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1p32.3
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
PCSK9 wt Allele
ZFYVE9 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Clinical characteristics and prognostic values of 1p32.3 deletion detected through fluorescence in situ hybridization in patients with newly diagnosed multiple myeloma: a single-center study in China
Huanping Wang
,
H. Meng
,
+8 authors
Jie Jin
Frontiers in Medicine
2019
Corpus ID: 208338205
This study aimed to investigate the prevalence, clinical characteristics, and prognostic impact of 1p32.3 deletion in patients…
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2018
2018
Abstract 4233: Racial differences in patterns of cytogenetic abnormalities in multiple myeloma
M. Chernoff
,
M. Sukhanova
,
Liz Stepniak
,
Wei Zhang
,
B. Chiu
Epidemiology
2018
Corpus ID: 81386306
Introduction: African American (AA) patients with Multiple Myeloma (MM) are diagnosed at younger ages and show an age-adjusted…
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2013
2013
Abnormalities Of FAM46C, AHCYL1, CDC14A and CDKN2C Genes Located At Chromosome 1p Detected By QM-FISH Identifies Deletion Of 1p32.3 Covered CDKN2C Is An Independent Adverse Prognostic Marker In…
Li-ping Hu
,
F. Jin
,
+7 authors
L. Qiu
2013
Corpus ID: 73813870
SNP arrays and FISH showed Chromosome 1 appeared as a critical region in MM pathogenesis and was associated with adverse survival…
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2010
2010
Title : A compendium of myeloma associated chromosomal copy number abnormalities and their prognostic value Short Title : SNP-based genome mapping in myeloma
B. Walker
,
P. Leone
,
+16 authors
G. Morgan
2010
Corpus ID: 74298336
2009
2009
Gain of 1q21 Does Not Predict for Immediate Progression in MGUS.
L. Chiecchio
,
G. Dagrada
,
+6 authors
F. Ross
2009
Corpus ID: 208429263
Abstract 123 In 30% to 40% of multiple myeloma tumours there is a gain of sequences at 1q21. These gains are highly associated…
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2008
2008
Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning…
Gregory J. Fitzgibbon
,
J. Clayton-Smith
,
+6 authors
L. Gaunt
Journal of Medical Case Reports
2008
Corpus ID: 6376348
IntroductionMonosomy 1p36 is one of the most common terminal deletion syndromes, with an approximate incidence of 1 in every 5000…
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2007
2007
Detailed assessment of copy number alterations revealing homozygous deletions in 1p and 13q in mantle cell lymphoma.
E. Flordal Thelander
,
K. Ichimura
,
+7 authors
S. Lagercrantz
Leukemia research : a Forum for Studies on…
2007
Corpus ID: 21383608
2003
2003
Isolation and characterization of a novel human thioredoxin-like gene hTLP19 encoding a secretory protein.
Feng Liu
,
Y. Rong
,
Ling-Chun Zeng
,
Xin Zhang
,
Ze-Guang Han
Gene
2003
Corpus ID: 20166037
2003
2003
Analysis of 148 kb of Genomic DNA of Tetraodon nigroviridis Covering an Amylase Gene Family*
L. Bouneau
,
Guillaume Lardier
,
Cécile Fischer
,
Muriel Ronsin
,
J. Weissenbach
,
A. Bernot
DNA Sequence
2003
Corpus ID: 22610511
We have sequenced and analysed a 148 kb genomic region of Tetraodon nigroviridis, a teleost fish with a compact genome. Several…
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1998
1998
Identification and characterization of the gene encoding a second proteolipid subunit of human vacuolar H(+)-ATPase (ATP6F).
H. Nishigori
,
S. Yamada
,
+4 authors
J. Takeda
Genomics
1998
Corpus ID: 39946954
The proteolipid domain of vacuolar H(+)-ATPase (V-ATPase) plays a major role in H+ transport in microvesicles and other acidic…
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