharkia, Fabian Glaser, Gerrit Jansen, Stavit Drori, Yehuda G. Assaraf

Blood (2008) 112 (5): 2055–2061.

https://doi.org/10.1182/blood-2008-04-150276

Published: 2008

Includes: Supplemental data

Journal Articles

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

Rongbao Zhao, Sang Hee Min, Andong Qiu, Antoinette Sakaris, Gary L. Goldberg, Claudio Sandoval, J. Jeffrey Malatack, David S. Rosenblatt, I. David Goldman

Blood (2007) 110 (4): 1147–1152.

https://doi.org/10.1182/blood-2007-02-077099

Published: 2007

NARROW

Pcft Is Silenced By DNA Methylation In Pediatric Acute Lymphoblastic Leukemia Resulting In Decreased Methotrexate Uptake

Knocking out the PCFT

A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

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ASH Publications

American Society of Hematology

Pcft Is Silenced By DNA Methylation In Pediatric Acute Lymphoblastic Leukemia Resulting In Decreased Methotrexate Uptake

Knocking out the PCFT

A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

Email alerts

ASH Publications

American Society of Hematology

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