(Q28587473)

Membrane magnesium transporter 1

GOA release 2020-03-11

1 reference

American Journal of Physiology - Cell Physiology

GOA release 2020-03-11

author name string

Angela Goytain

series ordinal

1

1 reference

31 January 2017

Gary A. Quamme

series ordinal

2

1 reference

31 January 2017

1 February 2008

1 reference

31 January 2017

1 reference

31 January 2017

294

1 reference

31 January 2017

C495–502

1 reference

31 January 2017

2

1 reference

31 January 2017

Chloride channels of intracellular organelles.

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

The yeast mutant vps5Delta affected in the recycling of Golgi membrane proteins displays an enhanced vacuolar Mg2+/H+ exchange activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Magnesium transport in the renal distal convoluted tubule

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Magnesium transport across cell membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Functional characterization of human SLC41A1, a Mg2+ transporter with similarity to prokaryotic MgtE Mg2+ transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Identification and characterization of a novel mammalian Mg2+ transporter with channel-like properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Functional characterization of ACDP2 (ancient conserved domain protein), a divalent metal transporter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

TRPM8-independent menthol-induced Ca2+ release from endoplasmic reticulum and Golgi

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Ca2+ microdomains in smooth muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Calcium in the Golgi apparatus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

LTRPC7 is a Mg.ATP-regulated divalent cation channel required for cell viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Identification of a novel chloride channel expressed in the endoplasmic reticulum, golgi apparatus, and nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

The Mg2+ and Mg(2+)-nucleotide-regulated channel-kinase TRPM7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Immunomagnetic separation, primary culture, and characterization of cortical thick ascending limb plus distal convoluted tubule cells from mouse kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Renal magnesium handling: new insights in understanding old problems

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Dynamics of intracellular free Mg2+ changes in a vascular smooth muscle cell line

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Anion channels transport ATP into the Golgi lumen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Magnesium in clinical medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Construction of a physical and transcript map for a 1-Mb genomic region containing the urofacial (Ochoa) syndrome gene on 10q23-q24 and localization of the disease gene within two overlapping BAC clones (<360 kb).

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Potassium, magnesium, and electrolyte imbalance and complications in disease management.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

Localization of pore-forming subunit of the ATP-sensitive K(+)-channel, Kir6.2, in rat brain neurons and glial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00238.2007

10.1152/AJPCELL.00238.2007

21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

release_2svh5dl325ettaerqvp4lpn6oy

756022

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2svh5dl325ettaerqvp4lpn6oy

mapped directly with Wikidata item

24 November 2022

based on heuristic

756022

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference