SLC12A3 gene

Known as: solute carrier family 12 member 3, TSC, NCCT 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1965-2018
020406019652018

Papers overview

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2011
2011
BACKGROUND AND OBJECTIVES Gitelman's syndrome (GS) is an autosomal recessive renal tubular disorder caused by mutations in the… (More)
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2008
2008
BACKGROUND AND PURPOSE Quantification of early ischemic changes (EIC) may predict functional outcome in patients with basilar… (More)
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2007
2007
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC12A3 gene that encodes the… (More)
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2007
2007
OBJECTIVES To correlate the two types of early ischemic change on noncontrast CT (NCCT) (parenchymal hypoattenuation [PH] and… (More)
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Highly Cited
2006
Highly Cited
2006
BACKGROUND AND PURPOSE We investigated whether computed tomography (CT) perfusion-derived cerebral blood flow (CBF) and cerebral… (More)
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2005
2005
OBJECTIVE To evaluate the usefulness of urinary calculi attenuation values from non-contrast computed tomography (NCCT) in… (More)
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2003
Highly Cited
2003
Mutations in the serine-threonine kinases WNK1 and WNK4 [with no lysine (K) at a key catalytic residue] cause… (More)
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Highly Cited
2002
Highly Cited
2002
PURPOSE Hypokalemic salt-losing tubulopathies (Bartter-like syndromes) comprise a set of clinically and genetically distinct… (More)
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Highly Cited
2001
Highly Cited
2001
The relationship between salt homeostasis and blood pressure has remained difficult to establish from epidemiological studies of… (More)
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Highly Cited
2000
Highly Cited
2000
OBJECTIVES Several investigators have evaluated noncontrast computed tomography (NCCT) in predicting stone composition in vitro… (More)
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