Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Neeraja Sammeta"'
Autor:
Holly J Garringer, Jill Murrell, Neeraja Sammeta, Anita Gnezda, Bernardino Ghetti, Ruben Vidal
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56426 (2013)
Familial Danish dementia (FDD) is an autosomal dominant neurodegenerative disease caused by a 10-nucleotide duplication-insertion in the BRI(2) gene. FDD is clinically characterized by loss of vision, hearing impairment, cerebellar ataxia and dementi
Externí odkaz:
https://doaj.org/article/3658966c3ecb4825b920b442fba4ae7e
Publikováno v:
Neurobiology of Aging. 52:90-97
Familial British dementia (FBD) and familial Danish dementia (FDD) are caused by mutations in the BRI2 gene. These diseases are characterized clinically by progressive dementia and ataxia and neuropathologically by amyloid deposits and neurofibrillar
Autor:
Timothy S. McClintock, Neeraja Sammeta
Publikováno v:
The Journal of Comparative Neurology. 518:1825-1836
More than any other neuron, olfactory sensory neurons are exposed to environmental insults. Surprisingly, their only documented response to damaging stress is apoptosis and subsequent replacement by new neurons. However, they expressed unfolded prote
Autor:
Neeraja Sammeta, Timothy S. McClintock
Publikováno v:
NeuroReport. 14:1547-1552
Olfactory receptors lead lives of exclusivity and privilege, the monarchs of fiefdoms organized solely to carry out their instructions. Each olfactory sensory neuron expresses one allele of one of approximately 1000 olfactory receptor genes. It is th
Autor:
Anita Gnezda, Bernardino Ghetti, Holly J. Garringer, Ruben Vidal, Jill R. Murrell, Neeraja Sammeta
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 2, p e56426 (2013)
PLoS ONE, Vol 8, Iss 2, p e56426 (2013)
Familial Danish dementia (FDD) is an autosomal dominant neurodegenerative disease caused by a 10-nucleotide duplication-insertion in the BRI(2) gene. FDD is clinically characterized by loss of vision, hearing impairment, cerebellar ataxia and dementi
Autor:
Neeraja Sammeta, Ruben Vidal, Kumar Sambamurti, Holly Garringer, Bernardino Ghetti, Bruce T. Lamb, Leticia Miravalle
Publikováno v:
Alzheimer's & Dementia. 8
Autor:
Bruce T. Lamb, Kumar Sambamurti, Neeraja Sammeta, Bernardino Ghetti, Ruben Vidal, Holly J. Garringer, Leticia Miravalle
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 26(7)
Genetically engineered mice have been generated to model cerebral β-amyloidosis, one of the hallmarks of Alzheimer disease (AD) pathology, based on the overexpression of a mutated cDNA of the amyloid-β precursor protein (AβPP) or by knock-in of th
Publikováno v:
Molecular and cellular neurosciences. 45(4)
Uncx (Phd1, Chx4) is a paired homeobox transcription factor gene. It and its probable functional partners, Tle co-repressors, were expressed by neurally-fated basal progenitor cells and olfactory sensory neurons of the olfactory epithelium. Uncx expr
Autor:
Timothy S. McClintock, Neeraja Sammeta
Identification of the > 10 000 genes expressed by olfactory sensory neurons reveals the biological processes and pathways active in these neurons. Expression profiling for odorant receptors, the largest mammalian gene family, confirms their expressio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7de9a4787025916c03d613984ad17527
https://doi.org/10.1016/b978-008045046-9.00189-3
https://doi.org/10.1016/b978-008045046-9.00189-3
Publikováno v:
The Journal of comparative neurology. 502(6)
Olfactory epithelial cells from olfactory marker protein-green fluorescent protein (OMP-GFP) mice were separated by fluorescence-activated cell sorting into a GFP+ sample enriched in mature olfactory sensory neurons (OSNs) and a GFP– sample enriche