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1p35

A chromosome band present on 1p
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
Peptidylarginine deiminases (PADs) convert arginine residues in proteins into citrullines. They are suspected to be involved in… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract The kinesin superfamily motor protein KIF1B has been shown to transport mitochondria. Here, we describe an isoform of… Expand
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Highly Cited
2001
Highly Cited
2001
Atherogenic low density lipoproteins are cleared from the circulation by hepatic low density lipoprotein receptors (LDLR). Two… Expand
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Highly Cited
2001
Highly Cited
2001
Although the role of genetic factors in the origin of Parkinson disease has long been disputed, several genes involved in… Expand
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2001
2001
A previous loss of heterozygosity (LOH) study of a series of 91 neuroblastomas suggested that the 1p35-36 region encodes at least… Expand
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1998
1998
Classical congenital muscular dystrophies (CMDs) are autosomal recessive neuromuscular disorders characterized by early onset of… Expand
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1996
1996
Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in… Expand
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Highly Cited
1995
Highly Cited
1995
Neuroblastoma is characterized by deletions of the short arm of chromosome 1 (1p) and amplification of the N-myc oncogene. We… Expand
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1995
1995
Previous reports on possible genomic imprinting of the neuroblastoma tumour suppressor gene on chromosome 1p36 have been… Expand
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Highly Cited
1993
Highly Cited
1993
Mutations in the human APC gene caused various familial colon cancer syndromes. The Multiple intestinal neoplasia (Min) mouse… Expand
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