Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Catherine, Ross-Inta"'
Autor:
Eleonora Napoli, Catherine Ross-Inta, Sarah Wong, Connie Hung, Yasuko Fujisawa, Danielle Sakaguchi, James Angelastro, Alicja Omanska-Klusek, Robert Schoenfeld, Cecilia Giulivi
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42504 (2012)
Etiology of aberrant social behavior consistently points to a strong polygenetic component involved in fundamental developmental pathways, with the potential of being enhanced by defects in bioenergetics. To this end, the occurrence of social deficit
Externí odkaz:
https://doaj.org/article/71c772efedd048fd82f068891ea8be5c
Autor:
James L. Graham, Connie Hung, Eleonora Napoli, Pascal Froment, Peter J. Havel, Catherine Ross-Inta, Kimber L. Stanhope, Amanda L. Flores-Torres, Cecilia R Giulivi
Publikováno v:
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (10), pp.11270-11283. ⟨10.1096/fj.201802714R⟩
FASEB J
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol 33, iss 10
FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (10), pp.11270-11283. ⟨10.1096/fj.201802714R⟩
FASEB J
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol 33, iss 10
International audience; Ileal interposition (IT) is a surgical procedure that increases the delivery of incompletely digested nutrients and biliary and pancreatic secretions to the distal intestinal mucosa. Here, we investigated the metabolic impact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce364794aa47bd1bd40683f02606665
https://hal.inrae.fr/hal-02622880
https://hal.inrae.fr/hal-02622880
Autor:
Andrew W. Bollen, Jessie M. Cameron, Danika L. Bannasch, Sarah Wong, Catherine Ross-Inta, Eleonora Napoli, Karen M. Vernau, Peter J Dickinson, Cecilia R Giulivi
Publikováno v:
Brain Pathology. 25:441-453
Alaskan Husky encephalopathy (AHE(1) ) is a fatal brain disease associated with a mutation in SLC19A3.1 (c.624insTTGC, c.625C>A). This gene encodes for a thiamine transporter 2 with a predominately (CNS) central nervous system distribution. Consideri
Autor:
Dorothy W. Gietzen, John B. Rudell, John A. Payne, Irène Baccelli, Catherine Ross-Inta, James W. Sharp
Publikováno v:
Journal of neurochemistry, vol 127, iss 4
The anterior piriform cortex (APC) is activated by, and is the brain area most sensitive to, essential (indispensable) amino acid (IAA) deficiency. The APC is required for the rapid (20 min) behavioral rejection of IAA deficient diets and increased f
Autor:
Cecilia R Giulivi, Connie Hung, Sarah Wong, Eleonora Napoli, Prithvi R. Bomdica, Catherine Ross-Inta
Publikováno v:
Human molecular genetics, vol 22, iss 5
Hum Mol Genet
Hum Mol Genet
A number of studies have been conducted that link mitochondrial dysfunction (MD) to Huntington's disease (HD); however, contradicting results had resulted in a lack of a clear mechanism that links expression of mutant Huntingtin protein and MD. Mouse
Autor:
Yonggang Li, Catherine Ross-Inta, Cecilia R Giulivi, Cuimei Liu, Gregory D. Ford, Teclemichael Tewolde, Byron D. Ford, Donald A. Bruun, Pamela J. Lein
Publikováno v:
Toxicology and Applied Pharmacology. 262:194-204
Current medical countermeasures against organophosphate (OP) nerve agents are effective in reducing mortality, but do not sufficiently protect the CNS from delayed brain damage and persistent neurological symptoms. In this study, we examined the effi
Autor:
Vicente C. Quintanilla, Cecilia R Giulivi, Donna F. Kusewitt, Jimi L. Brandon, Fernando Benavides, Jean Jaubert, Kirstin F. Barnhart, Irma B. Gimenez-Conti, Nancy W. Otto, Catherine Ross-Inta, John DiGiovanni, Claudio J. Conti, Carlos J. Perez, Jean-Louis Guénet, Isabelle Aubin
Publikováno v:
American Journal of Pathology
American Journal of Pathology, 2010, 177 (4), pp.1958-1968. ⟨10.2353/ajpath.2010.100118⟩
American Journal of Pathology, American Society for Investigative Pathology, 2010, 177 (4), pp.1958-1968. ⟨10.2353/ajpath.2010.100118⟩
American Journal of Pathology, 2010, 177 (4), pp.1958-1968. ⟨10.2353/ajpath.2010.100118⟩
American Journal of Pathology, American Society for Investigative Pathology, 2010, 177 (4), pp.1958-1968. ⟨10.2353/ajpath.2010.100118⟩
International audience; Citrullinemia type I (CTLN1, OMIM# 215700) is an inherited urea cycle disorder that is caused by an argininosuccinate synthetase (ASS) enzyme deficiency. In this report, we describe two spontaneous hypomorphic alleles of the m
Autor:
Cedrick Barrow, Catherine Ross-Inta, Randi J Hagerman, Alicja Omanska-Klusek, Sarah Wong, Paul J. Hagerman, Christine Iwahashi, Dolores Garcia-Arocena, Cecilia R Giulivi, Elizabeth Berry-Kravis
Publikováno v:
Biochemical Journal. 429:545-552
FXTAS (fragile X-associated tremor/ataxia syndrome) is a late-onset neurodegenerative disorder that affects individuals who are carriers of premutation expansions (55–200 CGG repeats) in the 5′ untranslated region of the FMR1 (fragile X mental re
Publikováno v:
American Journal of Physiology-Gastrointestinal and Liver Physiology. 296:G1130-G1139
Diets deficient in an indispensable amino acid are known to suppress food intake in rats. Few studies were focused at understanding how amino acid-deficient diets may elicit biochemical changes at the mitochondrial level. The goal of this study was t
Publikováno v:
Biochemical Journal. 415:309-316
No studies have been performed on the mitochondria of malaria vector mosquitoes. This information would be valuable in understanding mosquito aging and detoxification of insecticides, two parameters that have a significant impact on malaria parasite