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2013
Mark Rare allelic forms of PRDM9 associated with childhood leukemogenesis
Hussin, Julie ; Sinnett, Daniel ; Casals, Ferran ; Idaghdour, Youssef ; Bruat, Vanessa ; Saillour, Virginie ; Healy, Jasmine ; Grenier, Jean-Christophe ; de Malliard, Thibault and Busche, Stephan , et al. (2013) In Genome Research 23(3). p.30-419
- Contribution to journal › Article
Mark The pre-mRNA retention and splicing complex controls tRNA maturation by promoting TAN1 expression
Zhou, Yang ; Chen, Changchun and Johansson, Marcus J O ^LU (2013) In Nucleic Acids Research 41(11). p.78-5669
- Contribution to journal › Article
Mark Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Mezghani, Najla ; Ben Ayed, Imen and Fakhfakh, Faiza (2013) In Mitochondrial DNA 24(3). p.78-163
- Contribution to journal › Article
Mark A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Kammoun, Thouraya ; Alila-Fersi, Olfa ; Aloulou, Hajer ; Hachicha, Mongia and Fakhfakh, Faiza (2013) In Biochemical and Biophysical Research Communications 430(2). p.91-585
- Contribution to journal › Article
Mark Recognition of mono-ADP-ribosylated ARTD10 substrates by ARTD8 macrodomains
Forst, Alexandra H ; Karlberg, Tobias ^LU ; Herzog, Nicolas ; Thorsell, Ann-Gerd ; Gross, Annika ; Feijs, Karla L H ; Verheugd, Patricia ; Kursula, Petri ; Nijmeijer, Bianca and Kremmer, Elisabeth , et al. (2013) In Structure 21(3). p.75-462
- Contribution to journal › Article
2012
Mark Asexuals, Polyploids, Evolutionary Opportunists ...: The Population Genetics of Positive but Deteriorating Mutations.
Bengtsson, Bengt Olle ^LU (2012) In Genetics 191(4). p.499-1393
- Contribution to journal › Article
Mark The challenge of NSCLC diagnosis and predictive analysis on small samples. Practical approach of a working group
Thunnissen, Erik ; Kerr, Keith M. ; Herth, Felix J. F. ; Lantuejoul, Sylvie ; Papotti, Mauro ; Rintoul, Robert C. ; Rossi, Giulio ; Skov, Birgit G. ; Weynand, Birgit and Bubendorf, Lukas , et al. (2012) In Lung Cancer 76(1). p.1-18
- Contribution to journal › Scientific review
Mark Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin
Ohlsson, Monica ; Hedberg, Carola ; Brådvik, Björn ^LU ; Lindberg, Christopher ; Tajsharghi, Homa ; Danielsson, Olof ; Melberg, Atle ; Udd, Bjarne ; Martinsson, Tommy and Oldfors, Anders (2012) In Brain 135(6). p.1682-1694
- Contribution to journal › Article
Mark Origin of Swedish hemophilia A mutations
Halldén, C. ; Nilsson, D. ; Säll, Torbjörn ^LU ; Lind-Hallden, C. ; Liden, A. C. and Ljung, Rolf ^LU (2012) In Journal of Thrombosis and Haemostasis 10(12). p.2503-2511
- Contribution to journal › Article
Mark Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events Implications for Mutation-Specific Response to beta-Blocker Therapy in Type 1 Long-QT Syndrome
Barsheshet, Alon ; Goldenberg, Ilan ; O-Uchi, Jin ; Moss, Arthur J. ; Jons, Christian ; Shimizu, Wataru ; Wilde, Arthur A. ; McNitt, Scott ; Peterson, Derick R. and Zareba, Wojciech , et al. (2012) In Circulation 125(16). p.1988-1988
- Contribution to journal › Article

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