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16q13

A chromosome band present on 16q
National Institutes of Health

Related topics

Related topics

10 relations
16qCCL17 wt AlleleCCL22 wt AlleleCX3CL1 wt Allele

Papers overview

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2019
2019
The effect of CTCF binding sites destruction by CRISPR/Cas9 on transcription of metallothionein gene family in liver hepatocellular carcinoma.
2015
2015
Matrix Metalloproteinase-2 Polymorphisms and Incident Coronary Artery Disease
AbstractPrevious studies have yielded controversial results related to the contribution of matrix metalloproteinase-2 (MMP-2… 
2004
2004
Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
Review
1998
Review
1998
Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature.
Tissue from 14 uterine tumor samples from eight patients-four with endometrial stromal sarcoma (ESS), two with leiomyosarcoma… 
1997
1997
Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13.
Nomiyama, Hisayuki ; Imai, Toshio ; Kusuda, Jun ; Miura, Retsu ; Callen, David F. ; Yoshie, Osamu 
1997
1997
Gene structure, promoter activity, and chromosomal location of the DR-nm23 gene, a related member of the nm23 gene family.
DR-nm23 cDNA was cloned recently by differential screening of a cDNA library derived from chronic myelogenous leukemia-blast… 
Highly Cited
1996
Highly Cited
1996
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
Abstract. Gitelman syndrome is a mostly autosomal recessive disorder affecting the renal tubular function associated with… 
1996
1996
COFS syndrome with familial 1;16 translocation
We report on an Egyptian girl with phenotypic abnormalities of cerebro‐oculo‐facio‐skeletal syndrome. She had microcephaly… 
1995
1995
A constitutional bws‐related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in wilms' tumors
Beckwith‐Wiedemann syndrome (BWS) is a congenital overgrowth disorder with a varying spectrum of clinical manifestations… 
1988
1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.
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