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Neuroreport
|
October 16, 2009
Adult neural precursor cells unaffected in animal models of DYT1 dystonia
Martin Regensburger, Zacharias Kohl, Kathrin Grundmann, et al.
Breast Cancer Research and Treatment
|
November 27, 2009
High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays
Christopher Schroeder, Fanny Stutzmann, Bernhard H F Weber, et al.
Brain Research
|
September 17, 2002
Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease
Nils Rahner, Carsten Holzmann, Rejko Krüger, et al.
Plos One
|
January 4, 2017
The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory
Erik Karl Håkan Clemensson, Laura Emily Clemensson, Olaf Riess, et al.
Journal of Neurochemistry
|
July 22, 2005
Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation
Andreas Bauer, Karl Zilles, Andreas Matusch, et al.
BMC Medical Genetics
|
June 23, 2012
Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients
Yu-Chun Tsai, Silke Metzger, Olaf Riess, et al.
Psychoneuroendocrinology
|
November 9, 2007
Association between genetic variants of IL-1beta, IL-6 and TNF-alpha cytokines and cognitive performance in the elderly general population of the MEMO-study
Bernhard T Baune, Gerald Ponath, Matthias Rothermundt, et al.
Neuroscience Letters
|
February 3, 2007
Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease
Nadine Abahuni, Suzana Gispert, Peter Bauer, et al.
Personalized Medicine
|
January 5, 2022
Patient views on genetics and functional imaging for precision medicine: a willingness-to-pay analysis
Kerstin Clasen, Cihan Gani, Christopher Schroeder, et al.
Plos One
|
April 30, 2013
Cerebellar soluble mutant ataxin-3 level decreases during disease progression in Spinocerebellar Ataxia Type 3 mice
Huu Phuc Nguyen, Jeannette Hübener, Jonasz Jeremiasz Weber, et al.
Page
of 32
Search research articles
Search
Showing results (21-30 of 313) with videos related to
Sort By:
Page
of 32
Neuroreport
|
October 16, 2009
Adult neural precursor cells unaffected in animal models of DYT1 dystonia
Martin Regensburger, Zacharias Kohl, Kathrin Grundmann, et al.
Breast Cancer Research and Treatment
|
November 27, 2009
High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays
Christopher Schroeder, Fanny Stutzmann, Bernhard H F Weber, et al.
Brain Research
|
September 17, 2002
Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease
Nils Rahner, Carsten Holzmann, Rejko Krüger, et al.
Plos One
|
January 4, 2017
The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory
Erik Karl Håkan Clemensson, Laura Emily Clemensson, Olaf Riess, et al.
Journal of Neurochemistry
|
July 22, 2005
Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation
Andreas Bauer, Karl Zilles, Andreas Matusch, et al.
BMC Medical Genetics
|
June 23, 2012
Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients
Yu-Chun Tsai, Silke Metzger, Olaf Riess, et al.
Psychoneuroendocrinology
|
November 9, 2007
Association between genetic variants of IL-1beta, IL-6 and TNF-alpha cytokines and cognitive performance in the elderly general population of the MEMO-study
Bernhard T Baune, Gerald Ponath, Matthias Rothermundt, et al.
Neuroscience Letters
|
February 3, 2007
Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease
Nadine Abahuni, Suzana Gispert, Peter Bauer, et al.
Personalized Medicine
|
January 5, 2022
Patient views on genetics and functional imaging for precision medicine: a willingness-to-pay analysis
Kerstin Clasen, Cihan Gani, Christopher Schroeder, et al.
Plos One
|
April 30, 2013
Cerebellar soluble mutant ataxin-3 level decreases during disease progression in Spinocerebellar Ataxia Type 3 mice
Huu Phuc Nguyen, Jeannette Hübener, Jonasz Jeremiasz Weber, et al.
Page
of 32