Sang Hee Min - Concepedia

Concepedia

Author

Sang Hee Min

Albert Einstein College of Medicine

Also Known As

Sang H Min, Sang H. Min, Sang Hee Min, Sang Min, Sang H. Min, 서울대학교 보건대학원

44

Publications

1.8K

Citations

16

H-Index

55

Concepts

All Affiliations

Albert Einstein College of Medicine University of Pennsylvania Children's Hospital of Philadelphia University of Michigan University College London

SH

About

Sang Hee Min is an author at Albert Einstein College of Medicine specializing in medicine, pathology, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.2K
2	Education	1	1	88
3	Health Sciences	1	1	88
4	Natural Sciences	1	1	46
5	Public Health	1	1	127

Sang Hee Min

×

16

Publications

1.8K

Citations

15

H-Index

	Year	Citations
Identification of an Intestinal Folate Transporter and the Molecular Basis for Hereditary Folate Malabsorption Andong Qiu, Michaela Jansen, Antoinette Sakaris, Cell BiochemistryGeneticsGastroenterologyPathologyIntestinal Folate Transporter	2006	830
A Role for the Proton-coupled Folate Transporter (PCFT-SLC46A1) in Folate Receptor-mediated Endocytosis Rongbao Zhao, Sang Hee Min, Yanhua Wang, Journal of Biological Chemistry	2008	156
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, Blood	2007	152
Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction Andong Qiu, Sang Hee Min, Michaela Jansen, American Journal of Physiology-Cell Physiology NutritionFunctional PropertiesSecondary StructureDigestive TractRodent Pcfts	2007	127
Brief Report: Autistic Symptoms, Developmental Regression, Mental Retardation, Epilepsy, and Dyskinesias in CNS Folate Deficiency Paolo Moretti, Sarika U. Peters, Daniela del Gaudio, Journal of Autism and Developmental Disorders Neurodevelopmental DisordersPsychiatryBrain DevelopmentDevelopmental DisordersDevelopmental Regression	2007	88
The Clinical Course and Genetic Defect in the PCFT Gene in a 27-Year-Old Woman with Hereditary Folate Malabsorption Sang Hee Min, Sun Young Oh, George Karp, The Journal of Pediatrics Clinical CourseMendelian DisorderPcft GeneGenetic DisorderGenetics	2008	61
Loss of PIKfyve in platelets causes a lysosomal disease leading to inflammation and thrombosis in mice Sang Hee Min, Aae Suzuki, Timothy J. Stalker, Nature Communications ImmunologyBlood CellPathologyCell DeathInflammation	2014	53
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, Blood	2010	53
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption Daniel Sanghoon Shin, Kris M. Mahadeo, Sang Hee Min, Molecular Genetics and Metabolism Mendelian DisorderBiochemistryNatural SciencesInherited Metabolic DiseaseNovel Mutations	2011	46
RhoA Is Essential for Maintaining Normal Megakaryocyte Ploidy and Platelet Generation Aae Suzuki, Jae‐Won Shin, Yuhuan Wang, PLoS ONE Platelet GenerationNormal Megakaryocyte PloidyBlood CellPlatelet PathobiologyCell Culture	2013	40

Page 1