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2012
Mark Characterization of mutations in barley fch2 encoding chlorophyllide a oxygenase
Mueller, A. H. ; Dockter, C. ; Gough, S. P. ; Lundqvist, U. ; von Wettstein, D. and Hansson, Mats ^LU (2012) In Plant and Cell Physiology 53(7). p.1232-1246
- Contribution to journal › Article
2007
Mark Transient erythromycin resistance phenotype associated with peptidyl-tRNA drop-off on early UGG and GGG codons
Macvanin, Mirjana ; Gonzalez de Valdivia, Ernesto I ^LU ; Ardell, David H and Isaksson, Leif A (2007) In Journal of Bacteriology 189(24). p.8993-9000
- Contribution to journal › Article
2005
Mark Size of the protein-coding genome and rate of molecular evolution
Rajic, Zoran A ; Jankovic, Gradimir M ; Vidovic, Ana ; Milic, Natasa M ; Skoric, Dejan ; Pavlovic, Milorad and Lazarevic, Vladimir ^LU (2005) In Journal of Human Genetics 50. p.29-217
- Contribution to journal › Article
Mark Abortive translation caused by peptidyl-tRNA drop-off at NGG codons in the early coding region of mRNA
Gonzalez de Valdivia, Ernesto I ^LU and Isaksson, Leif A (2005) In The FEBS Journal 272(20). p.16-5306
- Contribution to journal › Article
2004
Mark A codon window in mRNA downstream of the initiation codon where NGG codons give strongly reduced gene expression in Escherichia coli
Gonzalez de Valdivia, Ernesto I ^LU and Isaksson, Leif A (2004) In Nucleic Acids Research 32(17). p.205-5198
- Contribution to journal › Article
2003
Mark Functional split and crosslinking of the membrane domain of the beta subunit of proton-translocating transhydrogenase from Escherichia coli
Althage, Magnus ; Karlsson, Jenny ; Gourdon, Pontus ^LU ; Levin, Mikael ; Bill, Roslyn M ; Tigerström, Anna and Rydström, Jan (2003) In Biochemistry 42(37). p.10998-11003
- Contribution to journal › Article
2002
Mark Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.
Irshaid, Nidal M ; Eicher, Nicole I ; Hustinx, Hein ; Poole, Joyce and Olsson, Martin L ^LU (2002) In British Journal of Haematology 116(2). p.445-453
- Contribution to journal › Article
1997
Mark A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
Norlund, Lena ^LU ; Holm, Johan ^LU ; Zöller, Bengt ^LU and Öhlin, Ann-Kristin ^LU (1997) In Thrombosis and Haemostasis 77(2). p.51-248
- Contribution to journal › Article
1996
Mark Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
Mikkola, Hanna ; Yee, Vivien C. ; Syrjälä, Martti ; Seitz, Rainer ; Egbring, Rudolf ; Petrini, Pia ; Ljung, Rolf ^LU ; Ingerslev, Jorgen ; Teller, David C. and Palotie, Aarno ^LU (1996) In Blood 87(1). p.141-151
- Contribution to journal › Article
1990
Mark Two factor IX mutations in the family of an isolated haemophilia B patient : direct carrier diagnosis by amplification mismatch detection (AMD)
Montandon, A J ; Green, P M ; Bentley, D R ; Ljung, R ^LU ; Nilsson, Inga Marie and Giannelli, F (1990) In Human Genetics 85(2). p.4-200
- Contribution to journal › Article

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