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342 related items for PubMed ID: 25468189

  • 1. Genetic causes and gene–nutrient interactions in mammalian zinc deficiencies: acrodermatitis enteropathica and transient neonatal zinc deficiency as examples.
    Kasana S, Din J, Maret W.
    J Trace Elem Med Biol; 2015 Jan; 29():47-62. PubMed ID: 25468189
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  • 2. Overview of Inherited Zinc Deficiency in Infants and Children.
    Kambe T, Fukue K, Ishida R, Miyazaki S.
    J Nutr Sci Vitaminol (Tokyo); 2015 Jan; 61 Suppl():S44-6. PubMed ID: 26598882
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  • 3. 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 Jan; 31(2):251-2. PubMed ID: 24456035
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  • 4. The role of the zinc transporter SLC30A2/ZnT2 in transient neonatal zinc deficiency.
    Golan Y, Kambe T, Assaraf YG.
    Metallomics; 2017 Oct 18; 9(10):1352-1366. PubMed ID: 28665435
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  • 5. Acrodermatitis enteropathica and an overview of zinc metabolism.
    Maverakis E, Fung MA, Lynch PJ, Draznin M, Michael DJ, Ruben B, Fazel N.
    J Am Acad Dermatol; 2007 Jan 18; 56(1):116-24. PubMed ID: 17190629
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  • 6. 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 18; 80(4):586-94. PubMed ID: 27304099
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  • 7. A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica.
    Meftah SP, Kuivaniemi H, Tromp G, Kerkeni A, Sfar MT, Ayadi A, Prasad AS.
    Nutrition; 2006 Oct 18; 22(10):1067-70. PubMed ID: 16889938
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  • 10. The mouse acrodermatitis enteropathica gene Slc39a4 (Zip4) is essential for early development and heterozygosity causes hypersensitivity to zinc deficiency.
    Dufner-Beattie J, Weaver BP, Geiser J, Bilgen M, Larson M, Xu W, Andrews GK.
    Hum Mol Genet; 2007 Jun 15; 16(12):1391-9. PubMed ID: 17483098
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  • 11. 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 15; 29(6):556-561. PubMed ID: 32278324
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  • 12. Acrodermatitis enteropathica.
    Maverakis E, Lynch PJ, Fazel N.
    Dermatol Online J; 2007 Jul 13; 13(3):11. PubMed ID: 18328205
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  • 13. Acrodermatitis enteropathica mutations affect transport activity, localization and zinc-responsive trafficking of the mouse ZIP4 zinc transporter.
    Wang F, Kim BE, Dufner-Beattie J, Petris MJ, Andrews G, Eide DJ.
    Hum Mol Genet; 2004 Mar 01; 13(5):563-71. PubMed ID: 14709598
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  • 14. High proportion of transient neonatal zinc deficiency causing alleles in the general population.
    Golan Y, Lehvy A, Horev G, Assaraf YG.
    J Cell Mol Med; 2019 Feb 01; 23(2):828-840. PubMed ID: 30450693
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  • 15. The histidine-rich loop in the extracellular domain of ZIP4 binds zinc and plays a role in zinc transport.
    Zhang T, Kuliyev E, Sui D, Hu J.
    Biochem J; 2019 Jun 28; 476(12):1791-1803. PubMed ID: 31164399
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  • 16. 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 Jun 28; 8(5):e64045. PubMed ID: 23741301
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  • 17. One novel homozygous mutation of SLC39A4 gene in a Chinese patient with acrodermatitis enteropathica.
    Li CR, Yan SM, Shen DB, Li Q, Shao JP, Xue CY, Cao YH.
    Arch Dermatol Res; 2010 May 28; 302(4):315-7. PubMed ID: 20300938
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