Use of chromosome substitution strains to identify seizure susceptibility loci in mice

By Winawer Melodie   Kuperman Rachel   Niethammer Martin   Sherman Steven   Rabinowitz Daniel   Guell Irene   Ponder Christine   Palmer Abraham  

Mammalian Genome, Vol. 18, Iss. 1, 2007-01 ,pp. : 23-31

Springer Publishing Company

Access to resources Recommend Favorite

Genetic and phenotypic analysis of seizure susceptibility in PL/J mice

By Kitami Toshimori  

Mammalian Genome, Vol. 15, Iss. 9, 2004-09 ,pp. : 698-703

Springer Publishing Company

Access to resources Recommend Favorite

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

By Gloeckner Christian Johannes   Kinkl Norbert   Schumacher Annette   Braun Ralf J.   O'Neill Eric   Meitinger Thomas   Kolch Walter   Prokisch Holger   Ueffing Marius  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 223-232

Oxford University Press

Access to resources Recommend Favorite

A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis

By Birve Anna   Neuwirth Christoph   Weber Markus   Marklund Stefan L.   Nilsson Ann-Charloth   Jonsson Per Andreas   Andersen Peter M.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4201-4206

Oxford University Press

Access to resources Recommend Favorite

Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin , a large novel gene

By Davy Brian E.   Robinson Michael L.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1163-1170

Oxford University Press

Access to resources Recommend Favorite