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Peptidylarginine deiminases (PADs) convert arginine residues in proteins into citrullines. They are suspected to be involved in… Expand The kinesin superfamily motor protein KIF1B has been shown to transport mitochondria. Here, we describe an isoform of KIF1B… Expand Atherogenic low density lipoproteins are cleared from the circulation by hepatic low density lipoprotein receptors (LDLR). Two… Expand Although the role of genetic factors in the origin of Parkinson disease has long been disputed, several genes involved in… Expand Classical congenital muscular dystrophies (CMDs) are autosomal recessive neuromuscular disorders characterized by early onset of… Expand Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in… Expand Previous reports on possible genomic imprinting of the neuroblastoma tumour suppressor gene on chromosome 1p36 have been… Expand Neuroblastoma is characterized by deletions of the short arm of chromosome 1 (1p) and amplification of the N-myc oncogene. We… Expand Mutations in the human APC gene caused various familial colon cancer syndromes. The Multiple intestinal neoplasia (Min) mouse… Expand Cytogenetic analyses of human colon cancer cells have revealed a high frequency of chromosome 1p deletions among other… Expand