Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Malgorzata J, Pytlos"'
Publikováno v:
BioTechniques, Vol 38, Iss 2, Pp 247-253 (2005)
The generation of long uninterrupted DNA repeats is important for the study of repeat instability associated with several human genetic diseases, including myotonic dystrophy type 1. However, obtaining defined lengths of long repeats in vitro has bee
Externí odkaz:
https://doaj.org/article/510e05d9f9b341afa9d30f275fd786d3
Publikováno v:
PLoS Biology, Vol 4, Iss 11, p e350 (2006)
Antigen receptor gene rearrangements are initiated by the RAG1/2 protein complex, which recognizes specific DNA sequences termed RSS (recombination signal sequences). The RAG recombinase can also catalyze transposition: integration of a DNA segment b
Externí odkaz:
https://doaj.org/article/87ec591b421d4bb49c6ed7c84d3b31a3
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 595:5-22
(CTG)n.(CAG)n repeats undergo deletion at a high rate in plasmids in Escherichia coli in a process that involves RecA and RecB. In addition, DNA replication fork progression can be blocked during synthesis of (CTG)n.(CAG)n repeats. Replication forks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6596de17e6be6bc125ed73e9c8c2d8f6
https://doi.org/10.1016/j.mrfmmm.2005.07.010
https://doi.org/10.1016/j.mrfmmm.2005.07.010
Publikováno v:
Frontiers in bioscience : a journal and virtual library. 12
Slipped strand DNA structures are formed when complementary strands comprising direct repeats pair in a misaligned, or slipped, fashion along the DNA helix axis. Although slipped strand DNA may form in almost any direct repeat, to date, these structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c938b2b0e409a6dc4b8c37c35c3f4d1d
https://pubmed.ncbi.nlm.nih.gov/17569609
https://pubmed.ncbi.nlm.nih.gov/17569609
Publikováno v:
Nucleic Acids and Molecular Biology ISBN: 9783540333357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::723b1de310d5d62afbe57f6f04b4cb3e
https://doi.org/10.1007/3-540-33336-3_1
https://doi.org/10.1007/3-540-33336-3_1
Publikováno v:
PLoS Biology
PLoS Biology, Vol 4, Iss 11, p e350 (2006)
PLoS Biology, Vol 4, Iss 11, p e350 (2006)
Antigen receptor gene rearrangements are initiated by the RAG1/2 protein complex, which recognizes specific DNA sequences termed RSS (recombination signal sequences). The RAG recombinase can also catalyze transposition: integration of a DNA segment b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9499165494d528eca5aa52a9f26de53
http://europepmc.org/articles/PMC1618415
http://europepmc.org/articles/PMC1618415
Publikováno v:
The Journal of biological chemistry. 281(38)
(CAG)(n)*(CTG)(n) expansion is associated with many neurodegenerative diseases. Repeat instability has been extensively studied in bacterial plasmids, where repeats undergo deletion at high rates. We report an assay for (CAG)(n)*(CTG)(n) deletion fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88c09ed89ad32d1cd5c0db4680396158
https://pubmed.ncbi.nlm.nih.gov/16873366
https://pubmed.ncbi.nlm.nih.gov/16873366
Autor:
Vera Hashem, Vladimir N. Potaman, Richard R. Sinden, Malgorzata J. Pytlos, Michael Leffak, John J. Bissler
This chapter discusses DNA structure and genetic instabilities associated with on spinocerebellar ataxia type 10 (ATTCT) n ·(AGAAT) n repeats. SCA10 is associated with expansion from a normal range of 10 to 22 10 (ATTCT) n ·(AGAAT) n pentanucleotid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5229a799fefeb2b4c109e0d88a517e5
https://doi.org/10.1016/b978-012369462-1/50031-4
https://doi.org/10.1016/b978-012369462-1/50031-4
Autor:
Aida Abu-Baker, Tetsuo Ashizawa, Linda L. Bachinski, Albino Bacolla, Gillian P. Bates, John S. Belt, Dya Bezprozvanny, Sanjay Bidichandani, John J. Bissler, Alexis Brice, Kerri M. Carlson, CheunJu Chen, Thomas A. Cooper, Natividad Cortez-Apreza, John W. Day, Irene De Biase, Ruhee Dere, Didier Devys, Katherine A. Dick, Vincent Dion, Lisa M. Ellerby, Henry F. Epstein, Kenneth H. Fischbeck, Laurent Foiry, Rune R. Frants, Gwenn A. Garden, M´rio Gomes-Pereira, Geneviéve Gourdon, Paul J. Hagerman, Randi J Hagerman, Peter S. Harper, Vera I. Hashem, Michael R. Hayden, Micheal L. Hebert, Dominique Helmlinger, Emma Hockly, Susan E. Holmes, H.S. Hwang, Yoshio Ikeda, Kinya Ishikawa, George R. Jackson, Mariana Kekis, Beata Kosmider, Irina V. Kovtun, Ralf Krahe, Wlodzimierz J. Krzyzosiak, Albert R. La Spada, Jacquelynn E. Larson, Rachel Lau, Michael Leffak, Michelle R. Leonard, Yunfu Lin, Yuan Liu, Julien L. Marcadier, Jamie M. Margolis, Russell L. Margolis, Cynthia T. McMurray, Sergei M. Mirkin, Hidehiro Mizusawa, Darren G. Monckton, S. Erin Montgomery, Marek Napierala, David L. Nelson, Elizabeth O'Hearn, Ben A. Oostra, Harry T. Orr, George W. Padberg, Massimo Pandolfo, Gagan B. Panigrahi, Sharan Paul, Henry Paulson, Christopher E. Pearson, Olga Pletnikova, Vladimir N. Potaman, Mahmoud A. Pouladi, Rajendra Prasad, Héléne Puccio, Stefan M. Pulst, Malgorzata J. Pytlos, Laura P.W. Ranum, Lynn A. Raymond, Sita Reddy, Robert I. Richards, Christopher A. Ross, Guy Rouleau, Dobrila D. Rudnicki, Tzu-Kang Sang, Peggy E. Shelbourne, Michael J. Siciliano, Richard R. Sinden, Ram Singh, Krzysztof Sobczak, LesHe S. Son, Giovanni Stevanin, S. Strack, Maurice S. Swanson, J. Paul Taylor, Charles A. Thornton, Andrea Todd, Juan Troncoso, Ray Truant, Bjarne Udd, Karen Usdin, Silvere M. van der Maarel, Rene E.M.A. van Herpen, Caroline Vosch, Derick G. Wansink, Robert D. Wells, Ronald Wetzel, Bé Wieringa, Robert B. Wilson, Samuel H. Wilson, John H. Wilson, Marzena Wojciechowska
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd4cd0ded2f3ce9679528ecf02b5ccd4
https://doi.org/10.1016/b978-012369462-1/50000-4
https://doi.org/10.1016/b978-012369462-1/50000-4
Autor:
Vera I, Hashem, Malgorzata J, Pytlos, Elzbieta A, Klysik, Kuniko, Tsuji, Mehrdad, Khajavi, Merhdad, Khajav, Tetsuo, Ashizawa, Richard R, Sinden
Publikováno v:
Nucleic Acids Research. 32:6717-6717
Myotonic dystrophy type 1 (DM1) is caused by the expansion of a (CTG)·(CAG) repeat in the DMPK gene on chromosome 19q13.3. At least 17 neurological diseases have similar genetic mutations, the expansion of DNA repeats. In most of these disorders, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af55c6eaef84a198c51b07c3e9eddccd
https://doi.org/10.1093/nar/gki147
https://doi.org/10.1093/nar/gki147