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4q35

A chromosome band present on 4q
National Institutes of Health

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5 relations
ChromosomesFAT wt AlleleKLKB1 wt AlleleSLC25A4 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Round cell sarcomas beyond Ewing: emerging entities
Primitive small blue round cell tumours (SBRCT) of childhood and young adults have been problematic to diagnose and classify… 
Highly Cited
2007
Highly Cited
2007
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
Autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) is mainly characterized by progressive wasting and weakness of… 
Highly Cited
2007
Highly Cited
2007
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
Highly Cited
2003
Highly Cited
2003
Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress
Highly Cited
2002
Highly Cited
2002
Inappropriate Gene Activation in FSHD A Repressor Complex Binds a Chromosomal Repeat Deleted in Dystrophic Muscle
Highly Cited
2000
Highly Cited
2000
Significant evidence for linkage of mite-sensitive childhood asthma to chromosome 5q31-q33 near the interleukin 12 B locus by a genome-wide search in Japanese families.
Childhood-onset asthma is frequently found in association with atopy. Although asthmatic children may develop IgE antibodies… 
Highly Cited
1999
Highly Cited
1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype
Genotype analysis by using the p13E‐11 probe and other 4q35 polymorphic markers was performed in 122 Italian facioscapulohumeral… 
Highly Cited
1996
Highly Cited
1996
Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).
The p13E-11 probe has been shown to detect DNA rearrangements in sporadic and familial cases of FSHD. Its use, however, has been… 
Highly Cited
1995
Highly Cited
1995
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular…
In facioscapulohumeral muscular dystrophy (FSHD), the wide range of clinical severity observed both within and between families… 
Highly Cited
1992
Highly Cited
1992
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder which maps to chromosome 4qter… 
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