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1q25

A chromosome band present on 1q
National Institutes of Health

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CDC73 wt AlleleChromosomesNCF2 wt AlleleRNASEL wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression
A genome-wide screen was conducted for type 2 diabetes progression genes using measures of elevated fasting glucose levels as… 
2003
2003
Characterization of the ~ 6 7 ~ ~ ' " Gene : Genomic Organization and Restriction Fragment Length Polymorphism Analysis for Prenatal Diagnosis in Chronic Granulomatous Disease
The genetic defect in the p67Pk-deficient form of chronic granulomatous disease (CGD) follows an autosomal recessive pattern of… 
1997
1997
A cytogenetically anchored genetic map of bovine chromosome 1 obtained by integrating flow-sorted chromosome-derived microsatellite markers into the international bovine map.
A genomic library was constructed from a peak of flow-sorted bovine chromosomes 1 + X after PCR amplification. Forty-three bovine… 
Review
1996
Review
1996
New recurrent structural chromosome aberrations in non-Hodgkin's lymphoma.
Identification, and subsequent molecular dissection, of recurring structural chromosome aberrations has led to a substantial… 
1994
1994
Localization of acyl coenzyme A:cholesterol acyltransferase gene to human chromosome 1q25
Acyl coenzyme A:cholesterol acyltransferase (ACAT) is an intracellular enzyme that catalyzes the formation of cholesterol esters… 
1994
1994
Localization of cofilin gene to 1q25
Cofilin is a 21 kD actin-binding protein which has recently been identified as an important intracellular messenger that… 
1994
1994
Polymorphisms in the phosducin (PDC) gene on chromosome 1q25-32
Phosducin (33 kDa protein or MEKA) is a principal water-soluble phosphoprotein in the rod and cone photoreceptor cells and… 
1986
1986
Partial trisomy 1q25----qter.
1979
1979
Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1q.
A newborn female is described who exhibited a characteristic facial dysmorphology including deep-set eyes, broad nasal bridge… 
1979
1979
Use of chromosomal translocations with in situ DNA hybridisation to confirm localisation of human 5S ribosomal RNA genes.
Two cases of chromosomal translocations involving the long arm of chromosome 1 were investigated for 5S ribosomal gene… 
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