(Q46602219)

23 December 2017

title

Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease (English)

1 reference

23 December 2017

8

Nobutaka Hattori

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23 December 2017

10

Yoshikuni Mizuno

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23 December 2017

3

Tomoko Toyota

1 reference

23 December 2017

Yoshimi Iwayama

4

object named as

Yoshimi Iwayama

1 reference

23 December 2017

Kazuo Yamada

2

object named as

Kazuo Yamada

1 reference

23 December 2017

author name string

Masayuki Ide

1

1 reference

23 December 2017

Yuichi Ishitsuka

5

1 reference

23 December 2017

Yoshio Minabe

6

1 reference

23 December 2017

Kazuhiko Nakamura

7

1 reference

23 December 2017

Takashi Asada

9

1 reference

23 December 2017

Norio Mori

11

1 reference

23 December 2017

Takeo Yoshikawa

12

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23 December 2017

publication date

14 July 2005

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23 December 2017

published in

Human Genetics

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23 December 2017

volume

117

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23 December 2017

issue

6

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23 December 2017

page(s)

520-527

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23 December 2017

https://scigraph.springernature.com/pub.10.1007/s00439-005-1342-8

exact match

0 references

cites work

Risk of Parkinson's disease among first-degree relatives: A community-based study

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-005-1342-8

Specification of the central noradrenergic phenotype by the homeobox gene Phox2b.

21 January 2018

1 reference

12 December 2020

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

12 December 2020

Notch signaling induces rapid degradation of achaete-scute homolog 1.

1 reference

12 December 2020

Parkinson's disease: piecing together a genetic jigsaw

1 reference

12 December 2020

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

12 December 2020

Genetic and environmental factors in the cause of Parkinson's disease

1 reference

12 December 2020

Neuronal loss is greater in the locus coeruleus than nucleus basalis and substantia nigra in Alzheimer and Parkinson diseases

1 reference

12 December 2020

Localization of the human achaete-scute homolog gene (ASCL1) distal to phenylalanine hydroxylase (PAH) and proximal to tumor rejection antigen (TRA1) on chromosome 12q22-q23

1 reference

12 December 2020

Mechanisms of cell death in polyglutamine expansion diseases

1 reference

12 December 2020

Locus coeruleus lesions potentiate neurotoxic effects of MPTP in dopaminergic neurons of the substantia nigra

1 reference

12 December 2020

The role of the locus coeruleus in the development of Parkinson's disease

1 reference

12 December 2020

Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene

1 reference

12 December 2020

Effects of noradrenergic lesions on MPTP/MPP+ kinetics and MPTP-induced nigrostriatal dopamine depletions.

1 reference

12 December 2020

Treatment with alpha2-adrenoceptor antagonist, 2-methoxy idazoxan, protects 6-hydroxydopamine-induced Parkinsonian symptoms in rats: neurochemical and behavioral evidence

1 reference

12 December 2020

Neural networks and disease association studies.

1 reference

12 December 2020

Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B.

1 reference

12 December 2020

Effects of locus coeruleus lesions on parkinsonian signs, striatal dopamine and substantia nigra cell loss after 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in monkeys: a possible role for the locus coeruleus in the progression of Parkinson's disea

1 reference

12 December 2020

Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis

1 reference

12 December 2020

Familial Parkinson's disease: a hint to elucidate the mechanisms of nigral degeneration

1 reference

12 December 2020

Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping

1 reference

12 December 2020

A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia

1 reference

12 December 2020

Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)

1 reference

12 December 2020

The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

1 reference

12 December 2020

10.1007/S00439-005-1342-8

Identifiers

DOI

1 reference

23 December 2017

PubMed ID

16021468

1 reference

23 December 2017