PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotype

Author： Okazawa H.  

Publisher： Oxford University Press

E-ISSN： 0964-6906|12|7|711-725

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.12, Iss.7, 2003-04, pp. : 711-725

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice

By Wong Margaret   Martin Lee J.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2284-2302

Oxford University Press

Access to resources Recommend Favorite

I-cell disease-like phenotype in mice deficient in mannose 6-phosphate receptors

By Dittmer F.  

Transgenic Research, Vol. 7, Iss. 6, 1998-01 ,pp. : 473-483

Springer Publishing Company

Access to resources Recommend Favorite

Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice

By Schilling Gabriele  

Human Molecular Genetics, Vol. 13, Iss. 15, 2004-08 ,pp. : 1599-1610

Oxford University Press

Access to resources Recommend Favorite

N88S seipin mutant transgenic mice develop features of seipinopathy/BSCL2-related motor neuron disease via endoplasmic reticulum stress

By Yagi Takuya   Ito Daisuke   Nihei Yoshihiro   Ishihara Tadayuki   Suzuki Norihiro  

Human Molecular Genetics, Vol. 20, Iss. 19, 2011-10 ,pp. : 3831-3840

Oxford University Press

Access to resources Recommend Favorite

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice

By Borchelt D.R.  

Human Molecular Genetics, Vol. 11, Iss. 6, 2002-03 ,pp. : 633-640

Oxford University Press

Access to resources Recommend Favorite