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Neurogenetics

Showing results (161-170 of 1,080) with videos related to

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Neurogenetics|October 27, 2011
Restriction of trophic factors and nutrients induces PARKIN expressionM Klinkenberg, S Gispert, J A Dominguez-Bautista, et al.
Neurogenetics|December 29, 2011
Comment on the article "Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri" by van den Munckhof et alTrine E Prescott, Miriam J Smith, D Gareth Evans
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
Neurogenetics|March 3, 2011
A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C diseaseDagmara Kabzińska, Axel Niemann, Hanna Drac, et al.
Neurogenetics|March 14, 2012
A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigreeEvelyn B Skehan, Manal M A Abdulrahim, Nollaig A Parfrey, et al.
Neurogenetics|June 18, 2011
Audiogenic seizure proneness requires the contribution of two susceptibility loci in miceM Catharine Jawahar, Carolina I Sari, Yvette M Wilson, et al.
Neurogenetics|October 18, 2016
Recurrent KIF2A mutations are responsible for classic lissencephalyMara Cavallin, Emilia K Bijlsma, Adrienne El Morjani, et al.
Neurogenetics|October 9, 2014
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolateMarialuisa Quadri, Xu Yang, Giovanni Cossu, et al.
Neurogenetics|September 19, 2014
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approachMagdalena Zimoń, Esra Battaloğlu, Yesim Parman, et al.
Neurogenetics|July 17, 2014
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathiesShelisa Tey, Azlina Ahmad-Annuar, Alexander P Drew, et al.
Pageof 108

Showing results (161-170 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|October 27, 2011
Restriction of trophic factors and nutrients induces PARKIN expressionM Klinkenberg, S Gispert, J A Dominguez-Bautista, et al.
Neurogenetics|December 29, 2011
Comment on the article "Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri" by van den Munckhof et alTrine E Prescott, Miriam J Smith, D Gareth Evans
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
Neurogenetics|March 3, 2011
A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C diseaseDagmara Kabzińska, Axel Niemann, Hanna Drac, et al.
Neurogenetics|March 14, 2012
A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigreeEvelyn B Skehan, Manal M A Abdulrahim, Nollaig A Parfrey, et al.
Neurogenetics|June 18, 2011
Audiogenic seizure proneness requires the contribution of two susceptibility loci in miceM Catharine Jawahar, Carolina I Sari, Yvette M Wilson, et al.
Neurogenetics|October 18, 2016
Recurrent KIF2A mutations are responsible for classic lissencephalyMara Cavallin, Emilia K Bijlsma, Adrienne El Morjani, et al.
Neurogenetics|October 9, 2014
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolateMarialuisa Quadri, Xu Yang, Giovanni Cossu, et al.
Neurogenetics|September 19, 2014
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approachMagdalena Zimoń, Esra Battaloğlu, Yesim Parman, et al.
Neurogenetics|July 17, 2014
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathiesShelisa Tey, Azlina Ahmad-Annuar, Alexander P Drew, et al.
Pageof 108