Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cellular expression and subcellular localization of the human Ins(1,3,4,5)P(4)-binding protein, p42(IP4), in human brain and in neuronal cells.

Brain research. Molecular brain research - 28 Feb 2002

Sedehizade Fariba, Hanck Theo, Stricker Rolf, Horstmayer Angelika, Bernstein Hans Gert, Reiser Georg

Abstract excerpt

In this study we describe for the human inositol-(1,3,4,5)-tetrakisphosphate (InsP4)-binding protein, p42IP4, the cellular distribution and subcellular localization in human brain and in transfected neuronal cells. The cDNA sequence of the human p42IP4 containing a single open reading frame yields a peptide of 374 amino acids with a calculated molecular mass of 43.4 kDa with a zinc-finger motif at the N-terminus,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Compartmentation
Share to CHO Cells

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cricetinae

Share to Inositol Phosphates

Share to Intracellular Membranes

Share to Receptors, Cytoplasmic and Nuclear

Share to Second Messenger Systems

Share to Zinc Fingers

Source

Identifiers

PMID: 11869802
DOI: 10.1016/s0169-328x(01)00335-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cellular expression and subcellular localization of the human Ins(1,3,4,5)P(4)-binding protein, p42(IP4), in human brain and in neuronal cells.PMID 11869802Read ↗

p42(IP4)/centaurin alpha1, a brain-specific PtdIns(3,4,5)P3/Ins(1,3,4,5)P4-binding protein: membrane trafficking induced by epidermal growth factor is inhibited by stimulation of phospholipase C-coupled thrombin receptor.Semantic proximity Read ↗

MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.Semantic proximity Read ↗

<i>MINPP1</i> prevents intracellular accumulation of the cation chelator inositol hexakisphosphate and is mutated in Pontocerebellar HypoplasiaSemantic proximity Read ↗

Novel PSI domains in plant and animal H+-inositol symporters.Semantic proximity Read ↗

The human homolog of the rat inositol phosphate multikinase is an inositol 1,3,4,6-tetrakisphosphate 5-kinase.Semantic proximity Read ↗

Evaluation of expression and function of the H+/myo-inositol transporter HMIT.Semantic proximity Read ↗

Phosphorylation of type-1 inositol 1,4,5-trisphosphate receptors by cyclic nucleotide-dependent protein kinases: a mutational analysis of the functionally important sites in the S2+ and S2- splice variants.Semantic proximity Read ↗

Role of Inositol 1,4,5-Trishosphate Receptors in Pathogenesis of Huntington’s Disease and Spinocerebellar AtaxiasSemantic proximity Read ↗

IMPA1 dependent regulation of plasma membrane phosphatidylinositol 4,5-bisphosphate turnover and calcium signalling by lithiumSemantic proximity Read ↗

Human 1-D-myo-inositol-3-phosphate synthase is functional in yeast.Semantic proximity Read ↗

Differences in both inositol 1,4,5-trisphosphate mass and inositol 1,4,5-trisphosphate receptors between normal and dystrophic skeletal muscle cell linesSemantic proximity Read ↗

Molecular modelling and site-directed mutagenesis of the inositol 1,3,4,5-tetrakisphosphate-binding pleckstrin homology domain from the Ras GTPase-activating protein GAP1IP4BP.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.