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1p31.1
A chromosome band present on 1p.
National Institutes of Health
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Related topics
Related topics
4 relations
Chromosome 1 Short Arm
Chromosomes
FUBP1 wt Allele
IFI44 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer
Hua Yuan
,
Hongliang Liu
,
+20 authors
Q. Wei
Scientific Reports
2016
Corpus ID: 13956751
Lung cancer etiology is multifactorial, and growing evidence has indicated that long non-coding RNAs (lncRNAs) are important…
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2013
2013
Transmission disequilibrium analysis of 31 type 1 diabetes susceptibility loci in Finnish families.
A. Laine
,
Mikael Knip
,
J. Ilonen
,
J. Ilonen
Tissue Antigens
2013
Corpus ID: 39311851
Currently more than 50 type 1 diabetes (T1D) loci outside the human leukocyte antigen (HLA)-region have been established in large…
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Review
2008
Review
2008
Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay
G. Maegawa
,
N. Poplawski
,
+4 authors
I. Teshima
American Journal of Medical Genetics. Part A
2008
Corpus ID: 20709384
We report on a 6‐year‐old girl who presented at 6 months of age with seizures, delayed psychomotor development and mild facial…
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Highly Cited
2007
Highly Cited
2007
Gene copy number analysis in malignant pleural mesothelioma using oligonucleotide array CGH
P. Lindholm
,
K. Salmenkivi
,
+4 authors
S. Knuutila
Cytogenetic and Genome Research
2007
Corpus ID: 27633883
Conventional cytogenetic analyses and comparative genomic hybridization have revealed a complex and even chaotic nature of…
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2006
2006
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1
I. Santa
2006
Corpus ID: 87104787
We have updated the clinical description of a large Scottish pedigree, in which patients were affected by spastic paraplegia…
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2005
2005
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1‐1p21.1
A. Orlacchio
,
T. Kawarai
,
F. Gaudiello
,
P. S. St George-Hyslop
,
R. Floris
,
G. Bernardi
Annals of Neurology
2005
Corpus ID: 32615660
We have updated the clinical description of a large Scottish pedigree, in which patients were affected by spastic paraplegia…
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2000
2000
Genomic structure and expression profile of LPHH1, a 7TM gene variably expressed in breast cancer cell lines.
G. White
,
J. Varley
,
J. Heighway
Biochimica et Biophysica Acta
2000
Corpus ID: 6299113
1999
1999
Genomic structure, 5' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene.
R. Betz
,
J. Lagercrantz
,
D. Kedra
,
J. Dumanski
,
A. Nordenskjöld
Biochemical and Biophysical Research…
1999
Corpus ID: 2966153
This paper describes the genomic structure of the human Prostaglandin F receptor gene (FP) with its exon-intron borders and 5…
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1995
1995
Chromosomal localization of the human prostanoid receptor gene family.
Alessandra M.V. Duncan
,
Linda Anderson
,
Colin D. Funk
,
Mark Abramovitz
,
Mohammed Adam
Genomics
1995
Corpus ID: 39619893
1995
1995
Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer.
Nigel Hoggard
,
Yvonne Hey
,
+5 authors
Jennifer M. Varley
Genomics
1995
Corpus ID: 43004568
We have mapped a region of high loss of heterozygosity in breast cancer to a 2-cM interval between the loci D1S430 and D1S465 on…
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