A new syndrome with quadrupedal gait, primitive speech, and severe mental retardation as a live model for human evolution
about
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTwo families with quadrupedalism, mental retardation, no speech, and infantile hypotonia (Uner Tan Syndrome Type-II); a novel theory for the evolutionary emergence of human bipedalism.Human quadrupeds, primate quadrupedalism, and Uner Tan SyndromeUnertan syndrome: a case series demonstrating human devolutionUner tan syndrome: history, clinical evaluations, genetics, and the dynamics of human quadrupedalismEvidence for "Unertan Syndrome" and the evolution of the human mind.Unertan syndrome: review and report of four new cases.Preclinical evidence supporting the clinical development of central pattern generator-modulating therapies for chronic spinal cord-injured patients.Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.The very low density lipoprotein receptor-associated pontocerebellar hypoplasia and dysmorphic features in three Turkish patientsCharacterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ).Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotionCentral pattern generator for locomotion: anatomical, physiological, and pathophysiological considerations.The neural control of interlimb coordination during mammalian locomotion.A wrist-walker exhibiting no "Uner Tan Syndrome": a theory for possible mechanisms of human devolution toward the atavistic walking patterns.WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.Evidence for "Uner Tan Syndrome" as a human model for reverse evolution."Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scans.A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof-of-concept examples.
P2860
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P2860
A new syndrome with quadrupedal gait, primitive speech, and severe mental retardation as a live model for human evolution
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
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2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年论文
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name
A new syndrome with quadrupeda ...... live model for human evolution
@ast
A new syndrome with quadrupeda ...... live model for human evolution
@en
A new syndrome with quadrupeda ...... live model for human evolution
@nl
type
label
A new syndrome with quadrupeda ...... live model for human evolution
@ast
A new syndrome with quadrupeda ...... live model for human evolution
@en
A new syndrome with quadrupeda ...... live model for human evolution
@nl
prefLabel
A new syndrome with quadrupeda ...... live model for human evolution
@ast
A new syndrome with quadrupeda ...... live model for human evolution
@en
A new syndrome with quadrupeda ...... live model for human evolution
@nl
P1476
A new syndrome with quadrupeda ...... live model for human evolution
@en
P2093
P356
10.1080/00207450500455330
P407
P577
2006-03-01T00:00:00Z