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Late-Infantile Neuronal Ceroid Lipfuscinosis

Known as: Jansky Bielschowsky Disease, Disease, Jansky-Bielschowsky, NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE 
A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically… Expand
National Institutes of Health

Papers overview

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Review
2013
Review
2013
In childhood the neuronal ceroid lipofuscinoses (NCL) are the most frequent lysosomal diseases and the most frequent… Expand
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Highly Cited
2008
Highly Cited
2008
Late infantile neuronal ceroid lipofuscinosis (LINCL) is an autosomal recessive, neurodegenerative lysosomal storage disease… Expand
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Highly Cited
2008
Highly Cited
2008
Late infantile neuronal ceroid lipofuscinosis (LINCL) is an autosomal recessive neurodegenerative disease caused by mutations in… Expand
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Highly Cited
2007
Highly Cited
2007
The late-infantile-onset forms are the most genetically heterogeneous group among the autosomal recessively inherited… Expand
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Highly Cited
2002
Highly Cited
2002
The CLN6 gene that causes variant late-infantile neuronal ceroid lipofuscinosis (vLINCL), a recessively inherited… Expand
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Highly Cited
1998
Highly Cited
1998
The neuronal ceroid lipofuscinoses (NCLs) represent a group of common recessive inherited neurodegenerative disorders of… Expand
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Highly Cited
1997
Highly Cited
1997
Classical late-infantile neuronal ceroid lipofuscinosis (LINCL) is a fatal neurodegenerative disease whose defective gene has… Expand
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Highly Cited
1995
Highly Cited
1995
In budding yeast G1 cells increase in cell mass until they reach a critical cell size, at which point (called Start) they enter S… Expand
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Highly Cited
1993
Highly Cited
1993
In the budding yeast Saccharomyces cerevisiae, the G1 cyclins Cln1, Cln2 and Cln3 regulate entry into the cell cycle (Start) by… Expand
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Highly Cited
1990
Highly Cited
1990
The S. cerevisiae CLN genes encode cyclin homologs essential for progression from G1 to S phase. The CLN2 gene encodes a 62 kd… Expand
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