Zobrazeno 1 - 10
of 19
pro vyhledávání: '"H. G. Nothwang"'
Autor:
J, Schulze, L, Nolte, S, Lyutenski, N, Tinne, D, Heinemann, T, Ripken, M A, Willaredt, H G, Nothwang, T, Lenarz, A, Warnecke
Publikováno v:
HNO. 67(8)
In the field of hearing research a variety of imaging techniques are available to study molecular and cellular structures of the cochlea. Most of them are based on decalcifying, embedding, and cutting of the cochlea. By means of scanning laser optica
Autor:
I. Silva Pereira, F. Recillas Targa, E. Viegas-Péquignot, Faycal Bey, H. G. Nothwang, B. Dutrillaux, Klaus Scherrer, Olivier Coux
Publikováno v:
Molecular and General Genetics MGG. :193-205
Monoclonal antibodies demonstrated high conservation during evolution of a prosomal protein of M(r) 27,000 and differentiation--specific expression of the epitope. More than 90% of the reacting antigen was found as a p27K protein in the free messenge
Publikováno v:
Biochemical Journal. 287:733-739
Prosomes are ribonucleoprotein particles constituted by a variable set of about 20 proteins found associated with untranslated mRNA. In addition, they contain a small RNA, the presence of which has been an issue of controversy for a long time. The in
Publikováno v:
Nucleic Acids Research. 20:1959-1965
Two-dimensional gel electrophoresis of HeLa cell prosomal RNAs, 3'-end labeled by RNA ligase, revealed one prominent spot. Determination of a partial sequence at the 3'-end indicated full homology to the 18 nucleotides at the 3'-end of tRNA(Lys,3) fr
Autor:
A, Schröer, M P, Scheer, S, Zacharias, S, Schneider, H H, Ropers, H G, Nothwang, J, Chelly, B, Hamel, J P, Fryns, P, Shaw, C, Moraine
Publikováno v:
American journal of medical genetics. 95(4)
Autor:
J, Wirth, H G, Nothwang, S, van der Maarel, C, Menzel, G, Borck, I, Lopez-Pajares, K, Brøndum-Nielsen, N, Tommerup, M, Bugge, H H, Ropers, T, Haaf
Publikováno v:
Journal of medical genetics. 36(4)
Disease associated balanced chromosome rearrangements (DBCRs) have been instrumental in the isolation of many disease genes. To facilitate the molecular cytogenetic characterisation of DBCRs, we have generated a set of >1200 non-chimeric, cytogenetic
Autor:
F, Hildebrandt, B, Strahm, H G, Nothwang, N, Gretz, B, Schnieders, I, Singh-Sawhney, R, Kutt, M, Vollmer, M, Brandis
Publikováno v:
Kidney international. 51(1)
Familial juvenile nephronophthisis (NPH), an autosomal recessive cystic disease of the kidney, is the most common genetic cause of end-stage renal disease (ESRD) in the first two decades of life. A gene locus for nephronophthisis type 1 (NPH1) has be
Autor:
K. Scherrer, H -G. Nothwang, I. Silva Pereira, F. Bey, M. Olink-Coux, M. Huesca, O. Coux, C. Arcangeletti, C. Chezzi, J -F. Buri, M -F. Grossi de Sa, J. K. Pal, O. Akhayat, C. Martins de Sa
Publikováno v:
Molecular biology reports. 14(2-3)
Autor:
Annika C. Arnberg, Wilma Bergsma-Schutter, H. G. Nothwang, Olivier Coux, Peter A. Timmins, Claudine Cohen-Addad, Klaus Scherrer, Jörg Langowski
Publikováno v:
FEBS Letters. (1):49-55
Duck erythroblasts prosomes were analysed by small angle neutron scattering (SANS), dynamic light scattering and (cryo-)electron microscopy. A molecular weight of approximately 720,000 +/- 50,000, a radius of gyration of 64 +/- 2 A and a hydrodynamic
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