Title : Substantial narrowing of the Niemann-Pick C candidate interval by yeast artificial chromosome complementation.

Pub. Date : 1997 Jul 8

PMID : 9207099






4 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Niemann-Pick disease type C (NP-C) is an autosomal recessive lipidosis linked to chromosome 18q11-12, characterized by lysosomal accumulation of unesterified cholesterol and delayed induction of cholesterol-mediated homeostatic responses. Cholesterol NPC intracellular cholesterol transporter 1 Homo sapiens
2 Niemann-Pick disease type C (NP-C) is an autosomal recessive lipidosis linked to chromosome 18q11-12, characterized by lysosomal accumulation of unesterified cholesterol and delayed induction of cholesterol-mediated homeostatic responses. Cholesterol NPC intracellular cholesterol transporter 1 Homo sapiens
3 Niemann-Pick disease type C (NP-C) is an autosomal recessive lipidosis linked to chromosome 18q11-12, characterized by lysosomal accumulation of unesterified cholesterol and delayed induction of cholesterol-mediated homeostatic responses. Cholesterol NPC intracellular cholesterol transporter 1 Homo sapiens
4 Niemann-Pick disease type C (NP-C) is an autosomal recessive lipidosis linked to chromosome 18q11-12, characterized by lysosomal accumulation of unesterified cholesterol and delayed induction of cholesterol-mediated homeostatic responses. Cholesterol NPC intracellular cholesterol transporter 1 Homo sapiens