Search Results - "Oo, Tinmarla F."
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An early axonopathy in a hLRRK2(R1441G) transgenic model of Parkinson disease
Published in Neurobiology of disease (01-10-2015)“…Abstract Mutations in the gene for LRRK2 are the most common cause of familial Parkinson's disease (PD) and patients with these mutations manifest clinical…”
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2
Dopaminergic pathway reconstruction by Akt/Rheb-induced axon regeneration
Published in Annals of neurology (01-07-2011)“…Objective: A prevailing concept in neuroscience has been that the adult mammalian central nervous system is incapable of restorative axon regeneration. Recent…”
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3
Akt suppresses retrograde degeneration of dopaminergic axons by inhibition of macroautophagy
Published in The Journal of neuroscience (09-02-2011)“…Axon degeneration is a hallmark of neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease. Such degeneration is not a passive event…”
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4
Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain
Published in eLife (20-09-2016)“…The regulation of protein degradation is essential for maintaining the appropriate environment to coordinate complex cell signaling events and to promote…”
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5
Age and α-synuclein expression interact to reveal a dependence of dopaminergic axons on endogenous Akt/PKB signaling
Published in Neurobiology of disease (01-11-2011)“…Abstract The mechanisms underlying the chronic neurodegeneration that occurs in Parkinson's disease (PD) are unknown. One emerging hypothesis is that neural…”
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6
Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease
Published in Nature neuroscience (01-07-2009)“…Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson's disease. We created a LRRK2 transgenic mouse model that…”
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7
Brain-derived neurotrophic factor regulates early postnatal developmental cell death of dopamine neurons of the substantia nigra in vivo
Published in Molecular and cellular neuroscience (01-07-2009)“…Brain-derived neurotrophic factor (BDNF) was the first purified molecule identified to directly support the development of mesencephalic dopamine neurons…”
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8
Distinct Nuclear and Cytoplasmic Localization of Caspase Cleavage Products in Two Models of Induced Apoptotic Death in Dopamine Neurons of the Substantia Nigra
Published in Experimental neurology (01-05-2002)“…An emerging theme in programmed cell death (PCD) of neurons is that the mechanisms involved depend on the cellular context and the death-inducing stimulus. One…”
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JNK2 and JNK3 combined are essential for apoptosis in dopamine neurons of the substantia nigra, but are not required for axon degeneration
Published in Journal of neurochemistry (01-12-2008)“…Activation of c‐jun N‐terminal kinase (JNK) by the mitogen‐activated protein kinase cascade has been shown to play an important role in the death of dopamine…”
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10
Regulation of the postnatal development of dopamine neurons of the substantia nigra in vivo by Akt/protein kinase B
Published in Journal of neurochemistry (01-07-2009)“…Following mitosis, specification and migration during embryogenesis, dopamine neurons of the mesencephalon undergo a postnatal naturally occurring cell death…”
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11
Expression of cyclin‐dependent kinase 5 and its activator p35 in models of induced apoptotic death in neurons of the substantia nigra in vivo
Published in Journal of neurochemistry (01-06-2001)“…Cyclin‐dependent kinase 5 is predominantly expressed in postmitotic neurons and plays a role in neurite elongation during development. It has also been…”
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12
Mutant LRRK2R1441G BAC transgenic mice recapitulate cardinal features of Parkinson's disease
Published in Nature neuroscience (07-06-2009)“…Mutations in LRRK2 can cause Parkinson's disease. The authors create a transgenic mouse model of LRRK2 that recapitulates several cardinal features of the…”
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13
Increased Expression of Rat Synuclein in the Substantia Nigra Pars Compacta Identified by mRNA Differential Display in a Model of Developmental Target Injury
Published in Journal of neurochemistry (01-12-1999)“…: Human α‐synuclein was identified on the basis of proteolytic fragments derived from senile plaques of Alzheimer's disease, and it is the locus of mutations…”
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14
Activation of Caspase‐3 in Developmental Models of Programmed Cell Death in Neurons of the Substantia Nigra
Published in Journal of neurochemistry (01-07-1999)“…: Programmed cell death has been proposed to play a role in the death of neurons in acute and chronic degenerative neurologic disease. There is now evidence…”
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15
Upregulation of cytosolic branched chain aminotransferase in substantia nigra following developmental striatal target injury
Published in Brain research. Molecular brain research. (22-02-2000)“…We have previously shown that apoptotic cell death can be induced in substantia nigra (SN) by developmental striatal target lesion. In this model, only a…”
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16
Age and [alpha]-synuclein expression interact to reveal a dependence of dopaminergic axons on endogenous Akt/PKB signaling
Published in Neurobiology of disease (01-11-2011)“…The mechanisms underlying the chronic neurodegeneration that occurs in Parkinson's disease (PD) are unknown. One emerging hypothesis is that neural systems…”
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Journal Article -
17
Mutant LRRK2 super(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease
Published in Nature neuroscience (01-07-2009)“…Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson's disease. We created a LRRK2 transgenic mouse model that…”
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18
Mutant [LRRK2.sup.R1441G] BAC transgenic mice recapitulate cardinal features of Parkinson's disease
Published in Nature neuroscience (01-07-2009)“…Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson's disease. We created a LRRK2 transgenic mouse model that…”
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19
Mutant LRRK2 R1441G BAC transgenic mice recapitulate cardinal features of Parkinson's disease
Published in Nature neuroscience (01-07-2009)“…Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson's disease. We created a LRRK2 transgenic mouse model that…”
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20
Expression of c-fos, c-jun, and c-jun N-terminal kinase (JNK) in a developmental model of induced apoptotic death in neurons of the substantia nigra
Published in Journal of neurochemistry (01-02-1999)“…The transcription factors c-fos and c-jun have been proposed to play a role in the initiation of programmed cell death in neurons. We have shown that…”
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