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B Wirth

Showing results (71-80 of 119) with videos related to

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European Journal of Human Genetics : EJHG|July 26, 2000
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA)C Helmken, A Wetter, S Rudnik-Schöneborn, et al.
Zeitschrift Fur Psychosomatische Medizin Und Psychoanalyse|January 1, 1989
[Psychoanalysis and psychotherapy management in Austria]E Jandl-Jager, G Stumm, B Wirth, et al.
Swiss Journal of Geosciences|April 25, 2022
Traces of a prehistoric and potentially tsunamigenic mass movement in the sediments of Lake Thun (Switzerland)Katrina Kremer, Stefano C Fabbri, Frederic M Evers, et al.
Human Genetics|March 2, 2006
Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy numberB Wirth, L Brichta, B Schrank, et al.
Human Molecular Genetics|February 22, 2001
Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophyS Jablonka, M Bandilla, S Wiese, et al.
American Journal of Human Genetics|November 1, 1996
Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generationsS Rudnik-Schöneborn, K Zerres, E Hahnen, et al.
Genomics|January 1, 1993
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studiesB Wirth, B Voosen, D Röhrig, et al.
Journal of Neuroscience Research|December 1, 1996
Regulation of connexin-43, GFAP, and FGF-2 is not accompanied by changes in astroglial coupling in MPTP-lesioned, FGF-2-treated parkinsonian miceM Rufer, S B Wirth, A Hofer, et al.
Stroke|June 1, 1995
Variability of vascular territory in stroke. Pitfalls and failure of stroke pattern interpretationE W Lang, M Daffertshofer, A Daffertshofer, et al.
Nucleic Acids Research|April 17, 2004
Differential evolution of the Saccharomyces cerevisiae DUP240 paralogs and implication of recombination in phylogenyV Leh-Louis, B Wirth, L Despons, et al.
Pageof 12

Showing results (71-80 of 119) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|July 26, 2000
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA)C Helmken, A Wetter, S Rudnik-Schöneborn, et al.
Zeitschrift Fur Psychosomatische Medizin Und Psychoanalyse|January 1, 1989
[Psychoanalysis and psychotherapy management in Austria]E Jandl-Jager, G Stumm, B Wirth, et al.
Swiss Journal of Geosciences|April 25, 2022
Traces of a prehistoric and potentially tsunamigenic mass movement in the sediments of Lake Thun (Switzerland)Katrina Kremer, Stefano C Fabbri, Frederic M Evers, et al.
Human Genetics|March 2, 2006
Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy numberB Wirth, L Brichta, B Schrank, et al.
Human Molecular Genetics|February 22, 2001
Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophyS Jablonka, M Bandilla, S Wiese, et al.
American Journal of Human Genetics|November 1, 1996
Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generationsS Rudnik-Schöneborn, K Zerres, E Hahnen, et al.
Genomics|January 1, 1993
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studiesB Wirth, B Voosen, D Röhrig, et al.
Journal of Neuroscience Research|December 1, 1996
Regulation of connexin-43, GFAP, and FGF-2 is not accompanied by changes in astroglial coupling in MPTP-lesioned, FGF-2-treated parkinsonian miceM Rufer, S B Wirth, A Hofer, et al.
Stroke|June 1, 1995
Variability of vascular territory in stroke. Pitfalls and failure of stroke pattern interpretationE W Lang, M Daffertshofer, A Daffertshofer, et al.
Nucleic Acids Research|April 17, 2004
Differential evolution of the Saccharomyces cerevisiae DUP240 paralogs and implication of recombination in phylogenyV Leh-Louis, B Wirth, L Despons, et al.
Pageof 12