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3q27
A chromosome band present on 3q
National Institutes of Health
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Related topics
Related topics
8 relations
ABCC5 wt Allele
ADIPOQ wt Allele
AHSG wt Allele
BCL6 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Adiponectin I164T mutation is associated with the metabolic syndrome and coronary artery disease.
K. Ohashi
,
N. Ouchi
,
+19 authors
Y. Matsuzawa
Journal of the American College of Cardiology
2004
Corpus ID: 30476794
Highly Cited
2004
Highly Cited
2004
Cytogenetic alterations affecting BCL6 are predominantly found in follicular lymphomas grade 3B with a diffuse large B-cell component.
T. Katzenberger
,
G. Ott
,
T. Klein
,
J. Kalla
,
H. Müller-hermelink
,
M. Ott
American Journal of Pathology
2004
Corpus ID: 38265380
Highly Cited
2003
Highly Cited
2003
Cloning, physical mapping and expression analysis of the human 5-HT3 serotonin receptor-like genes HTR3C, HTR3D and HTR3E.
B. Niesler
,
B. Frank
,
J. Kapeller
,
G. Rappold
Gene
2003
Corpus ID: 31311479
Highly Cited
2002
Highly Cited
2002
Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population.
K. Hara
,
P. Boutin
,
+21 authors
T. Kadowaki
Diabetes
2002
Corpus ID: 29564191
An adipocyte-derived peptide, adiponectin (also known as GBP28), is decreased in subjects with type 2 diabetes. Recent genome…
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Highly Cited
2002
Highly Cited
2002
Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity: interaction with family history of type 2 diabetes.
M. Stumvoll
,
O. Tschritter
,
+5 authors
H. Häring
Diabetes
2002
Corpus ID: 15723899
The adipocyte-derived hormone adiponectin seems to protect from insulin resistance, a key factor in the pathogenesis of type 2…
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Highly Cited
2001
Highly Cited
2001
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
S. Francke
,
M. Manraj
,
+13 authors
P. Froguel
Human Molecular Genetics
2001
Corpus ID: 37331814
Prevalence of coronary heart disease (CHD), of type 2 diabetes (T2DM) and of the metabolic syndrome are in Mauritius amongst the…
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Highly Cited
2001
Highly Cited
2001
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
P. Leegwater
,
Gerre Vermeulen
,
+13 authors
M. Knaap
Nature Genetics
2001
Corpus ID: 20313523
Leukoencephalopathy with vanishing white matter (VWM) is an inherited brain disease that occurs mainly in children. The course is…
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Highly Cited
2000
Highly Cited
2000
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.
P. Ianakiev
,
M. Kilpatrick
,
I. Toudjarska
,
D. Basel
,
P. Beighton
,
P. Tsipouras
American Journal of Human Genetics
2000
Corpus ID: 45776416
Split-hand/split-foot malformation (SHFM), a limb malformation involving the central rays of the autopod and presenting with…
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Highly Cited
2000
Highly Cited
2000
Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.
A. Kissebah
,
G. Sonnenberg
,
+10 authors
A. Comuzzie
Proceedings of the National Academy of Sciences…
2000
Corpus ID: 16215003
Recent research has emphasized the importance of the metabolic cluster, which includes glucose intolerance, dyslipidemia, and…
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Highly Cited
1994
Highly Cited
1994
Molecular cloning and chromosomal localization of the human thrombopoietin gene
Y. Sohma
,
H. Akahori
,
+6 authors
Hiroshi Miyazaki
FEBS Letters
1994
Corpus ID: 30655651
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