AbstractMutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infantile NCL (INCL, MIM#256730). PPT1 removes long fatty acid chains such as palmitate from modified cysteine residues of proteins. The data shown here result from isolated protein complexes from PPT1-expressing SH-SY5Y stable cells that were subjected to single step affinity purification coupled to mass spectrometry (AP-MS). Prior to the MS analysis, we utilised a modified filter-aided sample preparation (FASP) protocol. Based on label free quantitative analysis of the data by SAINT, 23 PPT1 interacting partners (IP) were identified. A dense connectivity in PPT1 network was further revealed by functional coupling and extended network ana...
CLN1 disease (OMIM # 256730) is an early childhood ceroid-lipofuscinosis associated with mutated CLN...
CLN1 disease is a fatal inherited neurodegenerative lysosomal storage disease of early childhood, ca...
CLN1 disease (OMIM #256730) is an early childhood ceroid-lipofuscinosis associated with mutatedCLN1,...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
AbstractMutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cau...
ABSTRACT: Neuronal ceroid lipofuscinoses (NCL) are a group of inherited progressive childhood disord...
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 Background Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of r...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Neuronal ceroid lipofuscinoses (NCL) are the most commonly inherited progressive encephalopathies of...
Neuronal ceroid lipofuscinoses (NCL) are the most common inherited progressive encephalopathies of c...
Infantile neuronal ceroid lipofuscinosis (INCL) is a severe neurodegenerative disease caused by defi...
CLN1 disease (OMIM # 256730) is an early childhood ceroid-lipofuscinosis associated with mutated CLN...
CLN1 disease is a fatal inherited neurodegenerative lysosomal storage disease of early childhood, ca...
CLN1 disease (OMIM #256730) is an early childhood ceroid-lipofuscinosis associated with mutatedCLN1,...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
Mutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cause Infan...
AbstractMutations in the CLN1 gene that encodes Palmitoyl protein thioesterase 1 (PPT1) or CLN1, cau...
ABSTRACT: Neuronal ceroid lipofuscinoses (NCL) are a group of inherited progressive childhood disord...
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 Background Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of r...
Palmitoyl-protein thioesterase 1 (PPT1) is a depalmitoylation enzyme that is mutated in cases of neu...
Neuronal ceroid lipofuscinoses (NCL) are the most commonly inherited progressive encephalopathies of...
Neuronal ceroid lipofuscinoses (NCL) are the most common inherited progressive encephalopathies of c...
Infantile neuronal ceroid lipofuscinosis (INCL) is a severe neurodegenerative disease caused by defi...
CLN1 disease (OMIM # 256730) is an early childhood ceroid-lipofuscinosis associated with mutated CLN...
CLN1 disease is a fatal inherited neurodegenerative lysosomal storage disease of early childhood, ca...
CLN1 disease (OMIM #256730) is an early childhood ceroid-lipofuscinosis associated with mutatedCLN1,...