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English
"Devolution" of bipedality
scholarly article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
title
"Devolution" of bipedality
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
author
Kym M Boycott
series ordinal
2
object named as
Kym M Boycott
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
Jillian S Parboosingh
series ordinal
3
object named as
Jillian S Parboosingh
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
author name string
Joachim Herz
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
language of work or name
English
0 references
publication date
16 May 2008
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
volume
105
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
page(s)
E25
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
issue
21
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
cites work
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396673
retrieved
25 May 2018
Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396673
retrieved
25 May 2018
Unertan syndrome: a case series demonstrating human devolution
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396673
retrieved
25 May 2018
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396673
retrieved
25 May 2018
Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2396673
retrieved
25 May 2018
Identifiers
DOI
10.1073/PNAS.0802584105
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
ADS bibcode
2008PNAS..105E..25H
0 references
PMCID
2396673
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
PubMed ID
18487453
1 reference
stated in
Europe PubMed Central
PMCID
2396673
retrieved
17 November 2017
ResearchGate publication ID
5363958
0 references
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