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Sang Hee Min

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Publications

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Daniel Sanghoon Shin; Kris Michael Mahadeo; Sang Hee Min; Ndeye Diop-Bove; Peter Clayton; Rongbao Zhao; I David Goldman
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.
Daniel Sanghoon Shin; Sang Hee Min; Laura Russell; Rongbao Zhao; András Fiser; I David Goldman
Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.
Sang Hee Min; Sun Young Oh; George I Karp; Mortimer Poncz; Rongbao Zhao; I David Goldman
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption.

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All Publications

2011: Daniel Sanghoon Shin; Kris Michael Mahadeo; Sang Hee Min; Ndeye Diop-Bove; Peter Clayton; Rongbao Zhao; I David Goldman
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.
Molecular genetics and metabolism 2011;103(1):33-7.
2010: Daniel Sanghoon Shin; Sang Hee Min; Laura Russell; Rongbao Zhao; András Fiser; I David Goldman
Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.
Blood 2010;116(24):5162-9.
2008: Sang Hee Min; Sun Young Oh; George I Karp; Mortimer Poncz; Rongbao Zhao; I David Goldman
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption.
The Journal of pediatrics 2008;153(3):435-7.
2008: Sang Hee Min; I David Goldman; Rongbao Zhao
Caffeine markedly sensitizes human mesothelioma cell lines to pemetrexed.
Cancer chemotherapy and pharmacology 2008;61(5):819-27.
2007: Andong Qiu; Sang Hee Min; Michaela Jansen; Usha Malhotra; Eugenia Tsai; Diane C Cabelof; Larry H Matherly; Rongbao Zhao; Myles H Akabas; I David Goldman
Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction.
American journal of physiology. Cell physiology 2007;293(5):C1669-78.
2007: Rongbao Zhao; Sang Hee Min; Andong Qiu; Antoinette Sakaris; Gary L Goldberg; Claudio Sandoval; J Jeffrey Malatack; David S Rosenblatt; I David Goldman
The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.
Blood 2007;110(4):1147-52.
2007: Shrikanta Chattopadhyay; Roni Tamari; Sang Hee Min; Rongbao Zhao; Eugenia Tsai; I David Goldman
Commentary: a case for minimizing folate supplementation in clinical regimens with pemetrexed based on the marked sensitivity of the drug to folate availability.
The oncologist 2007;12(7):808-15.
2006: Andong Qiu; Michaela Jansen; Antoinette Sakaris; Sang Hee Min; Shrikanta Chattopadhyay; Eugenia Tsai; Claudio Sandoval; Rongbao Zhao; Myles H Akabas; I David Goldman
Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption.
Cell 2006;127(5):917-28.