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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
Highly Cited
2001
Highly Cited
2001
The kinesin superfamily motor protein KIF1B has been shown to transport mitochondria. Here, we describe an isoform of KIF1B… 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
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
Highly Cited
1998
Highly Cited
1998
Classical congenital muscular dystrophies (CMDs) are autosomal recessive neuromuscular disorders characterized by early onset of… Expand
Highly Cited
1996
Highly Cited
1996
Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in… Expand
Highly Cited
1995
Highly Cited
1995
Previous reports on possible genomic imprinting of the neuroblastoma tumour suppressor gene on chromosome 1p36 have been… Expand
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
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
Review
1990
Review
1990
Cytogenetic analyses of human colon cancer cells have revealed a high frequency of chromosome 1p deletions among other… Expand
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