Goldman ID - Search Results

1

Structural basis of antifolate recognition and transport by PCFT.

Parker JL, Deme JC, Kuteyi G, Wu Z, Huo J, Goldman ID, Owens RJ, Biggin PC, Lea SM, Newstead S. Parker JL, et al. Among authors: goldman id. Nature. 2021 Jul;595(7865):130-134. doi: 10.1038/s41586-021-03579-z. Epub 2021 May 26. Nature. 2021. PMID: 34040256 Free PMC article.

2

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: goldman id. 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.

3

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: goldman id. 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.

4

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: goldman id. 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.

5

Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function.

Najmi M, Zhao R, Fiser A, Goldman ID. Najmi M, et al. Among authors: goldman id. Am J Physiol Cell Physiol. 2016 Jul 1;311(1):C150-7. doi: 10.1152/ajpcell.00084.2016. Epub 2016 Jun 1. Am J Physiol Cell Physiol. 2016. PMID: 27251438 Free PMC article.

6

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. Among authors: goldman id. J Pediatr. 2008 Sep;153(3):435-7. doi: 10.1016/j.jpeds.2008.04.009. J Pediatr. 2008. PMID: 18718264 Free PMC article.

7

A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.

Diop-Bove N, Jain M, Scaglia F, Goldman ID. Diop-Bove N, et al. Among authors: goldman id. Gene. 2013 Sep 25;527(2):673-4. doi: 10.1016/j.gene.2013.06.039. Epub 2013 Jun 28. Gene. 2013. PMID: 23816405 Free PMC article.

8

Hypermethylation of the human proton-coupled folate transporter (SLC46A1) minimal transcriptional regulatory region in an antifolate-resistant HeLa cell line.

Diop-Bove NK, Wu J, Zhao R, Locker J, Goldman ID. Diop-Bove NK, et al. Among authors: goldman id. Mol Cancer Ther. 2009 Aug;8(8):2424-31. doi: 10.1158/1535-7163.MCT-08-0938. Epub 2009 Aug 11. Mol Cancer Ther. 2009. PMID: 19671745 Free PMC article.

9

Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption.

Mahadeo K, Diop-Bove N, Shin D, Unal ES, Teo J, Zhao R, Chang MH, Fulterer A, Romero MF, Goldman ID. Mahadeo K, et al. Among authors: goldman id. Am J Physiol Cell Physiol. 2010 Nov;299(5):C1153-61. doi: 10.1152/ajpcell.00113.2010. Epub 2010 Aug 4. Am J Physiol Cell Physiol. 2010. PMID: 20686069 Free PMC article.

10

Vulnerability of the cysteine-less proton-coupled folate transporter (PCFT-SLC46A1) to mutational stress associated with the substituted cysteine accessibility method.

Zhao R, Shin DS, Goldman ID. Zhao R, et al. Among authors: goldman id. Biochim Biophys Acta. 2011 Apr;1808(4):1140-5. doi: 10.1016/j.bbamem.2011.01.008. Epub 2011 Jan 20. Biochim Biophys Acta. 2011. PMID: 21256110 Free PMC article.

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