LIVIVO - Das Suchportal für Lebenswissenschaften

switch to English language
Erweiterte Suche

Ihre letzten Suchen

  1. TI=Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6 a new member of the TRPM gene family
  2. AU="Kilders, Valerie"

Suchergebnis

Treffer 1 - 1 von insgesamt 1

Suchoptionen

Artikel: Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

Schlingmann, Karl P / Weber, Stefanie / Peters, Melanie / Niemann Nejsum, Lene / Vitzthum, Helga / Klingel, Karin / Kratz, Markus / Haddad, Elie / Ristoff, Ellinor / Dinour, Dganit / Syrrou, Maria / Nielsen, Søren / Sassen, Martin / Waldegger, Siegfried / Seyberth, Hannsjörg W / Konrad, Martin

Nature genetics

2002  Band 31, Heft 2, Seite(n) 166–170

Abstract: ... previously mapped to chromosome 9q22 (ref. 3). The TRPM6 protein is a new member of the long ... encoding TRPM6, in autosomal-recessive hypomagnesemia with secondary hypocalcemia (HSH, OMIM 602014 ... transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein ...

Abstract Magnesium is an essential ion involved in many biochemical and physiological processes. Homeostasis of magnesium levels is tightly regulated and depends on the balance between intestinal absorption and renal excretion. However, little is known about specific proteins mediating transepithelial magnesium transport. Using a positional candidate gene approach, we identified mutations in TRPM6 (also known as CHAK2), encoding TRPM6, in autosomal-recessive hypomagnesemia with secondary hypocalcemia (HSH, OMIM 602014), previously mapped to chromosome 9q22 (ref. 3). The TRPM6 protein is a new member of the long transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein that combines calcium- and magnesium-permeable cation channel properties with protein kinase activity. TRPM6 is expressed in intestinal epithelia and kidney tubules. These findings indicate that TRPM6 is crucial for magnesium homeostasis and implicate a TRPM family member in human disease.
Mesh-Begriff(e) Adult ; Female ; Haplotypes ; Humans ; Hypocalcemia/etiology ; Hypocalcemia/genetics ; Infant ; Infant, Newborn ; Ion Channels/genetics ; Ion Channels/physiology ; Magnesium/blood ; Male ; Molecular Sequence Data ; Multigene Family/genetics ; Mutation ; Pedigree ; Sequence Analysis, DNA ; TRPM Cation Channels
Chemische Substanzen Ion Channels ; TRPM Cation Channels ; TRPM6 protein, human ; Magnesium (I38ZP9992A)
Sprache Englisch
Erscheinungsdatum 2002-06
Erscheinungsland United States
Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 1108734-1
ISSN 1546-1718 ; 1061-4036
ISSN (online) 1546-1718
ISSN 1061-4036
DOI 10.1038/ng889
Signatur
Zs.A 3613: Hefte anzeigen Standort:
Je nach Verfügbarkeit (siehe Angabe bei Bestand)
bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
Jg. 1995 - 2021: Lesesall (2.OG)
ab Jg. 2022: Lesesaal (EG)
Zs.MG 46: Hefte anzeigen
Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

Zusatzmaterialien

Kategorien

Zum Seitenanfang