Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Karin Hammarström"'
Publikováno v:
Journal of Molecular Biology. 179:157-169
Three loci, designated U2/4, U2/6 and U2/7, which contain sequences related to human U2 RNA, have been studied. The U2/6 locus contains a tandem array of bona fide U2 genes. U2/4 and U2/7, in contrast, contain pseudogenes whose sequences deviate sign
Autor:
Lars-Göran Öfverstedt, Stellan Hjertén, N. Balgobin, Jyoti Chattopadhyaya, Karin Hammarström, Ulf Pettersson
Publikováno v:
Biochimica et biophysica acta. 782(2)
The use of displacement electrophoresis (synonymous to isotachophoresis, steady-state stacking, and moving boundary electrophoresis) for recovery of DNA fragments from agarose and polyacrylamide gels is described. Complete recovery of DNA molecules r
Publikováno v:
Nucleic acids research. 17(7)
Autor:
Hans-Jürg Monstein, Lennart Philipson, Jan Zabielski, Karin Hammarström, Ulf Pettersson, Gunnar Westin
Publikováno v:
Journal of molecular biology. 167(2)
Three clones U1-1, U1-6, and U1-8 containing sequences related to human U1 RNA have been studied by sequence analysis. The results show that each of the three clones represents a distinct locus. The U1-6 locus is closely related to the HU1-1 locus, w
Publikováno v:
Genomics. 3(4)
A MspI polymorphism was detected in the β-glucocerebrosidase gene in 10 Swedish families affected by type III Gaucher's disease. The sizes of the polymorphic fragments were 1.70 and 1.75 kb and the disease was found to segregate with the 1.70-kb fra
Autor:
Christina Bark, Jan Zabielski, Karin Hammarström, Gunnar Westin, Ulf Pettersson, Hans-Jürg Monstein
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 81(12)
Genes for the human small nuclear RNA U2 are present within 6.2-kilobase-pair-long tandem repeats. The haploid human genome contains approximately 20 such repeats, organized in one or a few very large clusters.
Publikováno v:
Experimental cell research. 159(2)
The gene cluster for human U2 RNA has been mapped to chromosome 17q21 by in situ hybridization and hybridization analysis of DNA from mouse/human somatic cell hybrids.
Autor:
Gösta Holmgren, Karin Hammarström-Heeroma, P. Goonewardena, Niklas Dahl, Karl-Henrik Gustavson, G.J.B. van Ommen, Claes Wadelius, Ulf Pettersson
Publikováno v:
Human genetics. 82(3)
A new cloned DNA probe (U6.2), which recognizes polymorphisms near the locus for the fragile-X syndrome, was isolated. No recombinations were observed between the probe and the disease locus, although recombinations were observed with several other p