Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Julie M. Bork"'
Publikováno v:
Journal of Molecular Biology. 265:519-540
RecA protein filaments formed on circular (ssDNA) in the presence of ssDNA binding protein (SSB) are generally stable as long as ATP is regenerated. On linear ssDNA, stable RecA filaments are believed to be formed by nucleation at random sites on the
Autor:
Julie M. Bork, Lies H. Hoefsloot, Frans P.M. Cremers, Lisa M. Astuto, Ronald J.E. Pennings, Hannie Kremer, Patrick L. M. Huygen, Arjan P.M. de Brouwer, Peter Van Hauwe, August F. Deutman, Cor W. R. J. Cremers, Bellinda van den Helm, Marjolijn Roeters, William J. Kimberling
Publikováno v:
Human Genetics, 112, 2, pp. 156-63
Human Genetics, 112, 153-63
Human Genetics, 112, 156-63
Human Genetics, 112, 2, pp. 153-63
Human Genetics, 112, 153-63
Human Genetics, 112, 156-63
Human Genetics, 112, 2, pp. 153-63
Item does not contain fulltext We have ascertained a multi-generation family with apparent autosomal recessive non-syndromic childhood hearing loss (DFNB). Failure to demonstrate linkage in a genome-wide scan with 300 polymorphic markers has suggeste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b233cd3168fe6b6eb27670f0c590d8
https://hdl.handle.net/2066/120676
https://hdl.handle.net/2066/120676
Autor:
Julie M, Bork, Robert J, Morell, Shaheen, Khan, Sheikh, Riazuddin, Edward R, Wilcox, Thomas B, Friedman, Andrew J, Griffith
Publikováno v:
Advances in oto-rhino-laryngology. 61
Publikováno v:
The EMBO journal. 20(24)
The Escherichia coli RecF, RecO and RecR pro teins have previously been implicated in bacterial recombinational DNA repair at DNA gaps. The RecOR-facilitated binding of RecA protein to single-stranded DNA (ssDNA) that is bound by single-stranded DNA-
Autor:
Anil K. Lalwani, Susan Bellman, Melvin D. Schloss, Zahoor Ahmed, Richard J.H. Smith, Seth L. Ness, Arabandi Ramesh, Sheikh Riazuddin, Thomas B. Friedman, Robert C. Polomeno, Edward R. Wilcox, C. R. Srikumari Srisailpathy, Julie M. Bork, Saima Riazuddin, Vazken M. Der Kaloustian, Walter E. Nance, Graeme Wistow, Shaheen N. Khan, Linda M. Peters, Dilip Desmukh, Xue-Zhong Liu, Zubair M. Ahmed, Robert J. Morell, Andrew J. Griffith, S. L. Bernstein, Maria Bitner-Glindzicz, X. Cindy Li, Sigrid Wayne
Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22. Seven highly consanguineous f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b2acf26b9bb7e65139c9a2f9e49d2fd
https://europepmc.org/articles/PMC1234923/
https://europepmc.org/articles/PMC1234923/