(Q22007950)

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Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA)

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Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA) (English)

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Bassoon presynaptic cytomatrix protein

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GOA release 2020-03-11

neurodegeneration

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inferred from title

multiple system atrophy

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author name string

H Hashida

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author given names

H

author last names

Hashida

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7 February 2023

J Goto

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author given names

J

author last names

Goto

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7 February 2023

N Zhao

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author given names

N

author last names

Zhao

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7 February 2023

N Takahashi

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author given names

N

author last names

Takahashi

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7 February 2023

M Hirai

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author given names

M

author last names

Hirai

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7 February 2023

I Kanazawa

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author given names

I

author last names

Kanazawa

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7 February 2023

Y Sakaki

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author given names

Y

author last names

Sakaki

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7 February 2023

language of work or name

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publication date

15 November 1998

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54

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1

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50-8

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A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study

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Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Immunocytochemical and ultrastructural studies of neuronal and oligodendroglial cytoplasmic inclusions in multiple system atrophy. 2. Oligodendroglial cytoplasmic inclusions

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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Environmental— occupational risk factors and familial associations in multiple system atrophy: A preliminary investigation

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome).

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy

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Transcriptional and posttranscriptional regulation of interferon-induced gene expression in human cells

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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A novel cysteine-rich sequence motif

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Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: identification of a class of bipartite nuclear targeting sequence

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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The LIM domain is a modular protein-binding interface

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Structural basis for the binding of proline-rich peptides to SH3 domains

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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High-density cDNA filter analysis: a novel approach for large-scale, quantitative analysis of gene expression

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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High-density cDNA filter analysis of the expression profiles of the genes preferentially expressed in human brain

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Initiation codons within 5'-leaders of mRNAs as regulators of translation

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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The PHD finger: implications for chromatin-mediated transcriptional regulation

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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The role of the leucine zipper in the fos-jun interaction

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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based on heuristic

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Porcine diacylglycerol kinase sequence has zinc finger and E-F hand motifs.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Novel cysteine-rich motif and homeodomain in the product of the Caenorhabditis elegans cell lineage gene lin-11.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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EEA1, an early endosome-associated protein. EEA1 is a conserved alpha-helical peripheral membrane protein flanked by cysteine "fingers" and contains a calmodulin-binding IQ motif

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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Noc2, a putative zinc finger protein involved in exocytosis in endocrine cells

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

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A novel cysteine-rich sequence-specific DNA-binding protein interacts with the conserved X-box motif of the human major histocompatibility complex class II genes via a repeated Cys-His domain and functions as a transcriptional repressor

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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based on heuristic

inferred from DOI database lookup

The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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based on heuristic

inferred from DOI database lookup

Degenerative diseases of the nervous system associated with autonomic failure

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Sequences 5' of the first upstream open reading frame in GCN4 mRNA are required for efficient translational reinitiation.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

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based on heuristic

inferred from DOI database lookup

Human TAF(II)135 potentiates transcriptional activation by the AF-2s of the retinoic acid, vitamin D3, and thyroid hormone receptors in mammalian cells

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Two binding orientations for peptides to the Src SH3 domain: development of a general model for SH3-ligand interactions

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Rabphilin-3A, a putative target protein for smg p25A/rab3A p25 small GTP-binding protein related to synaptotagmin

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration

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https://api.crossref.org/works/10.1006%2FGENO.1998.5516

7 January 2021

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Identifiers

10.1006/GENO.1998.5516

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