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T Gasser

Showing results (191-200 of 316) with videos related to

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Neurology|April 11, 2001
A polymorphism in the intronic region of the IL-1alpha gene and the risk for Parkinson's diseaseR C Dodel, F Lohmüller, Y Du, et al.
Neurology|June 16, 2005
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopaF Asmus, V Horber, J Pohlenz, et al.
Clinical Chemistry|February 4, 1999
Rapid detection of a pentanucleotide deletion polymorphism in the human alpha2-macroglobulin geneR C Dodel, K R Bales, M R Farlow, et al.
Microbiology Resource Announcements|December 10, 2024
Closing the genome of <i>Teredinibacter turnerae</i> T7902 by long-read nanopore sequencingMark T Gasser, Annie Liu, Ron Flatau, et al.
Neurology|July 26, 2006
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneityK M Liebetanz, J Winkelmann, C Trenkwalder, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|January 1, 1997
[Kidney transplantation from living donors]P Vogelbach, A Schütz, I Binet, et al.
Gene Therapy|August 15, 2008
Prevention of interferon-stimulated gene expression using microRNA-designed hairpinsM Bauer, N Kinkl, A Meixner, et al.
European Journal of Pain (London, England)|March 31, 2012
Cerebral somatic pain modulation during autogenic training in fMRIR P Naglatzki, M Schlamann, T Gasser, et al.
Human Gene Therapy|August 17, 2000
Nonviral glial cell-derived neurotrophic factor gene transfer enhances survival of cultured dopaminergic neurons and improves their function after transplantation in a rat model of Parkinson's diseaseM Bauer, M Meyer, L Grimm, et al.
Stroke|March 10, 2001
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyG Iannucci, M Dichgans, M Rovaris, et al.
Pageof 32

Showing results (191-200 of 316) with videos related to

Sort By:
Pageof 32
Neurology|April 11, 2001
A polymorphism in the intronic region of the IL-1alpha gene and the risk for Parkinson's diseaseR C Dodel, F Lohmüller, Y Du, et al.
Neurology|June 16, 2005
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopaF Asmus, V Horber, J Pohlenz, et al.
Clinical Chemistry|February 4, 1999
Rapid detection of a pentanucleotide deletion polymorphism in the human alpha2-macroglobulin geneR C Dodel, K R Bales, M R Farlow, et al.
Microbiology Resource Announcements|December 10, 2024
Closing the genome of <i>Teredinibacter turnerae</i> T7902 by long-read nanopore sequencingMark T Gasser, Annie Liu, Ron Flatau, et al.
Neurology|July 26, 2006
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneityK M Liebetanz, J Winkelmann, C Trenkwalder, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress|January 1, 1997
[Kidney transplantation from living donors]P Vogelbach, A Schütz, I Binet, et al.
Gene Therapy|August 15, 2008
Prevention of interferon-stimulated gene expression using microRNA-designed hairpinsM Bauer, N Kinkl, A Meixner, et al.
European Journal of Pain (London, England)|March 31, 2012
Cerebral somatic pain modulation during autogenic training in fMRIR P Naglatzki, M Schlamann, T Gasser, et al.
Human Gene Therapy|August 17, 2000
Nonviral glial cell-derived neurotrophic factor gene transfer enhances survival of cultured dopaminergic neurons and improves their function after transplantation in a rat model of Parkinson's diseaseM Bauer, M Meyer, L Grimm, et al.
Stroke|March 10, 2001
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyG Iannucci, M Dichgans, M Rovaris, et al.
Pageof 32