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12q21
A chromosome band present on 12q
National Institutes of Health
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Related topics
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4 relations
12q
Chromosomes
NTS wt Allele
PAWR wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Characterization of the 12q amplicons in lipomatous soft tissue tumors by multiplex ligation-dependent probe amplification-based copy number analysis.
D. Creytens
,
J. V. van Gorp
,
E. Speel
,
L. Ferdinande
Anticancer Research
2015
Corpus ID: 27563346
BACKGROUND/AIM Well-differentiated liposarcoma (WDLPS) and de-differentiated liposarcoma (DDLPS) are characterized by amplified…
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2013
2013
Deletion of chromosome 12q21 affecting KCNC2 and ATXN7L3B in a family with neurodevelopmental delay and ataxia
S. Rajakulendran
,
J. Roberts
,
M. Koltzenburg
,
M. Hanna
,
H. Stewart
Journal of Neurology Neurosurgery & Psychiatry
2013
Corpus ID: 8574028
Objective To describe the clinical and genetic findings in a family affected by neurodevelopmental delay and cerebellar ataxia…
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2013
2013
Silencing of Atp2b1 increases blood pressure through vasoconstriction
Young-Bin Shin
,
J. Lim
,
+7 authors
B. Oh
Journal of Hypertension
2013
Corpus ID: 13950323
Background: Recent genome-wide association studies (GWASs) have identified 30 genetic loci that regulate blood pressure…
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2012
2012
Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment — a cross-sectional…
L. Athanasiu
,
A. Brown
,
+6 authors
S. Djurovic
Psychiatry Research
2012
Corpus ID: 7616794
2008
2008
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
G. Nürnberg
,
F. Jacobi
,
+5 authors
C. Pusch
International Journal of Molecular Medicine
2008
Corpus ID: 23098475
Myopia, or short-sightedness, is the most common form of vision disorder worldwide. Higher levels of myopia, usually defined as…
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Highly Cited
2005
Highly Cited
2005
Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue.
L. Karenko
,
S. Hahtola
,
+18 authors
A. Ranki
Cancer Research
2005
Corpus ID: 24201573
Multicolor fluorescent in situ hybridization (FISH) was used to identify acquired chromosomal aberrations in 12 patients with…
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2002
2002
The novel t(11;12;18)(q21;q13;q21) represents a variant translocation of the t(11;18)(q21;q21) associated with MALT-type lymphoma
Judith Dierlamm
,
E. Penas
,
+9 authors
Dieter K. Hossfeld
Leukemia
2002
Corpus ID: 13340152
The novel t(11;12;18)(q21;q13;q21) represents a variant translocation of the t(11;18)(q21;q21) associated with MALT-type lymphoma
Review
1999
Review
1999
Cataract mutations and lens development 1 Dedicated to Prof. Udo H. Ehling on the occasion of his 70th birthday. 1
J. Graw
Progress in retinal and eye research
1999
Corpus ID: 33366679
Highly Cited
1998
Highly Cited
1998
Genomic analysis of DUSP6, a dual specificity MAP kinase phosphatase, in pancreatic cancer
Toru Furukawa
,
T. Yatsuoka
,
+9 authors
Akira Horii
Cytogenetic and Genome Research
1998
Corpus ID: 46883904
DUSP6 (alias PYST1), one of the dual-specificity tyrosine phosphatases, is localized on 12q21, one of the regions of frequent…
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Highly Cited
1998
Highly Cited
1998
Identification of two common regions of allelic loss in chromosome arm 12q in human pancreatic cancer.
M. Kimura
,
T. Furukawa
,
+9 authors
A. Horii
Cancer Research
1998
Corpus ID: 10991619
Using the method of microsatellite analysis, we studied 40 tissues with pancreatic ductal adenocarcinoma and identified two…
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