Search Results - "Lauridsen, Jes B."

Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice by Didriksen, Michael, PhD, Fejgin, Kim, PhD, Birknow, Michelle R., MSc, Larsen, Peter H., PhD, Lauridsen, Jes B., PhD, Nielsen, Vibeke, BSc, Kallunki, Pekka, PhD, Christensen, Kenneth V., PhD, Stensbøl, Tine B., PhD, Egebjerg, Jan, PhD, Nielsen, Jacob, PhD, Nilsson, Simon R.O., PhD, Grayton, Hannah M., PhD, Gastambide, Francois, PhD, Celada, Pau, PhD, Artigas, Francesc, PhD, Santana, Noemi, PhD, Werge, Thomas M., PhD, Bastlund, Jesper F., PhD

“…Background The hemizygous 22q11.2 microdeletion is a common copy number variant in humans. The deletion confers high risk for neurodevelopmental disorders,…”
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A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmission by Nielsen, Jacob, Fejgin, Kim, Sotty, Florence, Nielsen, Vibeke, Mørk, Arne, Christoffersen, Claus T., Yavich, Leonid, Lauridsen, Jes B., Clausen, Dorte, Larsen, Peter H., Egebjerg, Jan, Werge, Thomas M., Kallunki, Pekka, Christensen, Kenneth V., Didriksen, Michael

“…1q21.1 hemizygous microdeletion is a copy number variant leading to eightfold increased risk of schizophrenia. In order to investigate biological alterations…”
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The neural cell adhesion molecule binds to fibroblast growth factor receptor 2 by Christensen, Claus, Lauridsen, Jes B., Berezin, Vladimir, Bock, Elisabeth, Kiselyov, Vladislav V.

“…The neural cell adhesion molecule (NCAM) can bind to and activate fibroblast growth factor receptor 1 (FGFR1). However, there are four major FGFR isoforms…”
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A Mouse Model that Recapitulates Cardinal Features of the 15q13.3 Microdeletion Syndrome Including Schizophrenia- and Epilepsy-Related Alterations by Fejgin, Kim, Nielsen, Jacob, Birknow, Michelle R, Bastlund, Jesper F, Nielsen, Vibeke, Lauridsen, Jes B, Stefansson, Hreinn, Steinberg, Stacy, Sorensen, Helge B.D, Mortensen, Troels E, Larsen, Peter H, Klewe, Ib V, Rasmussen, Søren V, Stefansson, Kari, Werge, Thomas M, Kallunki, Pekka, Christensen, Kenneth V, Didriksen, Michael

“…Background Genome-wide scans have uncovered rare copy number variants conferring high risk of psychiatric disorders. The 15q13.3 microdeletion is associated…”
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