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1q23.2
A chromosome band present on 1q
National Institutes of Health
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Related topics
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2 relations
Chromosomes
chromosome 1q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
SUMO1P3 is associated clinical progression and facilitates cell migration and invasion through regulating miR-136 in non-small cell lung cancer.
Youwei Zhang
,
Yang Li
,
Liang Han
,
Peiying Zhang
,
Sanyuan Sun
Biomedicine & pharmacotherapy = Biomedecine…
2019
Corpus ID: 73498205
Highly Cited
2013
Highly Cited
2013
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Shuang-Xia Zhao
,
Li-qiong Xue
,
+25 authors
Huai-Dong Song
Human Molecular Genetics
2013
Corpus ID: 1528882
Graves' disease (GD), characterized by autoantibodies targeting antigens specifically expressed in thyroid tissues causing…
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Highly Cited
2009
Highly Cited
2009
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10
U. Scholl
,
Murim Choi
,
+7 authors
R. Lifton
Proceedings of the National Academy of Sciences…
2009
Corpus ID: 97925
We describe members of 4 kindreds with a previously unrecognized syndrome characterized by seizures, sensorineural deafness…
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2008
2008
Genetic Variation in C-Reactive Protein (CRP) Gene May Be Associated with Risk of Systemic Lupus Erythematosus and CRP Concentrations
P. B. Shih
,
S. Manzi
,
+6 authors
M. I. Kamboh
Journal of Rheumatology
2008
Corpus ID: 22665348
Objective The gene coding for C-reactive protein (CRP) is located on chromosome 1q23.2, which falls within a linkage region…
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2008
2008
Molecular analyses and identification of promising candidate genes for loci on mouse chromosome 1 affecting alcohol physical dependence and associated withdrawal
D. Denmark
,
K. J. Buck
Genes, Brain and Behavior
2008
Corpus ID: 20553298
We recently mapped quantitative trait loci (QTLs) with large effects on predisposition to physical dependence and associated…
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Highly Cited
2007
Highly Cited
2007
High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia
A. Tyybäkinoja
,
J. Vilpo
,
Sakari Knuutila
Cytogenetic and Genome Research
2007
Corpus ID: 32928177
Although recurrent chromosomal alterations occur in chronic lymphocytic leukemia (CLL), relatively few affected tumor suppressors…
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Review
2005
Review
2005
Analysis of the planar cell polarity gene Vangl2 and its co‐expressed paralogue Vangl1 in neural tube defect patients
K. Doudney
,
G. Moore
,
+5 authors
R. Stevenson
American Journal of Medical Genetics. Part A
2005
Corpus ID: 37332307
To the Editor:Neural tube defects (NTD) are a heterogeneous group ofcongenitalmalformationsthataffectthebrainandspinalcord.The…
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2005
2005
Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23
M. Lin
,
D. Lee
,
+6 authors
S. Tsai
British Journal of Dermatology
2005
Corpus ID: 43634045
Background There is a high incidence of primary cutaneous amyloidosis (PCA) in South America, South‐east Asia and Taiwan. To…
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Highly Cited
2001
Highly Cited
2001
Phosphorylation of uridine and cytidine nucleoside analogs by two human uridine-cytidine kinases.
A. R. Van Rompay
,
A. Norda
,
K. Lindén
,
M. Johansson
,
A. Karlsson
Molecular Pharmacology
2001
Corpus ID: 9290273
Uridine-cytidine kinases (UCK) have important roles for the phosphorylation of nucleoside analogs that are being investigated for…
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Highly Cited
1997
Highly Cited
1997
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.
Ellis J. Neufeld
,
Hanna Mandel
,
+7 authors
N. Cohen
American Journal of Human Genetics
1997
Corpus ID: 38265855
Thiamine-responsive megaloblastic anemia, also known as "TRMA" or "Rogers syndrome," is an early-onset autosomal recessive…
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