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SLC30A4 gene
Known as:
ZNT4
, SOLUTE CARRIER FAMILY 30 (ZINC TRANSPORTER), MEMBER 4
, SLC30A4
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Premutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding
E. Napoli
,
C. Ross-Inta
,
+6 authors
C. Giulivi
Frontiers in Neuroscience
2016
Corpus ID: 17961452
Fragile X premutation alleles have 55–200 CGG repeats in the 5′ UTR of the FMR1 gene. Altered zinc (Zn) homeostasis has been…
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2013
2013
Cooperative Functions of ZnT1, Metallothionein and ZnT4 in the Cytoplasm Are Required for Full Activation of TNAP in the Early Secretory Pathway
Shigeyuki Fujimoto
,
Naoya Itsumura
,
+8 authors
T. Kambe
PLoS ONE
2013
Corpus ID: 12630646
The activation process of secretory or membrane-bound zinc enzymes is thought to be a highly coordinated process involving zinc…
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2006
2006
Increased abundance of labile intracellular zinc during cell proliferation was due to increased retention of extracellular zinc in 3T3 cells.
M. Simpson
,
Zhaoming Xu
Journal of Nutritional Biochemistry
2006
Corpus ID: 28000701
2006
2006
The Znt4 mutation inlethal milk mice affects intestinal zinc homeostasis through the expression of other Zn transporters
C. Murgia
,
I. Vespignani
,
Rita Rami
,
G. Perozzi
Genes & Nutrition
2006
Corpus ID: 24176156
The lethal milk mouse syndrome is caused by a point mutation in the zinc transporter gene ZnT4 resulting in defective zinc…
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2004
2004
Expression profiles of zinc transporters in rodent placental models.
Nagayoshi Asano
,
M. Kondoh
,
+7 authors
Yoshiteru Watanabe
Toxicology Letters
2004
Corpus ID: 30291646
Highly Cited
2003
Highly Cited
2003
Analysis of zinc transporter, hZnT4 (Slc30A4), gene expression in a mammary gland disorder leading to reduced zinc secretion into milk
A. Michalczyk
,
G. Varigos
,
A. Catto-Smith
,
Rachael C. Blomeley
,
M. Ackland
Human Genetics
2003
Corpus ID: 36141272
Zinc deficiency, causing impaired growth and development, may have a nutritional or genetic basis. We investigated two cases of…
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2003
2003
Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15
S. Küry
,
C. Rubie
,
J. Moisan
,
G. Stöber
Journal of neural transmission
2003
Corpus ID: 26294057
Summary. The zinc transporter gene SLC30A4, located on chromosome 15q15-q21, has previously been reported to show altered…
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2001
2001
Expression pattern, genomic structure and evaluation of the human SLC30A4 gene as a candidate for acrodermatitis enteropathica
S. Küry
,
M. Devilder
,
H. Avet-Loiseau
,
B. Dréno
,
J. Moisan
Human Genetics
2001
Corpus ID: 11501283
Abstract. Slc30a4 is the fourth and last identified member of a mammalian proteins family presumably involved in the cellular…
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2001
2001
Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica
O. Bleck
,
G. Ashton
,
+5 authors
J. McGrath
Archives of Dermatological Research
2001
Corpus ID: 13027648
Abstract Acrodermatitis enteropathica is an inherited disorder of zinc metabolism, the molecular basis of which is currently…
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Highly Cited
1999
Highly Cited
1999
Cloning, expression, and vesicular localization of zinc transporter Dri 27/ZnT4 in intestinal tissue and cells.
C. Murgia
,
I. Vespignani
,
J. Cerase
,
F. Nobili
,
G. Perozzi
American Journal of Physiology - Gastrointestinal…
1999
Corpus ID: 4515441
We have identified the Dri 27 cDNA on the basis of its upregulated expression during rat intestinal development. It encodes a…
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