Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alicja Omanska-Klusek"'
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:
Ana Alcaraz, Alicja Omanska-Klusek, Francisco A. Uzal, Jorge P. Garcia, Raul E. Marin, Robin Houston
Publikováno v:
Journal of Veterinary Diagnostic Investigation. 27:80-85
Tunga penetrans is the smallest biting flea known. In cattle, infestation by T. penetrans (tungiasis) typically affects the skin of the distal legs, udder, prepuce, and perianal area. A detailed clinical and pathologic description of bovine tungiasis
Publikováno v:
Journal of Virological Methods. 194:138-145
A single real-time multiplex quantitative PCR (qPCR) assay for the simultaneous detection of Grapevine virus A, B and D (GVA, GVB and GVD) was developed, using three different fluorescently labeled minor groove binding probes. This multiplex RT-qPCR
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
Autor:
Sarah Wong, Connie Hung, Danielle Sakaguchi, Yasuko Fujisawa, Robert Schoenfeld, James M. Angelastro, Cecilia R Giulivi, Alicja Omanska-Klusek, Catherine Ross-Inta, Eleonora Napoli
Publikováno v:
PloS one, vol 7, iss 8
PLoS ONE, Vol 7, Iss 8, p e42504 (2012)
PLoS ONE
PLoS ONE, Vol 7, Iss 8, p e42504 (2012)
PLoS ONE
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::353caea7ef581e5692674bb9e2cca373
https://escholarship.org/uc/item/03v7x3cx
https://escholarship.org/uc/item/03v7x3cx
Autor:
Alicja Omanska-Klusek, Eleonora Napoli, Dolores Garcia-Arocena, Cedrick Barrow, Christine Iwahashi, Catherine Ross-Inta, Paul J. Hagerman, Elizabeth Berry-Kravis, Randi J Hagerman, Danielle Sakaguchi, Cecilia R Giulivi, Sarah Wong
Publikováno v:
Human molecular genetics. 20(15)
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder that affects individuals who are carriers of small CGG premutation expansions in the fragile X mental retardation 1 (FMR1) gene. Mitochondrial dysfunction
Autor:
Isaac N. Pessah, Catherine Ross-Inta, Flora Tassone, Irva Hertz-Picciotto, Yi Fan Zhang, Sarah Wong, Alicja Omanska-Klusek, Cecilia R Giulivi
Publikováno v:
JAMA, vol 304, iss 21
Context Impaired mitochondrial function may influence processes highly dependent on energy, such as neurodevelopment, and contribute to autism. No studies have evaluated mitochondrial dysfunction and mitochondrial DNA (mtDNA) abnormalities in a well-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21cf1e73bee8302592184dbd17c494a
https://escholarship.org/uc/item/2hn2h17v
https://escholarship.org/uc/item/2hn2h17v
Autor:
Genaro C. Barrientos, Alicja Omanska-Klusek, Isaac N. Pessah, Paul D. Allen, Eleonora Napoli, Cecilia R Giulivi, Catherine Ross-Inta, Danielle Sakaguchi
Publikováno v:
The Journal of biological chemistry. 286(1)
Malignant hyperthermia (MH) and central core disease in humans have been associated with mutations in the skeletal ryanodine receptor (RyR1). Heterozygous mice expressing the human MH/central core disease RyR1 R163C mutation exhibit MH when exposed t
Autor:
Catherine Ross‑Inta, Alicja Omanska‑Klusek, Sarah Wong, Cedrick Barrow, Dolores Garcia‑Arocena, Christine Iwahashi, Elizabeth Berry‑Kravis, Cecilia Giulivi
Publikováno v:
Biochemical Journal; Jul2010, Vol. 429 Issue 3, p545-552, 8p