Caffeine markedly sensitizes human mesothelioma cell lines to pemetrexed

Por Min, Sang Hee, Goldman, I. David, Zhao, Rongbao
Publicado em 2007

A Role for the Proton-coupled Folate Transporter (PCFT-SLC46A1) in Folate Receptor-mediated Endocytosis

Por Zhao, Rongbao, Min, Sang Hee, Wang, Yanhua, Campanella, Estela, Low, Philip S., Goldman, I. David
Publicado em 2009

A renewed call for international representation in editorial boards of international psychiatry journals

Por Pike, Kathleen M., Min, Sang‐Hee, Poku, Ohemaa B., Reed, Geoffrey M., Saxena, Shekhar
Publicado no World Psychiatry (2017)

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

Por Shin, Daniel Sanghoon, Min, Sang Hee, Russell, Laura, Zhao, Rongbao, Fiser, Andras, Goldman, I. David
Publicado em 2010

The clinical course and genetic defect in the PCFT gene in a 27-year old woman with hereditary folate malabsorption

Por Min, Sang Hee, Oh, Sun Young, Karp, George I., Poncz, Mortimer, Zhao, Rongbao, Goldman, I. David
Publicado em 2008

Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption

Por Shin, Daniel Sanghoon, Mahadeo, Kris, Min, Sang Hee, Diop-Bove, Ndeye, Clayton, Peter, Zhao, Rongbao, Goldman, I. David
Publicado em 2011

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

Por Zhao, Rongbao, Min, Sang Hee, Qiu, Andong, Sakaris, Antoinette, Goldberg, Gary L., Sandoval, Claudio, Malatack, J. Jeffrey, Rosenblatt, David S., Goldman, I. David
Publicado em 2007

PIKfyve Deficiency in Myeloid Cells Impairs Lysosomal Homeostasis in Macrophages and Promotes Systemic Inflammation in Mice

Por Min, Sang Hee, Suzuki, Aae, Weaver, Lehn, Guzman, Jessica, Chung, Yutein, Jin, Huiyan, Gonzalez, Francina, Trasorras, Claire, Zhao, Liang, Spruce, Lynn A., Seeholzer, Steven H., Behrens, Edward M., Abrams, Charles S.
Publicado no Mol Cell Biol (2019)

Brief Report: Autistic Symptoms, Developmental Regression, Mental Retardation, Epilepsy, and Dyskinesias in CNS Folate Deficiency

Por Moretti, Paolo, Peters, Sarika U., del Gaudio, Daniela, Sahoo, Trilochan, Hyland, Keith, Bottiglieri, Teodoro, Hopkin, Robert J., Peach, Elizabeth, Min, Sang Hee, Goldman, David, Roa, Benjamin, Bacino, Carlos A., Scaglia, Fernando
Publicado em 2007