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Larissa Arning

Showing results (1-10 of 95) with videos related to

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Molecular and Cellular Probes|July 16, 2016
The search for modifier genes in Huntington disease - Multifactorial aspects of a monogenic disorderLarissa Arning
Neurogenetics|June 12, 2013
Genetic modifiers in Huntington's disease: fiction or fact?Larissa Arning, Jörg T Epplen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Huntington disease update: new insights into the role of repeat instability in disease pathogenesisLarissa Arning, Huu Phuc Nguyen
Frontiers in Psychology|November 27, 2014
Handedness genetics: considering the phenotypeSebastian Ocklenburg, Christian Beste, Larissa Arning
Expert Review of Molecular Diagnostics|March 17, 2026
Challenges facing genetic diagnostics of Huntington's disease: an updateLarissa Arning, Carsten Saft, Huu Phuc Nguyen
Journal of Human Genetics|February 24, 2006
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European populationStefan Wieczorek, Larissa Arning, Ingrid Alheite, et al.
Neuropharmacology|November 9, 2010
The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processesChristian Beste, Daniel Schneider, Jörg T Epplen, et al.
European Journal of Medical Genetics|June 11, 2013
CNR1 variation is associated with the age at onset in Huntington diseaseEugen Kloster, Carsten Saft, Jörg T Epplen, et al.
Deutsche Medizinische Wochenschrift (1946)|July 17, 2020
[Targeted Early Detection and Prevention of Hereditary Colorectal Carcinomas]Klaus Zerres, Larissa Arning, Beatrix Böckmann, et al.
Neuroimage|August 27, 2014
On the relevance of the NPY2-receptor variation for modes of action cascading processesChristian Beste, Ann-Kathrin Stock, Jörg T Epplen, et al.
Pageof 10

Showing results (1-10 of 95) with videos related to

Sort By:
Pageof 10
Molecular and Cellular Probes|July 16, 2016
The search for modifier genes in Huntington disease - Multifactorial aspects of a monogenic disorderLarissa Arning
Neurogenetics|June 12, 2013
Genetic modifiers in Huntington's disease: fiction or fact?Larissa Arning, Jörg T Epplen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Huntington disease update: new insights into the role of repeat instability in disease pathogenesisLarissa Arning, Huu Phuc Nguyen
Frontiers in Psychology|November 27, 2014
Handedness genetics: considering the phenotypeSebastian Ocklenburg, Christian Beste, Larissa Arning
Expert Review of Molecular Diagnostics|March 17, 2026
Challenges facing genetic diagnostics of Huntington's disease: an updateLarissa Arning, Carsten Saft, Huu Phuc Nguyen
Journal of Human Genetics|February 24, 2006
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European populationStefan Wieczorek, Larissa Arning, Ingrid Alheite, et al.
Neuropharmacology|November 9, 2010
The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processesChristian Beste, Daniel Schneider, Jörg T Epplen, et al.
European Journal of Medical Genetics|June 11, 2013
CNR1 variation is associated with the age at onset in Huntington diseaseEugen Kloster, Carsten Saft, Jörg T Epplen, et al.
Deutsche Medizinische Wochenschrift (1946)|July 17, 2020
[Targeted Early Detection and Prevention of Hereditary Colorectal Carcinomas]Klaus Zerres, Larissa Arning, Beatrix Böckmann, et al.
Neuroimage|August 27, 2014
On the relevance of the NPY2-receptor variation for modes of action cascading processesChristian Beste, Ann-Kathrin Stock, Jörg T Epplen, et al.
Pageof 10