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9q31.3

A chromosome band present on 9q.
National Institutes of Health

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Related topics

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Chromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Genetic Polymorphisms within The Intronless ACTL7A and ACTL7B Genes Encoding Spermatogenesis-Specific Actin-Like Proteins in Japanese Males
Actins play essential roles in cellular morphogenesis. In mice, the T-actin1 and 2 genes, which encode actin-like proteins, are… 
2014
2014
Characterization of Human Thioredoxin System and the Potential Cellular Responses Encoded to Observe the Thioredoxin-Trx1 Reversibly Regulated Redox Sites.
Txn1 is a pleiotropic cellular causative gene factor which has numerous functions. Here the following reaction is the possible… 
Highly Cited
2010
Highly Cited
2010
Tumorigenesis and Neoplastic Progression KLF 4 is a Novel Candidate Tumor Suppressor Gene in Pancreatic Ductal Carcinoma
From the Department of Molecular Pharmacology and Chemistry,* Memorial Sloan Kettering Cancer Center, New York, New York; the… 
2009
2009
Molecular Alterations at 9q33.1 and Polyploidy in Asbestos-Related Lung Cancer
Purpose: Asbestos causes DNA damage and the fibers, together with tobacco smoke, have a synergistic effect on lung cancer risk… 
2006
2006
Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome
To present the perinatal findings and the molecular cytogenetic analyses of a de novo interstitial deletion of 9q (9q22.3→q31.3… 
2004
2004
The paternal chromosome 9 and the maternal chromosome 22 are preferentially rearranged in chronic myeloid leukaemia
Correction to: Leukemia (2004) 18, 1445–1448. doi:10.1038/sj.leu.2403404 Due to a typesetting error, the data in Tables 1 and 2… 
2003
2003
Bladder Neoplasms--Regions at Chromosome 9 with Putative Tumour Suppressor Genes
Objectives: To investigate the prevalence of Loss of heterozygosity (LOH) at 12 different loci on chromosome 9 in patients with… 
2001
2001
Cloning, characterization, and genomic structure of the mouse Ikbkap gene.
Our laboratory recently reported that mutations in the human I-kappaB kinase-associated protein (IKBKAP) gene are responsible for… 
1999
1999
Edg‐2 in myelin‐forming cells: Isoforms, genomic mapping, and exclusion in Charcot‐Marie‐Tooth disease
Edg‐2 is an heptahelical receptor whose spatio‐temporal distribution during rat brain development is consistent with a role in… 
1999
1999
Significant differences in the frequency of transcriptional units, types and numbers of repetitive elements, GC content, and the number of CpG islands between a 1010-kb G-band genomic segment on…
We determined the nucleotide sequence of the entire 1,010,525-bp insert contained in CEPH YAC clone 867e8. This human genomic… 
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