Association of transcription factor gene LMX1B with autism (Q34013736)

30 July 2017

Association of transcription factor gene LMX1B with autism (English)

1 reference

30 July 2017

0 references

7

Tomoko Toyota

1 reference

30 July 2017

6

Yoshimi Iwayama

1 reference

30 July 2017

5

Kazuo Yamada

1 reference

30 July 2017

Ismail Thanseem

1

1 reference

30 July 2017

Kazuhiko Nakamura

2

1 reference

30 July 2017

Ayyappan Anitha

3

1 reference

30 July 2017

Shiro Suda

4

1 reference

30 July 2017

Masatsugu Tsujii

8

1 reference

30 July 2017

Yasuhide Iwata

9

1 reference

30 July 2017

Katsuaki Suzuki

10

1 reference

30 July 2017

Hideo Matsuzaki

11

1 reference

30 July 2017

Keiko Iwata

12

1 reference

30 July 2017

Toshiro Sugiyama

13

1 reference

30 July 2017

Takeo Yoshikawa

14

1 reference

30 July 2017

Norio Mori

15

1 reference

30 July 2017

language of work or name

English

0 references

publication date

25 August 2011

1 reference

30 July 2017

1 reference

30 July 2017

6

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30 July 2017

e23738

1 reference

30 July 2017

8

1 reference

Creative Commons Attribution 4.0 International

30 July 2017

start time

25 August 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Adult raphe-specific deletion of Lmx1b leads to central serotonin deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Prevalence and interpretation of recent trends in rates of pervasive developmental disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Brain serotonin and dopamine transporter bindings in adults with high-functioning autism.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Lmx1b is required for maintenance of central serotonergic neurons and mice lacking central serotonergic system exhibit normal locomotor activity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Selective serotonin reuptake inhibitors in autism: a review of efficacy and tolerability.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Lmx1b is essential for the development of serotonergic neurons

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

High-throughput genotyping with single nucleotide polymorphisms

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Molecular models for vertebrate limb development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Anterior cingulate gyrus volume and glucose metabolism in autistic disorder.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

The serotonin system in autism

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

5 July 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Effects of tryptophan depletion in drug-free adults with autistic disorder.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Autism as a strongly genetic disorder: evidence from a British twin study

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

5 July 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Serotonin transporter promoter variants in autism: functional effects and relationship to platelet hyperserotonemia

5 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Significance of abnormalities in developmental trajectory and asymmetry of cortical serotonin synthesis in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Serotonin and dopamine transporter binding in children with autism determined by SPECT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Preliminary evidence that polymorphisms in dopamine-related transcription factors LMX1A, LMX1B and PITX3 are associated with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Complementary roles for Nkx6 and Nkx2 class proteins in the establishment of motoneuron identity in the hindbrain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Abnormal regional cerebral blood flow in childhood autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

A spectrum of LMX1B mutations in Nail-Patella syndrome: New point mutations, deletion, and evidence of mosaicism in unaffected parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Forced Expression of LIM Homeodomain Transcription Factor 1b Enhances Differentiation of Mouse Embryonic Stem Cells into Serotonergic Neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023738

Lmx1b, Pet-1, andNkx2.2Coordinately Specify Serotonergic Neurotransmitter Phenotype

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3162001

Nail-patella syndrome: identification of mutations in the LMX1B gene in Dutch families

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21901133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0023738

1 reference

30 July 2017

0 references

1 reference

30 July 2017

1 reference