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Uner Tan

Showing results (51-60 of 61) with videos related to

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The International Journal of Neuroscience|December 19, 2002
Blood brain barrier in right- and left-pawed female rats assessed by a new staining methodNecip Kutlu, H Seda Vatansever, T Onur Bayazit, et al.
The International Journal of Neuroscience|July 31, 2003
Differential contributions of right and left brains to paw skill in right- and left-pawed female ratsDerya Deniz Elalmis, Kerem Tuncay Ozgünen, Seçil Binokay, et al.
The International Journal of Neuroscience|February 27, 2008
"Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scansUner Tan, Sadrettin Pençe, Mustafa Yilmaz, et al.
The International Journal of Neuroscience|July 30, 2005
Effects of exercise on visual evoked potentialsRecep Ozmerdivenli, Serpil Bulut, Hale Bayar, et al.
The International Journal of Neuroscience|November 29, 2007
Unertan syndrome: a case series demonstrating human devolutionUner Tan, Sibel Karaca, Meliha Tan, et al.
The International Journal of Neuroscience|November 29, 2007
The effect of progesterone on total brain tissue sialic acid levels in experimental epilepsySadrettin Pence, Mehmet Bosnak, Naciye Kurtul, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotionOnur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
The International Journal of Neuroscience|December 19, 2002
Blood brain barrier in right- and left-pawed female rats assessed by a new staining methodNecip Kutlu, H Seda Vatansever, T Onur Bayazit, et al.
The International Journal of Neuroscience|July 31, 2003
Differential contributions of right and left brains to paw skill in right- and left-pawed female ratsDerya Deniz Elalmis, Kerem Tuncay Ozgünen, Seçil Binokay, et al.
The International Journal of Neuroscience|February 27, 2008
"Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scansUner Tan, Sadrettin Pençe, Mustafa Yilmaz, et al.
The International Journal of Neuroscience|July 30, 2005
Effects of exercise on visual evoked potentialsRecep Ozmerdivenli, Serpil Bulut, Hale Bayar, et al.
The International Journal of Neuroscience|November 29, 2007
Unertan syndrome: a case series demonstrating human devolutionUner Tan, Sibel Karaca, Meliha Tan, et al.
The International Journal of Neuroscience|November 29, 2007
The effect of progesterone on total brain tissue sialic acid levels in experimental epilepsySadrettin Pence, Mehmet Bosnak, Naciye Kurtul, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotionOnur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Pageof 7