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3q26.1
A chromosome band present on 3q.
National Institutes of Health
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2 relations
Chromosomes
MIR15B wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature.
U. Dutta
,
I. Hansmann
,
D. Schlote
European Journal of Medical Genetics
2015
Corpus ID: 37748539
2013
2013
Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.
C. Jacob
,
H. Weber
,
+5 authors
A. Reif
Journal of Psychiatric Research
2013
Corpus ID: 34187485
2011
2011
Deletion polymorphism at chromosome 3q26.1 and oral squamous cell carcinoma
Homare Kawachi
,
K. Sugahara
,
Yasutaka Nakamura
,
A. Katakura
,
K. Minaguchi
,
T. Shibahara
International Journal of Oncology
2011
Corpus ID: 3007144
Several recent studies have investigated DNA instability in malignancies including deletions and duplications of part of the…
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2009
2009
A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.
E. Şimşek
,
Ş. Savaş-Erdeve
,
O. Sakamoto
,
T. Doganci
,
Y. Dallar
Turkish Journal of Pediatrics
2009
Corpus ID: 30633262
Fanconi-Bickel syndrome is a rare inherited disorder of carbohydrate metabolism. The disease is characterized by the association…
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2008
2008
Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens.
Chia-Huei Lee
,
Chien‐Chih Wu
,
Yi-No Wu
,
H. Chiang
Human Reproduction
2008
Corpus ID: 16380849
BACKGROUND Congenital bilateral absence of the vas deferens (CBAVD) is a distinct clinical entity accounting for approximately 25…
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2005
2005
Identification of a Novel Homozygous Deletion Region at 6q23.1 in Medulloblastomas Using High-Resolution Array Comparative Genomic Hybridization Analysis
A. Hui
,
H. Takano
,
+6 authors
H. Ng
Clinical Cancer Research
2005
Corpus ID: 15532374
Purpose: The aim of this study is to comprehensively characterize genome copy number aberrations in medulloblastomas using high…
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2004
2004
Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
S. Casas
,
A. Aventín
,
+12 authors
J. Sierra
Cancer Genetics and Cytogenetics
2004
Corpus ID: 41534383
Highly Cited
1998
Highly Cited
1998
Gain of 3q and deletion of 11q22 are frequent aberrations in mantle cell lymphoma
O. Monni
,
R. Oinonen
,
+4 authors
S. Knuutila
Genes, Chromosomes and Cancer
1998
Corpus ID: 28031195
We used comparative genomic hybridization (CGH) to screen for DNA copy number changes in 34 specimens from 27 cases of mantle…
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1996
1996
Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B.
D. Schultz
,
M. Litt
,
L. Smith
,
M. Thayer
,
K. McCormack
Genomics
1996
Corpus ID: 35219100
The gating properties and current amplitudes of mammalian voltage-activated Shaker potassium channels are modulated by at least…
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1995
1995
Chromosomal localization of the human ECT2 proto-oncogene to 3q26.1-->q26.2 by somatic cell analysis and fluorescence in situ hybridization.
S. Takai
,
J. Long
,
K. Yamada
,
T. Miki
Genomics
1995
Corpus ID: 37628804
The mouse ect2 oncogene was identified in a search of mitogenic signal transducers using a novel expression cloning strategy. In…
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