User:Vincent Eijsink - Revision history

Vincent Eijsink at 18:27, 15 January 2018

2018-01-15T18:27:03Z

Vincent Eijsink at 18:26, 15 January 2018

2018-01-15T18:26:53Z

Vincent Eijsink at 18:25, 15 January 2018

2018-01-15T18:25:58Z

Vincent Eijsink at 18:24, 15 January 2018

2018-01-15T18:24:14Z

Vincent Eijsink at 18:23, 15 January 2018

2018-01-15T18:23:35Z

Vincent Eijsink at 18:22, 15 January 2018

2018-01-15T18:22:58Z

Vincent Eijsink at 18:22, 15 January 2018

2018-01-15T18:22:41Z

Vincent Eijsink at 18:16, 15 January 2018

2018-01-15T18:16:23Z

Vincent Eijsink at 18:14, 15 January 2018

2018-01-15T18:14:53Z

Vincent Eijsink at 18:13, 15 January 2018

2018-01-15T18:13:37Z

@@ Line 1: / Line 1: @@
 [[File:Vincent_Bilde.jpg|200px|right]]
-Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014</cite> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite> test.
+Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014</cite> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
 References

@@ Line 25: / Line 25: @@
 #Loose2016 pmid=27643617
 #Bissaro2017 pmid=28846668
-#Kuusk2017 pmid=29138240
+#Kuusk2018 pmid=29138240
 </biblio>
 [[Category:Contributors|Eijsink, Vincent]]

@@ Line 1: / Line 1: @@
 [[File:Vincent_Bilde.jpg|200px|right]]
-Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014</cite> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
+Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014</cite> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite> test.
 References

@@ Line 1: / Line 1: @@
 [[File:Vincent_Bilde.jpg|200px|right]]
-Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
+Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014</cite> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
 References

@@ Line 1: / Line 1: @@
 [[File:Vincent_Bilde.jpg|200px|right]]
-Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Westereng2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
+Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10]) after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
 References

@@ Line 1: / Line 1: @@
 [[File:Vincent_Bilde.jpg|200px|right]]
-Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Forsberg2014</cite> and was the first to describe LPMO activity on soluble substrates <cite>Isaksen2014> and beta-glucan hemicelluloses <cite>Agger2014</cite>. Recent developments include studies of substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
+Vincent Eijsink obtained an MSc in Molecular Sciences (Biochemistry) from Wageningen University and completed his PhD at the Groningen Biomolecular Sciences and Biotechnology Institute under the supervision of Gerard Venema in 1991. During his Ph.D. studies, focusing on the engineering of protein stability, he was co-supervised by Herman Berendsen, Bauke Dijkstra and Gert Vriend and he had several short stays in the Bioinformatics group at EMBL. In 1993, he moved to what is now called the Norwegian University of Life Sciences (NMBU), in Ås, Norway, where he became a full professor of Biochemistry in 1997. Work on CAZymes started off with work on [http://www.cazy.org/GH18.html family 18 chitinases] in the late 1990s, resulting in several papers on the structure and function of these enzymes <cite>VanAalten2000 VanAalten2001</cite>. Current chitin-related work focuses on [http://www.cazy.org/GH18.html family 18 chitinases] <cite>Horn2006 Zakariassen2009 Vaaje-Kolstad2013 </cite> and family 19 chitinases <cite>Hoell2006</cite>, whereas the group has a growing interest and activity in chitin deacetylases ([http://www.cazy.org/CE4.html CE family 4]) <cite>Liu2017 Tuveng2017</cite>. Recent research includes CAZyme discovery <cite>Pope2012 Larsbrink2016 Tuvengb2017</cite>. The Eijsink group is probably best known for the discovery of lytic polysaccharide monooxygenases (LPMOs) in 2010 <cite>Vaaje-Kolstad2010</cite> ([http://www.cazy.org/AA10.html AA family 10])after originally having detected chitinase boosting activity of what we now know is a chitin-active family AA10 LPMO in 2005 <cite>Vaaje-Kolstad2005</cite>. The group demonstrated AA10 activity on cellulose <cite>Forsberg2011 Westereng2011 Forsberg2014</cite> and was the first to describe activity of AA9 LPMOs ([http://www.cazy.org/AA11.html AA family 11]) on soluble substrates <cite>Isaksen2014> and beta-glucan hemicelluloses <cite>Agger2014 Borisova2015</cite>. Recent developments include studies of both AA9 and AA10, addressing topics such as substrate-binding <cite>Courtade2016</cite>, LPMO activation <cite>Loose2016</cite>, and the involvement of hydrogen peroxide in LPMO action <cite>Bissaro2017 Kuusk2018</cite>.
 References
@@ Line 21: / Line 21: @@
 #Isaksen2014 pmid=24324265
 #Agger2014 pmid=24733907
 #Courtade2016 pmid=27152023
 #Loose2016 pmid=27643617

@@ Line 17: / Line 17: @@
 #Vaaje-Kolstad2010 pmid=20929773
 #Vaaje-Kolstad2005 pmid=15929981
-#Forsberg2011 pmid=2178815
+#Forsberg2011 pmid=21748815
 #Forsberg2014 pmid=24912171
 #Isaksen2014 pmid=24324265

@@ Line 15: / Line 15: @@
 #Larsbrink2016 pmid=27933102
 #Tuvengb2017 pmid=27169553
-#Vaaje-Kolstad2010 pmid=20929778
+#Vaaje-Kolstad2010 pmid=20929773
 #Vaaje-Kolstad2005 pmid=15929981
 #Forsberg2011 pmid=2178815