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1p31
A chromosome band present on 1p
National Institutes of Health
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Related topics
Related topics
9 relations
Chromosome 1 Short Arm
Chromosomes
DIRAS3 wt Allele
DNAJB4 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype.
M. Dizier
,
P. Margaritte-Jeannin
,
+10 authors
F. Demenais
Journal of Allergy and Clinical Immunology
2014
Corpus ID: 13951229
Review
2011
Review
2011
Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature
Marilena Petti
,
J. Samanich
,
+5 authors
M. Babcock
American Journal of Medical Genetics. Part A
2011
Corpus ID: 8606521
We report on the clinical and array‐based characterization of an interstitial 1p31.3 deletion in a 15‐year‐old male patient with…
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Review
2002
Review
2002
Cytogenetic Analysis in Mantle Cell Lymphoma: A Review of 214 Cases
W. Au
,
R. Gascoyne
,
D. Viswanatha
,
J. Connors
,
R. Klasa
,
D. Horsman
Leukemia and Lymphoma
2002
Corpus ID: 38057258
Cytogenetic (CG) analysis was performed in 78 consecutive cases of mantle cell lymphoma (MCL) at the British Columbia Cancer…
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2000
2000
Molecular and cytogenetic analysis of glioblastoma multiforme.
X. Mao
,
R. Hamoudi
Cancer Genetics and Cytogenetics
2000
Corpus ID: 11537821
Highly Cited
2000
Highly Cited
2000
ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers
Hongqi Peng
,
Feng-ji Xu
,
+7 authors
Yin-hua Yu
International Journal of Cancer
2000
Corpus ID: 24569112
In our previous work, we had characterized ARHI as an imprinted putative tumor‐suppressor gene in ovarian and breast cancers…
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2000
2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.
M. Vollmer
,
N. Jeck
,
+11 authors
N. Knoers
Nephrology, Dialysis and Transplantation
2000
Corpus ID: 36004235
BACKGROUND Recently a locus for antenatal Bartter syndrome associated with sensorineural deafness was mapped to human chromosome…
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1999
1999
TTC4, a novel human gene containing the tetratricopeptide repeat and mapping to the region of chromosome 1p31 that is frequently deleted in sporadic breast cancer.
G. Su
,
T. Roberts
,
J. Cowell
Genomics
1999
Corpus ID: 6360290
The 1p31 region shows loss of heterozygosity in up to 50% of human breast cancers, indicating the presence of a tumor suppressor…
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1990
1990
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic.
J. Kidd
,
Y. Matsubara
,
C. Castiglione
,
K. Tanaka
,
K. Kidd
Genomics
1990
Corpus ID: 2310215
1987
1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines.
T. Yang-Feng
,
D. Barton
,
L. Thelander
,
W. H. Lewis
,
P. R. Srinivasan
,
U. Francke
Genomics
1987
Corpus ID: 11820325
1984
1984
Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X).
A. Daniel
,
L. Ekblom
,
S. Phillips
American journal of medical genetics
1984
Corpus ID: 20405695
Fragile(X) estimations in fragile(X)-mental retardation hemizygotes or heterozygotes can become falsely negative in stored blood…
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