Sang Hee Min[Author] - Search Results

Year	Number of Results
2006	1
2007	4
2008	4
2009	1
2010	1
2011	1
2017	1
2019	1
2024	0

1

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

Min SH, Suzuki A, Weaver L, Guzman J, Chung Y, Jin H, Gonzalez F, Trasorras C, Zhao L, Spruce LA, Seeholzer SH, Behrens EM, Abrams CS. Min SH, et al. Mol Cell Biol. 2019 Oct 11;39(21):e00158-19. doi: 10.1128/MCB.00158-19. Print 2019 Nov 1. Mol Cell Biol. 2019. PMID: 31427458 Free PMC article.

2

A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.

Zhao R, Min SH, Wang Y, Campanella E, Low PS, Goldman ID. Zhao R, et al. Among authors: min sh. J Biol Chem. 2009 Feb 13;284(7):4267-74. doi: 10.1074/jbc.M807665200. Epub 2008 Dec 11. J Biol Chem. 2009. PMID: 19074442 Free PMC article.

3

Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption.

Qiu A, Jansen M, Sakaris A, Min SH, Chattopadhyay S, Tsai E, Sandoval C, Zhao R, Akabas MH, Goldman ID. Qiu A, et al. Among authors: min sh. Cell. 2006 Dec 1;127(5):917-28. doi: 10.1016/j.cell.2006.09.041. Cell. 2006. PMID: 17129779 Free article.

4

Caffeine markedly sensitizes human mesothelioma cell lines to pemetrexed.

Min SH, Goldman ID, Zhao R. Min SH, et al. Cancer Chemother Pharmacol. 2008 Apr;61(5):819-27. doi: 10.1007/s00280-007-0539-z. Epub 2007 Jun 27. Cancer Chemother Pharmacol. 2008. PMID: 17594092 Free PMC article.

5

Brief report: autistic symptoms, developmental regression, mental retardation, epilepsy, and dyskinesias in CNS folate deficiency.

Moretti P, Peters SU, Del Gaudio D, Sahoo T, Hyland K, Bottiglieri T, Hopkin RJ, Peach E, Min SH, Goldman D, Roa B, Bacino CA, Scaglia F. Moretti P, et al. Among authors: min sh. J Autism Dev Disord. 2008 Jul;38(6):1170-7. doi: 10.1007/s10803-007-0492-z. Epub 2007 Nov 20. J Autism Dev Disord. 2008. PMID: 18027081 Free PMC article.

6

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

Pike KM, Min SH, Poku OB, Reed GM, Saxena S. Pike KM, et al. Among authors: min sh. World Psychiatry. 2017 Feb;16(1):106-107. doi: 10.1002/wps.20389. World Psychiatry. 2017. PMID: 28127918 Free PMC article. No abstract available.

7

Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction.

Qiu A, Min SH, Jansen M, Malhotra U, Tsai E, Cabelof DC, Matherly LH, Zhao R, Akabas MH, Goldman ID. Qiu A, et al. Among authors: min sh. Am J Physiol Cell Physiol. 2007 Nov;293(5):C1669-78. doi: 10.1152/ajpcell.00202.2007. Epub 2007 Sep 26. Am J Physiol Cell Physiol. 2007. PMID: 17898134 Free article.

8

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

Zhao R, Min SH, Qiu A, Sakaris A, Goldberg GL, Sandoval C, Malatack JJ, Rosenblatt DS, Goldman ID. Zhao R, et al. Among authors: min sh. Blood. 2007 Aug 15;110(4):1147-52. doi: 10.1182/blood-2007-02-077099. Epub 2007 Apr 19. Blood. 2007. PMID: 17446347 Free PMC article.

9

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

Shin DS, Min SH, Russell L, Zhao R, Fiser A, Goldman ID. Shin DS, et al. Among authors: min sh. Blood. 2010 Dec 9;116(24):5162-9. doi: 10.1182/blood-2010-06-291237. Epub 2010 Aug 30. Blood. 2010. PMID: 20805364 Free PMC article.

10

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

Min SH, Oh SY, Karp GI, Poncz M, Zhao R, Goldman ID. Min SH, et al. J Pediatr. 2008 Sep;153(3):435-7. doi: 10.1016/j.jpeds.2008.04.009. J Pediatr. 2008. PMID: 18718264 Free PMC article.

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