Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2001-5-30
pubmed:abstractText
A new protein, named paracellin 1 (PCLN-1), expressed in human thick ascending limb (TAL) tight junctions, possibly plays a critical role in the control of magnesium and calcium reabsorption, since mutations of PCLN-1 are present in the hypomagnesemia hypercalciuria syndrome (HHS). However, no functional experiments have demonstrated that TAL magnesium and calcium reabsorption were actually impaired in patients with HHS.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0085-2538
pubmed:author
pubmed:issnType
Print
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2206-15
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11380823-Adolescent, pubmed-meshheading:11380823-Adult, pubmed-meshheading:11380823-Calcium, pubmed-meshheading:11380823-Cations, Divalent, pubmed-meshheading:11380823-Child, pubmed-meshheading:11380823-Diuretics, pubmed-meshheading:11380823-Family Health, pubmed-meshheading:11380823-Female, pubmed-meshheading:11380823-Furosemide, pubmed-meshheading:11380823-Genotype, pubmed-meshheading:11380823-Homozygote, pubmed-meshheading:11380823-Humans, pubmed-meshheading:11380823-Loop of Henle, pubmed-meshheading:11380823-Magnesium Chloride, pubmed-meshheading:11380823-Male, pubmed-meshheading:11380823-Membrane Proteins, pubmed-meshheading:11380823-Middle Aged, pubmed-meshheading:11380823-Natriuresis, pubmed-meshheading:11380823-Nephrocalcinosis, pubmed-meshheading:11380823-Pedigree, pubmed-meshheading:11380823-Phenotype, pubmed-meshheading:11380823-Point Mutation, pubmed-meshheading:11380823-Sodium Chloride
pubmed:year
2001
pubmed:articleTitle
Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle.
pubmed:affiliation
Département de Physiologie et Radio-Isotopes, Université Pierre et Marie Curie, INSERM U356, Institut Fédératif de Recherche 58, Laboratoire de Génétique Moléculaire, Hôpital Universitaire Européen Georges Pompidou, Paris, France. blanch@ccr.jussieu.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't