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pro vyhledávání: '"Katherine D. Amodeo"'
Autor:
Julia S. Schlehe, Marion S.M. Journel, Kelsey P. Taylor, Katherine D. Amodeo, Matthew J. LaVoie
Publikováno v:
Neurobiology of Disease, Vol 58, Iss , Pp 57-67 (2013)
Deficiency in human mitochondrial Complex-1 has been linked to a wide variety of neurological disorders. Homozygous deletion of the Complex-1 associated protein, Ndufaf2, leads to a severe juvenile onset encephalopathy involving degeneration of the s
Externí odkaz:
https://doaj.org/article/08232aace68a41aca1fc67dfb2785f8d
Autor:
Katherine D. Amodeo, Matthew J. LaVoie, Kelsey P. Taylor, Julia S. Schlehe, Marion S.M. Journel
Publikováno v:
Neurobiology of Disease, Vol 58, Iss, Pp 57-67 (2013)
Deficiency in human mitochondrial Complex-1 has been linked to a wide variety of neurological disorders. Homozygous deletion of the Complex-1 associated protein, Ndufaf2, leads to a severe juvenile onset encephalopathy involving degeneration of the s
Publikováno v:
Enzyme and Microbial Technology. 43:149-156
The biomass-processing enzymes laccase and xylanase can each be used to moderately reduce the amount of chlorine dioxide required for bleached pulp production. Although combined enzyme treatment is anticipated to be appealing to biomass-converting in
Autor:
Andreas Weihofen, Alison K. Berger, Giuseppe P. Cortese, Katherine D. Amodeo, Anthony Letai, Matthew J. LaVoie
Publikováno v:
Human molecular genetics. 18(22)
Autosomal-recessive mutations in the Parkin gene are the second most common cause of familial Parkinson's disease (PD). Parkin deficiency leads to the premature demise of the catecholaminergic neurons of the ventral midbrain in familial PD. Thus, a b