Carnitine Transport Defect in Fibroblasts of Juvenile Visceral Steatosis (JVS) Mouse

By Kuwajima M.   Lu K.M.   Harashima H.   Ono A.   Sato I.   Mizuno A.   Murakami T.   Nakajima H.   Miyagawa J.I.   Namba M.   Hanafusa T.   Hayakawa J.I.   Matsuzawa Y.   Shima K.  

Biochemical and Biophysical Research Communications, Vol. 223, Iss. 2, 1996-06 ,pp. : 283-287

Elsevier

Access to resources Recommend Favorite

Relative suppression of the sodium-dependent Vitamin C transport in mouse versus human lens epithelial cells

By Obrenovich Mark   Fan Xingjun   Satake Makoto   Jarvis Simon   Reneker Lixing   Reddan John   Monnier Vincent  

Molecular and Cellular Biochemistry, Vol. 293, Iss. 1-2, 2006-12 ,pp. : 53-62

Springer Publishing Company

Access to resources Recommend Favorite

Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality

By Burwinkel B.   Kreuder J.   Schweitzer S.   Vorgerd M.   Gempel K.   Gerbitz K-D.   Kilimann M.W.  

Biochemical and Biophysical Research Communications, Vol. 261, Iss. 2, 1999-08 ,pp. : 484-487

Elsevier

Access to resources Recommend Favorite

A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant

By Gliddon B.  

Glycobiology, Vol. 11, Iss. 1, 2001-01 ,pp. : 99-103

Oxford University Press

Access to resources Recommend Favorite

Genetic and Physical Delineation of the Region of the Mouse Deafness Mutation shaker-2

By Wakabayashi Y.   Kikkawa Y.   Matsumoto Y.   Shinbo T.   Kosugi S.   Chou D.   Furuya M.   Jishage K.   Noda T.   Yonekawa H.   Kominami R.  

Biochemical and Biophysical Research Communications, Vol. 234, Iss. 1, 1997-05 ,pp. : 107-110

Elsevier

Access to resources Recommend Favorite