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Neurogenetics

Showing results (111-120 of 1,080) with videos related to

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Neurogenetics|June 17, 2006
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N geneYuji Okamoto, Hiroshi Takashima, Itsuro Higuchi, et al.
Neurogenetics|June 20, 2008
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosisL Blázquez, M Azpitarte, A Sáenz, et al.
Neurogenetics|March 30, 2004
Mutations of the MTHFR gene (428C>T and [458G>T+459C>T]) markedly decrease MTHFR enzyme activityHidetaka Yano, Kazuhiro Nakaso, Kenichi Yasui, et al.
Neurogenetics|August 9, 2005
The Gem interacting protein (GMIP) gene is associated with major depressive disorderKazuyuki Tadokoro, Ryota Hashimoto, Masahiko Tatsumi, et al.
Neurogenetics|January 17, 2004
Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breedsPetra Sander, Henning Hamann, Ina Pfeiffer, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Neurogenetics|September 30, 2004
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer diseaseKristin K Nicodemus, Judith E Stenger, Donald E Schmechel, et al.
Neurogenetics|December 4, 2003
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian familiesNacim Louhichi, Chahnez Triki, Susana Quijano-Roy, et al.
Neurogenetics|August 8, 2008
The location of DCX mutations predicts malformation severity in X-linked lissencephalyPierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, et al.
Neurogenetics|September 24, 2008
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)Thilo Herzfeld, Nicole Wolf, Pia Winter, et al.
Pageof 108

Showing results (111-120 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|June 17, 2006
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N geneYuji Okamoto, Hiroshi Takashima, Itsuro Higuchi, et al.
Neurogenetics|June 20, 2008
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosisL Blázquez, M Azpitarte, A Sáenz, et al.
Neurogenetics|March 30, 2004
Mutations of the MTHFR gene (428C>T and [458G>T+459C>T]) markedly decrease MTHFR enzyme activityHidetaka Yano, Kazuhiro Nakaso, Kenichi Yasui, et al.
Neurogenetics|August 9, 2005
The Gem interacting protein (GMIP) gene is associated with major depressive disorderKazuyuki Tadokoro, Ryota Hashimoto, Masahiko Tatsumi, et al.
Neurogenetics|January 17, 2004
Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breedsPetra Sander, Henning Hamann, Ina Pfeiffer, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Neurogenetics|September 30, 2004
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer diseaseKristin K Nicodemus, Judith E Stenger, Donald E Schmechel, et al.
Neurogenetics|December 4, 2003
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian familiesNacim Louhichi, Chahnez Triki, Susana Quijano-Roy, et al.
Neurogenetics|August 8, 2008
The location of DCX mutations predicts malformation severity in X-linked lissencephalyPierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, et al.
Neurogenetics|September 24, 2008
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)Thilo Herzfeld, Nicole Wolf, Pia Winter, et al.
Pageof 108