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4q12

A chromosome band present on 4q
National Institutes of Health

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5 relations
CLOCK wt AlleleChromosomesFIP1L1 wt AlleleIGFBP7 wt Allele

Papers overview

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2018
2018
Characterization of 4q12 amplification in 8819 advanced solid tumor cases.
e24275Background: The amplification of chromosomal segment 4q12, which includes three genes (PDGFRA, KIT and KDR), has been… 
Review
2011
Review
2011
RASL11B (RAS-like, family 11, member B)
Review on RASL11B (RAS-like, family 11, member B), with data on DNA, on the protein encoded, and where the gene is implicated. 
2011
2011
The N ×D-BMAP/G/1 Queueing Model: Queue Contents and Delay Analysis
We consider a single-server discrete-time queueing system with N sources, where each source is modelled as a correlated Markovian… 
2011
2011
Leriche’s syndrome and Löffler endocarditis in a 30-year-old patient presenting with hypereosinophilic syndrome
Dear Editor, Here, we report a severe complication of hypereosinophilic syndrome (HES), the onset of Leriche’s syndrome, in a… 
2011
2011
P3-01-11: Increased Gene Copy Number of c-KIT and VEGFR2 at 4q12 in Primary Breast Cancer Is Related to an Aggressive Phenotype and Impaired Prognosis.
Introduction : Triple-negative breast cancer (TNBC) accounts for approximately 15% of all female breast cancer and is associated… 
2008
2008
system involvement leukaemia and associated central nervous positive chronic eosinophilic PDGFRA − FIP 1 L 1
http://jcp.bmj.com/content/61/5/677.full.html Updated information and services can be found at: These include: References http… 
2006
2006
Chronic Eosinophilic Leukemia with the FIP1L1-PDGFR± Fusion Gene in a Patient with a History of Combination Chemotherapy
Hypereosinophilic syndrome (HES) was diagnosed in December 2000 in a 43-year-old man on the basis of persistent eosinophilia (11… 
2005
2005
Genetic mapping and association analysis in multiple sclerosis
Multiple sclerosis (MS) is a chronic neurological disease. Epidemiological studies have shown evidence for both environmental and… 
2003
2003
Clinical characteristics of hypereosinophilic syndromes with an interstitial 4q12 deletion resulting in a FIP1L1-PDGFRA fusion gene
1982
1982
[Monosomy/trisomy 4q12 to q13 mosaicism in a retarded and dysmorphic girl].