1p35

A chromosome band present on 1p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1988-2016
051019882016

Papers overview

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Highly Cited
2006
Highly Cited
2006
Neuroblastoma is remarkable for its clinical heterogeneity and is characterized by genomic alterations that are strongly… (More)
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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… (More)
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Highly Cited
2001
Highly Cited
2001
  • C M van Duijn, M C Dekker, +10 authors P Heutink
  • American journal of human genetics
  • 2001
Although the role of genetic factors in the origin of Parkinson disease has long been disputed, several genes involved in… (More)
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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… (More)
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2001
2001
Osteosarcomas (OS) are aggressive tumors of the bone and often have a poor prognosis. Conventional cytogenetic analyses of OS… (More)
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1997
1997
Phenotypic variability based on nonallelic heterogeneity is a characteristic feature of the dominantly inherited disease… (More)
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1996
1996
Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in… (More)
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1995
1995
Neuroblastoma is characterized by deletions of the short arm of chromosome 1 (1p) and amplification of the N-myc oncogene. We… (More)
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1995
1995
Previous reports on possible genomic imprinting of the neuroblastoma tumour suppressor gene on chromosome 1p36 have been… (More)
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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… (More)
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