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10q25.1

A chromosome band present on 10q
National Institutes of Health

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10qChromosomesDCLRE1A wt AlleleNEURL wt Allele

Papers overview

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2013
2013
Integrated Analysis Of Genomic and Gene Expression Profiles In Follicular Lymphoma Reveals Subsets and Driver Genes Of Potential Microenvironmental Importance
Background The immune microenvironment in follicular lymphoma (FL) impacts its clinical course, but the interaction between FL… 
Review
2011
Review
2011
Loss of heterozygosity on chromosome 10q in glioblastomas, and its association with other genetic alterations and survival in Indian patients.
BACKGROUND Glioblastoma multiforme (GBM) is the most common malignant central nervous system neoplasm. Loss of heterozygosity… 
2011
2011
S01. Ptosis, arched eyebrows, hypernasal speech, obesity and mild learning disability - a clinical & mapping study.
We report 15 members of a three generation pedigree with ptosis, velopharyngeal incompetence, dysmorphism and a learning… 
2010
2010
Neuralized1 causes apoptosis and downregulates Notch target genes in medulloblastoma.
Neuralized (Neurl) is a highly conserved E3 ubiquitin ligase, which in Drosophila acts upon Notch ligands to regulate Notch… 
2009
2009
Linkage analysis of albuminuria.
American Indians have a higher prevalence of albuminuria than the general population, likely resulting from a combination of… 
2008
2008
Prenatal diagnosis of concomitant Wolf–Hirschhorn syndrome and split hand‐foot malformation associated with partial monosomy 4p (4p16.1→pter) and partial trisomy 10q (10q25.1→qter)
Highly Cited
2006
Highly Cited
2006
Array CGH analysis of pediatric medulloblastomas
Brain tumors are the second most common childhood cancer. We used high‐resolution array comparative genomic hybridization (aCGH… 
2005
2005
Fine mapping of chromosome 10q deletions in mycosis fungoides and sezary syndrome: Identification of two discrete regions of deletion at 10q23.33–24.1 and 10q24.33–25.1
Previous cytogenetic studies in mycosis fungoides (MF) and Sezary syndrome (SS) have identified a large and poorly defined area… 
2003
2003
Single Nucleotide Polymorphism Study of IDDM 17 in a Bedouin Arab Family
Abstract: Type 1 diabetes is an autoimmune disease caused by a combination of genetic and environmental factors. On the basis of… 
2002
2002
Analysis of the Human 3’-Phosphoadenosine 5’-Phosphosulfate Synthase Genes
INTRODUCTION. PAPS is the universal sulfonate donor compound. PAPS synthase (PAPSS) catalyzes the formation PAPS in two concerted… 
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