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3q28

A chromosome band present on 3q
National Institutes of Health

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6 relations
ChromosomesEIF4A2 wt AlleleETV5 wt AlleleGMNC wt Allele

Papers overview

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Review
2016
Review
2016
An Overview of Genetic Polymorphism and Lung Cancer Risk
The incidence and mortality rates of lung cancer in Asia have increased over the past few decades. Owing to the development of… 
2014
2014
Abstract 942: Imputation from The 1000 Genomes Project identifies rare large effect variants of BRCA2-K3326X and CHEK2-I157T as risk factors for lung cancer; a study from the TRICL consortium
We conducted imputation to The 1000 Genomes Project of genome-wide association studies of lung cancer in populations of European… 
2013
2013
Association of variation in the CLDN1 gene with atopic dermatitis in a German case-control cohort
cohort, were genotyped in 451 unrelated Atopic dermatitis patients and 375 non-atopic controls by means of restriction enzyme… 
2012
2012
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia
A recent genome-wide association study (GWAS) of subjects from Japan and South Korea reported a novel association between the… 
2006
2006
[Urotensin II and somatostatin: two old cousins get together again].
> L’urotensine II (UII) est un neuropeptide cyclique qui a été initialement isolé à partir de l’urophyse1 (➜) des poissons tél… 
Review
2001
Review
2001
Fuzzy Logic in Mitochondrial Locomotion
A review of: Delettre C, Lenaers G, Griffoin J-M, Gigarel N, Lorenzo C, Belenguer P, Pelloquin L, Grosgeorge J, Turc-Carel C… 
2001
2001
KUOPION YLIOPISTO UNIVERSITY OF KUOPIO
Alzheimer’s disease (AD) is the most common cause of progressive neurological disorder leading to dementia. It is… 
1998
1998
Etude clinique et analyse de liaison au locus 3q28 de deux families suisses avec atrophie optique dominante de Kjer (OPA1)
Methoden Resultate Schlußfolgerungen Method Results Conclusions 
1997
1997
Genomic mapping of Kjer Dominant Optic Atrophy.
Kjer DOMINANToptic atrophy (DOA) is a rare primary degeneration of the retinal ganglion cell. In this issue of theArchives, 2… 
1994
1994
No uniparental disomy for chromosome 3 in Brachmann-De Lange syndrome.
Brachmann-De Lange syndrome (BDLS, MIM No. 122470) is a well-described genetic syndrome of mental retardation and multiple… 
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