A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects

By Johnstone Karen A.   DuBose Amanda J.   Futtner Christopher R.   Elmore Michael D.   Brannan Camilynn I.   Resnick James L.  

Human Molecular Genetics, Vol. 15, Iss. 3, 2006-02 ,pp. : 393-404

Oxford University Press

Access to resources Recommend Favorite

Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel maturation

By Downes Meredith   Franois Mathias   Ferguson Charles   Parton Robert G.   Koopman Peter  

Human Molecular Genetics, Vol. 18, Iss. 15, 2009-08 ,pp. : 2839-2850

Oxford University Press

Access to resources Recommend Favorite

Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model

By Innis Jeffrey W.  

Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2841-2851

Oxford University Press

Access to resources Recommend Favorite

Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

By Khelfaoui Malik   Pavlowsky Alice   Powell Andrew D.   Valnegri Pamela   Cheong Kenneth W.   Blandin Yann   Passafaro Maria   Jefferys John G.R.   Chelly Jamel   Billuart Pierre  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2575-2583

Oxford University Press

Access to resources Recommend Favorite

Mitochondrial dysfunction and tau hyperphosphorylation in Ts1Cje, a mouse model for Down syndrome

By Shukkur Ebrahim Abdul   Shimohata Atsushi   Akagi Takumi   Yu Wenxin   Yamaguchi Mika   Murayama Miyuki   Chui Dehua   Takeuchi Tamaki   Amano Kenji   Subramhanya Karthik Harve   Hashikawa Tsutomu   Sago Haruhiko   Epstein Charles J.   Takashima Akihiko   Yamakawa Kazuhiro  

Human Molecular Genetics, Vol. 15, Iss. 18, 2006-09 ,pp. : 2752-2762

Oxford University Press

Access to resources Recommend Favorite