NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
about
Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic developmentHuntingtin-interacting proteins, HIP14 and HIP14L, mediate dual functions, palmitoyl acyltransferase and Mg2+ transportSpastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretionGolgi-specific DHHC zinc finger protein GODZ mediates membrane Ca2+ transportProton-pump inhibitor-induced hypomagnesemia: Current research and proposed mechanismsThe 15q11.2 BP1-BP2 microdeletion syndrome: a reviewSLC41A1 is a novel mammalian Mg2+ carrierFunctional characterization of NIPA2, a selective Mg2+ transporterIdentification and characterization of a novel family of membrane magnesium transporters, MMgT1 and MMgT2Genetic variations in magnesium-related ion channels may affect diabetes risk among African American and Hispanic American womenSolute Carrier Family SLC41, what do we really know about it?Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanismspict, a cyst cell-specific gene, regulates starvation-induced spermatogonial cell death in the Drosophila testis.The effect of HSP-causing mutations in SPG3A and NIPA1 on the assembly, trafficking, and interaction between atlastin-1 and NIPA1Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.Cellular magnesium homeostasis.Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly.Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy.Genetic diversity of Trichoderma atroviride strains collected in Poland and identification of loci useful in detection of within-species diversity.'Lemonade Legs': Why do Some Patients Get Profound Hypomagnesaemia on Proton-Pump Inhibitors?Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature.Gene Expression Profiling of Tuberculous Meningitis Co-infected with HIVRare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese populationGem-1 encodes an SLC16 monocarboxylate transporter-related protein that functions in parallel to the gon-2 TRPM channel during gonad development in Caenorhabditis elegans.Aldosterone Upregulates Transient Receptor Potential Melastatin 7 (TRPM7).The unique nature of mg2+ channels.Identification and proximal tubular localization of the Mg²⁺ transporter, Slc41a1, in a seawater fish.Molecular identification of ancient and modern mammalian magnesium transporters.Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases.Hereditary spastic paraplegias: membrane traffic and the motor pathway.Cellular pathways of hereditary spastic paraplegia.A pharmacogenetic study of docetaxel and thalidomide in patients with castration-resistant prostate cancer using the DMET genotyping platform.Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders.The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling.Mrs2p forms a high conductance Mg2+ selective channel in mitochondria.Genetic and morphological features of human iPSC-derived neurons with chromosome 15q11.2 (BP1-BP2) deletionsPathogenesis of autosomal dominant hereditary spastic paraplegia (SPG6) revealed by a rat model.Identification of a new host factor required for antiviral RNAi and amplification of viral siRNAs.
P2860
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P2860
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
description
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 2007
@ast
im März 2007 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2007/03/16)
@sk
vědecký článek publikovaný v roce 2007
@cs
wetenschappelijk artikel (gepubliceerd op 2007/03/16)
@nl
наукова стаття, опублікована в березні 2007
@uk
name
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@ast
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@en
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@nl
type
label
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@ast
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@en
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@nl
prefLabel
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@ast
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@en
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@nl
P2093
P2860
P3181
P356
P1476
NIPA1(SPG6), the basis for aut ...... a functional Mg2+ transporter
@en
P2093
Alaa El-Husseini
Angela Goytain
Gary A Quamme
P2860
P304
P3181
P356
10.1074/JBC.M610314200
P407
P577
2006-12-13T00:00:00Z