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Journal Abstract Search
247 related items for PubMed ID: 22733820
1. A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency. Lasry I, Seo YA, Ityel H, Shalva N, Pode-Shakked B, Glaser F, Berman B, Berezovsky I, Goncearenco A, Klar A, Levy J, Anikster Y, Kelleher SL, Assaraf YG. J Biol Chem; 2012 Aug 24; 287(35):29348-61. PubMed ID: 22733820 [Abstract] [Full Text] [Related]
9. Compound heterozygous mutations in SLC30A2/ZnT2 results in low milk zinc concentrations: a novel mechanism for zinc deficiency in a breast-fed infant. Itsumura N, Inamo Y, Okazaki F, Teranishi F, Narita H, Kambe T, Kodama H. PLoS One; 2013 Aug 24; 8(5):e64045. PubMed ID: 23741301 [Abstract] [Full Text] [Related]
10. Transient neonatal zinc deficiency due to a new autosomal dominant mutation in gene SLC30A2 (ZnT-2). Lova Navarro M, Vera Casaño A, Benito López C, Fernández Ballesteros MD, Godoy Díaz DJ, Crespo Erchiga A, Romero Brufau S. Pediatr Dermatol; 2014 Aug 24; 31(2):251-2. PubMed ID: 24456035 [Abstract] [Full Text] [Related]
12. Histidine pairing at the metal transport site of mammalian ZnT transporters controls Zn2+ over Cd2+ selectivity. Hoch E, Lin W, Chai J, Hershfinkel M, Fu D, Sekler I. Proc Natl Acad Sci U S A; 2012 May 08; 109(19):7202-7. PubMed ID: 22529353 [Abstract] [Full Text] [Related]
13. Novel SLC30A2 mutations in the pathogenesis of transient neonatal zinc deficiency. Muto T, Kawase Y, Aiba K, Okuma M, Itsumura N, Luo S, Ogawa N, Tsuji T, Kambe T. Pediatr Investig; 2023 Mar 08; 7(1):6-12. PubMed ID: 36967740 [Abstract] [Full Text] [Related]
14. Molecular architecture and function of ZnT transporters. Kambe T. Curr Top Membr; 2012 Mar 08; 69():199-220. PubMed ID: 23046652 [Abstract] [Full Text] [Related]
15. Identification and cloning of a beta-cell-specific zinc transporter, ZnT-8, localized into insulin secretory granules. Chimienti F, Devergnas S, Favier A, Seve M. Diabetes; 2004 Sep 08; 53(9):2330-7. PubMed ID: 15331542 [Abstract] [Full Text] [Related]
16. Loss-of-function SLC30A2 mutants are associated with gut dysbiosis and alterations in intestinal gene expression in preterm infants. Kelleher SL, Alam S, Rivera OC, Barber-Zucker S, Zarivach R, Wagatsuma T, Kambe T, Soybel DI, Wright J, Lamendella R. Gut Microbes; 2022 Sep 08; 14(1):2014739. PubMed ID: 34965180 [Abstract] [Full Text] [Related]
17. Three-dimensional structure of beta-cell-specific zinc transporter, ZnT-8, predicted from the type 2 diabetes-associated gene variant SLC30A8 R325W. Weijers RN. Diabetol Metab Syndr; 2010 Jun 05; 2(1):33. PubMed ID: 20525392 [Abstract] [Full Text] [Related]
20. Zinc transport and the inhibition of the L-type calcium channel are two separable functions of ZnT-1. Shusterman E, Beharier O, Levy S, Zarivach R, Etzion Y, Campbell CR, Lee IH, Dinudom A, Cook DI, Peretz A, Katz A, Gitler D, Moran A. Metallomics; 2017 Mar 22; 9(3):228-238. PubMed ID: 28091657 [Abstract] [Full Text] [Related] Page: [Next] [New Search]