Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neuronal ceroid lipofuscinosis (NCL). The hallmarks of the disease include progressive neurodegeneration and blindness, as well as seizures. In the current study, we identified 62 high-confident PPT1-binding proteins. These proteins included a self-interaction of PPT1, two V-type ATPases, calcium voltage-gated channels, cytoskeletal proteins and others. Pathway analysis suggested their involvement in seizures and neuronal morphology. We then proceeded to demonstrate that hippocampal neurons from Ppt1−/− mice exhibit structural deficits, and further investigated electrophysiology parameters in the hippocampi of mutant mice, both in brain slices a...
Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by the a...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
Infantile neuronal ceroid lipofuscinosis (INCL) is a severe neurodegenerative disease caused by defi...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
ABSTRACT: Neuronal ceroid lipofuscinoses (NCL) are a group of inherited progressive childhood disord...
Protein palmitoylation and depalmitoylation alter protein function. This post-translational modifica...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Abstract Background Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of r...
AbstractMutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cau...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Mutations in the depalmitoylating enzyme gene, PPT1, cause the infantile form of Neuronal Ceroid Lip...
The small GTPases from the Ras superfamily play crucial roles in basic cellular processes during pra...
<p><b>Copyright information:</b></p><p>Taken from "Glycosylation, transport, and complex formation o...
Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by the a...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
Infantile neuronal ceroid lipofuscinosis (INCL) is a severe neurodegenerative disease caused by defi...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
ABSTRACT: Neuronal ceroid lipofuscinoses (NCL) are a group of inherited progressive childhood disord...
Protein palmitoylation and depalmitoylation alter protein function. This post-translational modifica...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Abstract Background Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of r...
AbstractMutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cau...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Mutations in the depalmitoylating enzyme gene, PPT1, cause the infantile form of Neuronal Ceroid Lip...
The small GTPases from the Ras superfamily play crucial roles in basic cellular processes during pra...
<p><b>Copyright information:</b></p><p>Taken from "Glycosylation, transport, and complex formation o...
Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by the a...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
Infantile neuronal ceroid lipofuscinosis (INCL) is a severe neurodegenerative disease caused by defi...