Zobrazeno 1 - 10
of 40
pro vyhledávání: '"W. Rommerskirch"'
Autor:
Christoph Peters, W Rommerskirch, Regina Pohlmann, K von Figura, H E Meyer, K Rupp, M Zühlsdorf, Bernhard Schmidt, M Vingron
Publikováno v:
Journal of Biological Chemistry. 265:3374-3381
A 2.2-kilobase cDNA clone for human arylsulfatase B (ASB) and several genomic clones were isolated and sequenced. The deduced amino acid sequence of 533 amino acids contains a 41-amino acid N-terminal signal peptide and a mature polypeptide of 492 am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89ef278f4f9836ad23bbef5aca774245
https://doi.org/10.1016/s0021-9258(19)39778-9
https://doi.org/10.1016/s0021-9258(19)39778-9
Autor:
S, Kreusch, M, Fehn, G, Maubach, K, Nissler, W, Rommerskirch, K, Schilling, E, Weber, I, Wenz, B, Wiederanders
Publikováno v:
European journal of biochemistry. 267(10)
Cathepsin L-like cysteine proteinases contain an evolutionarily highly conserved alpha-helical motif in the proregion. This is called the ER(F/W)N(I/V)N motif according to the conserved amino acids along one side of the helix. We studied the function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::333a35280952a605901e1e1555122c29
https://pubmed.ncbi.nlm.nih.gov/10806395
https://pubmed.ncbi.nlm.nih.gov/10806395
Autor:
W Rommerskirch, K von Figura
Multiple sulfatase deficiency (MSD) is an inherited lysosomal storage disease characterized by the deficiency of at least seven sulfatases. The basic defect in MSD is thought to be in a post-translational modification common to all sulfatases. In acc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842ec88899e84a8f6171301c496d4603
https://europepmc.org/articles/PMC48701/
https://europepmc.org/articles/PMC48701/
Publikováno v:
The Biochemical journal. 280
Metachromatic leukodystrophy is a lysosomal storage disease caused by the deficiency of arylsulphatase A (ASA). A human ASA cDNA was subcloned into the retroviral vector pXT1. Replication-defective retrovirus was generated by transfection of the vect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d04f3f9e8b64b980dd89dd91f84e0af8
https://pubmed.ncbi.nlm.nih.gov/1684103
https://pubmed.ncbi.nlm.nih.gov/1684103
The Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI; MPS VI) is a lysosomal storage disease caused by deficiency of the enzyme arylsulphatase B (ASB). A human ASB cDNA has been subcloned into the retroviral vector pXT1 containing the bacterial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3583c093aad1361e55abcf8565ba4066
https://europepmc.org/articles/PMC1151119/
https://europepmc.org/articles/PMC1151119/
Autor:
C, Peters, B, Schmidt, W, Rommerskirch, K, Rupp, M, Zühlsdorf, M, Vingron, H E, Meyer, R, Pohlmann, K, von Figura
Publikováno v:
The Journal of biological chemistry. 265(6)
A 2.2-kilobase cDNA clone for human arylsulfatase B (ASB) and several genomic clones were isolated and sequenced. The deduced amino acid sequence of 533 amino acids contains a 41-amino acid N-terminal signal peptide and a mature polypeptide of 492 am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2355fadc2e143c8190612a22e140419e
https://pubmed.ncbi.nlm.nih.gov/2303452
https://pubmed.ncbi.nlm.nih.gov/2303452
Publikováno v:
Nucleic Acids Research. 16:941-952
Homologous recombination between microinjected SV40 DNA fragments and endogenous SV40 DNA in COS7 cells was analysed by immunofluorescence staining and DNA blotting. Time course experiments revealed that recombination between the transferred (trans)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08fd37590a808e66cb2fa9c919a3f2e6
https://doi.org/10.1093/nar/16.3.941
https://doi.org/10.1093/nar/16.3.941
Autor:
Stefan K. Bohlander, M. Fraccaro, Gerd Scherer, Gaby Müller, W. Rommerskirch, Werner Schempp, Ulrich Wolf
Publikováno v:
Human Genetics. 81:144-148
By in situ hybridization, Y-specific DNA sequences were localized on Xp22.3-Xpter of one of the two X chromosomes in all of eleven XX males studied. In nine of the cases the presence of the Y-specific DNA did not affect random X inactivation in fibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::357ba4a9c69fcd55fa5c5aa5b6ac8801
https://doi.org/10.1007/bf00293890
https://doi.org/10.1007/bf00293890
Autor:
G. Henzold, H. Trumpold, W. Lotze, P. Bauer, F. Goubeaud, U. Löffelhardt, W. Dutschke, W. Rommerskirch, M. Stäck, A. Weckenmann, E. Zehender
Publikováno v:
Fertigungsmeßtechnik ISBN: 9783642517532
Die Anforderungen an die funktionellen Merkmale geometrisch definierter Korper, einschlieslich Austauschbarkeit (s. Abschn. 4.1.9), verlangen vielfach, Abweichungen der Mase, der Form und der Lage von der vorgegebenen Geometrie innerhalb festgelegter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e1261e025d63884c2dfb367392e398
https://doi.org/10.1007/978-3-642-51752-5_4
https://doi.org/10.1007/978-3-642-51752-5_4
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