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181 related items for PubMed ID: 27304099
1. Novel mutations in SLC30A2 involved in the pathogenesis of transient neonatal zinc deficiency. Itsumura N, Kibihara Y, Fukue K, Miyata A, Fukushima K, Tamagawa-Mineoka R, Katoh N, Nishito Y, Ishida R, Narita H, Kodama H, Kambe T. Pediatr Res; 2016 Oct; 80(4):586-94. PubMed ID: 27304099 [Abstract] [Full Text] [Related]
5. A novel homozygous mutation p.E88K in maternal SLC30A2 gene as a cause of transient neonatal zinc deficiency. Li Z, Wang J, Yang Y, Wang S. Exp Dermatol; 2020 Jun; 29(6):556-561. PubMed ID: 32278324 [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 Dec; 31(2):251-2. PubMed ID: 24456035 [Abstract] [Full Text] [Related]
15. 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 Dec; 14(1):2014739. PubMed ID: 34965180 [Abstract] [Full Text] [Related]
16. Identification of a mutation in SLC30A2 (ZnT-2) in women with low milk zinc concentration that results in transient neonatal zinc deficiency. Chowanadisai W, Lönnerdal B, Kelleher SL. J Biol Chem; 2006 Dec 22; 281(51):39699-707. PubMed ID: 17065149 [Abstract] [Full Text] [Related]
18. A genetic variant in SLC30A2 causes breast dysfunction during lactation by inducing ER stress, oxidative stress and epithelial barrier defects. Lee S, Zhou Y, Gill DL, Kelleher SL. Sci Rep; 2018 Feb 23; 8(1):3542. PubMed ID: 29476070 [Abstract] [Full Text] [Related]