Literature DB >> 18487453

"Devolution" of bipedality.

Joachim Herz, Kym M Boycott, Jillian S Parboosingh.   

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Year:  2008        PMID： 18487453      PMCID： PMC2396673          DOI： 10.1073/pnas.0802584105

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  5 in total

1.  Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification.

Authors:  Kym M Boycott; Shauna Flavelle; Alexandre Bureau; Hannah C Glass; T Mary Fujiwara; Elaine Wirrell; Krista Davey; Albert E Chudley; James N Scott; D Ross McLeod; Jillian S Parboosingh
Journal:  Am J Hum Genet       Date:  2005-07-22       Impact factor: 11.025

2.  Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2.

Authors:  M Trommsdorff; M Gotthardt; T Hiesberger; J Shelton; W Stockinger; J Nimpf; R E Hammer; J A Richardson; J Herz
Journal:  Cell       Date:  1999-06-11       Impact factor: 41.582

3.  Unertan syndrome: a case series demonstrating human devolution.

Authors:  Uner Tan; Sibel Karaca; Meliha Tan; Bekir Yilmaz; Namik Kemal Bagci; Ayhan Ozkur; Sadrettin Pence
Journal:  Int J Neurosci       Date:  2008-01       Impact factor: 2.292

4.  Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome.

Authors:  Lia Abbasi Moheb; Andreas Tzschach; Masoud Garshasbi; Kimia Kahrizi; Hossein Darvish; Yaser Heshmati; Alireza Kordi; Hossein Najmabadi; Hans Hilger Ropers; Andreas Walter Kuss
Journal:  Eur J Hum Genet       Date:  2007-11-28       Impact factor: 4.246

5.  Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.

Authors:  Tayfun Ozcelik; Nurten Akarsu; Elif Uz; Safak Caglayan; Suleyman Gulsuner; Onur Emre Onat; Meliha Tan; Uner Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-07       Impact factor: 11.205
  5 in total
  10 in total

1.  Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion.

Authors:  Tayfun Ozcelik; Nurten Akarsu; Elif Uz; Safak Caglayan; Suleyman Gulsuner; Onur Emre Onat; Meliha Tan; Uner Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2008-06-10       Impact factor: 11.205

2.  Two Indian Families with Quadrupedal Locomotion Resembling Uner Tan Syndrome: A Video Document.

Authors:  Gurusidheshwar Wali
Journal:  Mov Disord Clin Pract       Date:  2016-06-06

3.  Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Authors:  Luis E Kolb; Zulfikar Arlier; Cengiz Yalcinkaya; Ali K Ozturk; Jennifer A Moliterno; Ozdem Erturk; Fatih Bayrakli; Baris Korkmaz; Michael L DiLuna; Katsuhito Yasuno; Kaya Bilguvar; Tayfun Ozcelik; Beyhan Tuysuz; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2010-01-15       Impact factor: 2.660

4.  A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins.

Authors:  Keiko Sakai; Oliver Tiebel; M Cecilia Ljungberg; Merry Sullivan; Hye-Jeong Lee; Tomoya Terashima; Rongying Li; Kunihisa Kobayashi; Hui-Chen Lu; Lawrence Chan; Kazuhiro Oka
Journal:  Brain Res       Date:  2009-04-22       Impact factor: 3.252

Review 5.  Apolipoprotein E receptors in the nervous system.

Authors:  Joachim Herz
Journal:  Curr Opin Lipidol       Date:  2009-06       Impact factor: 4.776

6.  Mutations in VLDLR as a cause for autosomal recessive cerebellar ataxia with mental retardation (dysequilibrium syndrome).

Authors:  Kym M Boycott; Carsten Bonnemann; Joachim Herz; Stephanie Neuert; Chandree Beaulieu; James N Scott; Anuradha Venkatasubramanian; Jillian S Parboosingh
Journal:  J Child Neurol       Date:  2009-03-30       Impact factor: 1.987

7.  A missense founder mutation in VLDLR is associated with Dysequilibrium Syndrome without quadrupedal locomotion.

Authors:  Bassam R Ali; Jennifer L Silhavy; Matthew J Gleeson; Joseph G Gleeson; Lihadh Al-Gazali
Journal:  BMC Med Genet       Date:  2012-09-14       Impact factor: 2.103

Review 8.  Two 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.

Authors:  Uner Tan
Journal:  Front Neurosci       Date:  2014-04-22       Impact factor: 4.677

9.  Human quadrupeds, primate quadrupedalism, and Uner Tan Syndrome.

Authors:  Liza J Shapiro; Whitney G Cole; Jesse W Young; David A Raichlen; Scott R Robinson; Karen E Adolph
Journal:  PLoS One       Date:  2014-07-16       Impact factor: 3.240

10.  Human quadrupedalism is not an epiphenomenon caused by neurodevelopmental malformation and ataxia.

Authors:  Sibel Karaca; Meliha Tan; Uner Tan
Journal:  Front Neurol       Date:  2012-10-25       Impact factor: 4.003
  10 in total

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