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R Stucka

Showing results (21-30 of 37) with videos related to

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Neuromuscular Disorders : NMD|June 8, 2000
A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homologyR Stucka, A Abicht, I H Song, et al.
Nucleic Acids Research|July 11, 1988
Sequence of a cDNA clone encompassing the complete mature human prostate specific antigen (PSA) and an unspliced leader sequenceP Schulz, R Stucka, H Feldmann, et al.
Yeast (Chichester, England)|December 1, 1992
DIT101 (CSD2, CAL1), a cell cycle-regulated yeast gene required for synthesis of chitin in cell walls and chitosan in spore wallsM Pammer, P Briza, A Ellinger, et al.
Yeast (Chichester, England)|September 1, 1994
Identification of a set of yeast genes coding for a novel family of putative ATPases with high similarity to constituents of the 26S protease complexR Schnall, G Mannhaupt, R Stucka, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiencyR Horvath, H Lochmüller, R Stucka, et al.
Neuropediatrics|July 13, 2004
Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ geneJ S Müller, S Petrova, R Kiefer, et al.
European Journal of Biochemistry|June 26, 2001
Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscleC Thirion, R Stucka, B Mendel, et al.
Neuropediatrics|January 22, 2003
Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit geneN Barisic, C Schmidt, O P Sidorova, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Two families with autosomal dominant progressive external ophthalmoplegiaS Kiechl, R Horváth, P Luoma, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|June 8, 2000
A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homologyR Stucka, A Abicht, I H Song, et al.
Nucleic Acids Research|July 11, 1988
Sequence of a cDNA clone encompassing the complete mature human prostate specific antigen (PSA) and an unspliced leader sequenceP Schulz, R Stucka, H Feldmann, et al.
Yeast (Chichester, England)|December 1, 1992
DIT101 (CSD2, CAL1), a cell cycle-regulated yeast gene required for synthesis of chitin in cell walls and chitosan in spore wallsM Pammer, P Briza, A Ellinger, et al.
Yeast (Chichester, England)|September 1, 1994
Identification of a set of yeast genes coding for a novel family of putative ATPases with high similarity to constituents of the 26S protease complexR Schnall, G Mannhaupt, R Stucka, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiencyR Horvath, H Lochmüller, R Stucka, et al.
Neuropediatrics|July 13, 2004
Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ geneJ S Müller, S Petrova, R Kiefer, et al.
European Journal of Biochemistry|June 26, 2001
Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscleC Thirion, R Stucka, B Mendel, et al.
Neuropediatrics|January 22, 2003
Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit geneN Barisic, C Schmidt, O P Sidorova, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Two families with autosomal dominant progressive external ophthalmoplegiaS Kiechl, R Horváth, P Luoma, et al.
Pageof 4