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Lethal milk mutation results in dietary zinc deficiency in nursing mice.

作者信息

Piletz J A, Ganschow R E

出版信息

Am J Clin Nutr. 1978 Apr;31(4):560-2. doi: 10.1093/ajcn/31.4.560.

DOI:10.1093/ajcn/31.4.560
PMID:637030
Abstract
摘要

相似文献

1
Lethal milk mutation results in dietary zinc deficiency in nursing mice.致死性乳突变导致哺乳小鼠出现膳食锌缺乏。
Am J Clin Nutr. 1978 Apr;31(4):560-2. doi: 10.1093/ajcn/31.4.560.
2
Zinc deficiency in murine milk underlies expression of the lethal milk (lm) mutation.小鼠乳汁中的锌缺乏是致死性乳汁(lm)突变表达的基础。
Science. 1978 Jan 13;199(4325):181-3. doi: 10.1126/science.619449.
3
The murine mutation, lethal milk, results in production of zinc-deficient milk.
J Nutr. 1992 Jun;122(6):1214-8. doi: 10.1093/jn/122.6.1214.
4
Altered zinc metabolism occurs in murine lethal milk syndrome.锌代谢改变发生在小鼠致死性乳综合征中。
J Nutr. 1992 Nov;122(11):2233-8. doi: 10.1093/jn/122.11.2233.
5
Acrodermatitis in breast-fed premature infants: evidence for a defect of mammary zinc secretion.母乳喂养早产儿的肢端皮炎:乳腺锌分泌缺陷的证据。
Pediatrics. 1982 Feb;69(2):176-83.
6
Zinc and copper in milk and tissues of nursing lethal milk mutant mice.
J Nutr. 1987 Jan;117(1):83-90. doi: 10.1093/jn/117.1.83.
7
Zinc metabolism in lethal-milk mice. Otolith, lactation, and aging effects.
J Hered. 1984 Nov-Dec;75(6):480-4. doi: 10.1093/oxfordjournals.jhered.a109990.
8
The mouse acrodermatitis enteropathica gene Slc39a4 (Zip4) is essential for early development and heterozygosity causes hypersensitivity to zinc deficiency.小鼠肠病性肢端皮炎基因Slc39a4(Zip4)对早期发育至关重要,杂合性会导致对锌缺乏高度敏感。
Hum Mol Genet. 2007 Jun 15;16(12):1391-9. doi: 10.1093/hmg/ddm088. Epub 2007 May 4.
9
A diagnostic challenge: a case of acrodermatitis enteropathica without hypozincemia and with maternal milk of low zinc level.一个诊断难题:一例无低锌血症且母乳锌水平低的肠病性肢端皮炎病例。
Pediatr Dermatol. 2010 Sep-Oct;27(5):534-5. doi: 10.1111/j.1525-1470.2010.01268.x. Epub 2010 Aug 27.
10
Transient symptomatic zinc deficiency in a breast-fed infant: relevance of a genetic study.母乳喂养婴儿一过性症状性锌缺乏症:基因研究的相关性。
Nutrition. 2011 Oct;27(10):1087-9. doi: 10.1016/j.nut.2011.06.002.

引用本文的文献

1
ZnT4 (SLC30A4)-null ("lethal milk") mice have defects in mammary gland secretion and hallmarks of precocious involution during lactation.锌转运蛋白4(SLC30A4)基因敲除的(“致死性乳汁”)小鼠存在乳腺分泌缺陷以及泌乳期间过早退化的特征。
Am J Physiol Regul Integr Comp Physiol. 2016 Jan 1;310(1):R33-40. doi: 10.1152/ajpregu.00315.2014. Epub 2015 Nov 4.
2
SLC30A10: A novel manganese transporter.溶质载体家族30成员10:一种新型锰转运体。
Worm. 2015 May 11;4(3):e1042648. doi: 10.1080/21624054.2015.1042648. eCollection 2015 Jul-Sep.
3
Exome Sequencing of SLC30A2 Identifies Novel Loss- and Gain-of-Function Variants Associated with Breast Cell Dysfunction.
SLC30A2的外显子测序鉴定出与乳腺细胞功能障碍相关的新型功能丧失和功能获得变异体。
J Mammary Gland Biol Neoplasia. 2015 Dec;20(3-4):159-72. doi: 10.1007/s10911-015-9338-z. Epub 2015 Aug 21.
4
Genome wide identification, phylogeny and expression of zinc transporter genes in common carp.鲤鱼锌转运蛋白基因的全基因组鉴定、系统发育及表达分析
PLoS One. 2014 Dec 31;9(12):e116043. doi: 10.1371/journal.pone.0116043. eCollection 2014.
5
ZnT4 provides zinc to zinc-dependent proteins in the trans-Golgi network critical for cell function and Zn export in mammary epithelial cells.锌转运蛋白 4 在反式高尔基体网络中为锌依赖性蛋白提供锌,这对乳腺上皮细胞的细胞功能和锌输出至关重要。
Am J Physiol Cell Physiol. 2012 Aug 1;303(3):C291-7. doi: 10.1152/ajpcell.00443.2011. Epub 2012 May 23.
6
Zinc transfer to the breastfed infant.锌向母乳喂养婴儿的转移。
J Mammary Gland Biol Neoplasia. 1999 Jul;4(3):259-68. doi: 10.1023/a:1018797829351.
7
Induction of metallothionein by zinc in lethal milk mutant mice.锌对致死性乳突变小鼠金属硫蛋白的诱导作用。
Biochem Genet. 1982 Dec;20(11-12):1221-33. doi: 10.1007/BF00498945.
8
Zinc metabolism in animals: pathology, immunology and genetics.动物体内的锌代谢:病理学、免疫学与遗传学
J Inherit Metab Dis. 1983;6 Suppl 1:34-8. doi: 10.1007/BF01811321.
9
Intestinal metallothionein in lethal-milk mice with systemic zinc deficiency.
Biochem Genet. 1986 Aug;24(7-8):635-42. doi: 10.1007/BF00504340.