Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia

By Melo Daniela  

Journal of Bioenergetics and Biomembranes, Vol. 43, Iss. 1, 2011-02 ,pp. : 39-46

Springer Publishing Company

Access to resources Recommend Favorite

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy

By Daehmlow S.   Erdmann J.   Knueppel T.   Gille C.   Froemmel C.   Hummel M.   Hetzer R.   Regitz-Zagrosek V.  

Biochemical and Biophysical Research Communications, Vol. 298, Iss. 1, 2002-10 ,pp. : 116-120

Elsevier

Access to resources Recommend Favorite

Novel ganglioside found in adenocarcinoma cells of Lewis-negative patients

By Shida Kyoko   Korekane Hiroaki   Misonou Yoshiko   Noura Shingo   Ohue Masayuki   Takahashi Hidenori   Ohigashi Hiroaki   Ishikawa Osamu   Miyamoto Yasuhide  

Glycobiology, Vol. 20, Iss. 12, 2010-12 ,pp. : 1594-1606

Oxford University Press

Access to resources Recommend Favorite

Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber’s hereditary optic neuropathy (LHON)

By Rezvani Zahra   Didari Elmira   Arastehkani Ahoura   Ghodsinejad Vadieh   Aryani Omid   Kamalidehghan Behnam   Houshmand Massoud  

Molecular Biology Reports, Vol. 40, Iss. 12, 2013-12 ,pp. : 6837-6841

Springer Publishing Company

Access to resources Recommend Favorite

Functional Analysis of Five Endothelin-B Receptor Mutations Found in Human Hirschsprung Disease Patients

By Abe Y.   Sakurai T.   Yamada T.   Nakamura T.   Yanagisawa M.   Goto K.  

Biochemical and Biophysical Research Communications, Vol. 275, Iss. 2, 2000-08 ,pp. : 524-531

Elsevier

Access to resources Recommend Favorite