Functional characterization of NIPA2, a selective Mg2 transporter (Q28507256)

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

title

Functional characterization of NIPA2, a selective Mg2 transporter (English)

2 references

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

Non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human)

11 January 2020

main subject

1 reference

NIPA-like domain containing 4

GOA release 2020-03-11

1 reference

NIPA-like domain containing 1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Rochelle Hines

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

author name string

Angela Goytain

series ordinal

1

2 references

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

Gary A Quamme

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

publication date

30 July 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

American Journal of Physiology - Cell Physiology

11 January 2020

published in

2 references

24 January 2017

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11 January 2020

volume

295

2 references

24 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

issue

4

2 references

24 January 2017

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11 January 2020

page(s)

C944-53

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

11 January 2020

cites work

1 reference

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Prader-Willi syndrome: current understanding of cause and diagnosis

21 January 2018

1 reference

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Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

21 January 2018

1 reference

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Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons

21 January 2018

1 reference

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Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families

21 January 2018

1 reference

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Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

21 January 2018

1 reference

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Intracellular Mg2 and magnesium depletion in isolated renal thick ascending limb cells

21 January 2018

1 reference

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Magnesium transport in the renal distal convoluted tubule

21 January 2018

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The hereditary spastic paraplegias: nine genes and counting

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Functional characterization of the mouse [corrected] solute carrier, SLC41A2

21 January 2018

1 reference

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

21 January 2018

1 reference

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Identification and characterization of a novel family of membrane magnesium transporters, MMgT1 and MMgT2

21 January 2018

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Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

21 January 2018

1 reference

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Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Renal magnesium handling: New insights in understanding old problems

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Mrs2p forms a high conductance Mg2 selective channel in mitochondria.

21 January 2018

1 reference

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TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism

21 January 2018

1 reference

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Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive

21 January 2018

1 reference

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A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152/AJPCELL.00091.2008

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/AJPCELL.00091.2008

10.1152/AJPCELL.00091.2008

21 January 2018

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18667602 AND SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017