Altered expression of two zinc transporters, SLC30A5 and SLC30A6, underlies a mammary gland disorder of reduced zinc secretion into milk-Reference-Cited by-同舟云学术

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Altered expression of two zinc transporters, SLC30A5 and SLC30A6, underlies a mammary gland disorder of reduced zinc secretion into milk

Published:2015-08-29 Issue:5 Volume:10 Page:
ISSN:1555-8932
Container-title:Genes & Nutrition
language:en
Short-container-title:Genes Nutr

Author:

Kumar Loveleen,Michalczyk Agnes,McKay Jill,Ford Dianne,Kambe Taiho,Hudek Lee,Varigios George,Taylor Philip E.,Ackland M. Leigh

Funder

Australian Research Council

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/s12263-015-0487-x.pdf

Reference38 articles.

1. Ackland ML, Mercer JF (1992) The murine mutation, lethal milk, results in production of zinc-deficient milk. J Nutr 122:1214–1218

2. Aggett PJ, Atherton DJ, More J, Davey J, Delves HT, Harries JT (1980) Symptomatic zinc deficiency in a breast-fed preterm infant. Arch Dis Child 55:547–550

3. Bye AM, Goodfellow A, Atherton DJ (1985) Transient zinc deficiency in a full-term breast-fed infant of normal birth weight. Pediatr Dermatol 2:308–311

4. Chowanadisai W, Lönnerdal B, Kelleher SL (2006) Identification of a mutation in SLC30A2 (ZnT-2) in women with low milk zinc concentration that results in transient neonatal zinc deficiency. J Biol Chem 281:39699–39707. doi: 10.1074/jbc.M605821200

5. Connors TJ, Czarnecki DB, Haskett MI (1983) Acquired zinc deficiency in a breast-fed premature infant. Arch Dermatol 119:319–321

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1. Genome-Wide Association Studies and Runs of Homozygosity to Identify Reproduction-Related Genes in Yorkshire Pig Population;Genes;2023-11-27

2. Association of zinc level with DNA methylation and its consequences: A systematic review;Heliyon;2022-10

3. References;Breastfeeding;2022

4. Zinc Signaling in the Mammary Gland: For Better and for Worse;Biomedicines;2021-09-12

5. Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy;European Journal of Human Genetics;2021-02-05

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