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2q33.1

A chromosome band present on 2q
National Institutes of Health

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3 relations
ChromosomesHSPD1 wt AlleleSF3B1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Phenotypic and genetic analysis of a sibpair with partial deletion of SATB2 gene caused by 2q33.1 microdeletion].
OBJECTIVE To analyze the genotype and phenotype of a sibpair with partial deletion of SATB2 gene caused by 2q33.1 microdeletion… 
Review
2018
Review
2018
Developmental Defects Associated With DNA Copy Number Gain of Chromosome 2q33.1: A Case Report and Review of Literature.
Caspases play a vital role during apoptosis. In addition to apoptosis, caspases play a role in cytokine gene induction and work… 
2017
2017
Cross-Cancer Analysis Reveals Novel Pleiotropic Associations-Letter.
Meta-analysis of genome-wide association (GWA) studies of cancer susceptibility by Fehringer and colleagues ([1][1]) revealed… 
2015
2015
rs 2294008 PSCA the Yin Yang of biomarkers of gastric cancer susceptibility : Functional annotation of high-quality SNP
Functional annotation of high-quality SNP biomarkers of gastric cancer susceptibility: the Yin Yang of PSCA rs2294008 Dear Editor… 
2014
2014
Cytogenetically normal uterine leiomyomas without MED12-mutations – a source to identify unknown mechanisms of the development of uterine smooth muscle tumors
Recent findings on genetic changes in uterine leiomyomas suggest these benign tumors being a heterogeneous group of diseases in… 
2011
2011
A pathogenic breakpoint at 566.8 kb from the 3′ end of the SATB2 leads to a 2q33.1 microdeletionlike phenotype
Review
2010
Review
2010
Molecular characterization of a new patient with a non‐recurrent inv dup del 2q and review of the mechanisms for this rearrangement
We report on newborn baby with microcephaly, facial anomalies, congenital heart defects, hypotonia, wrist contractures, long… 
2010
2010
Exercise genes? And no, not Levi's 501s!
genetic studies have generally focused on clinical or pathological phenotypes, such as obesity and diabetes. Now accumulating… 
Review
2010
Review
2010
Author's response to reviews Title: A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1 Authors:
1997
1997
Molecular cloning, refined chromosomal mapping and structural analysis of the human gene encoding aldehyde oxidase (AOX1), a candidate for the ALS2 gene.
Aldehyde oxidase (AOX) is a member of the xanthine oxidase (XO) family of molybdenum hydroxylase, iron-sulfur flavoproteins and… 
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