Examples of 'dystrophin gene' in a sentence
Meaning of "dystrophin gene"
dystrophin gene - Dystrophin is a large protein found in muscle tissues that helps stabilize and protect muscle fibers. Mutations in the dystrophin gene can lead to muscular dystrophy, a genetic disorder characterized by progressive muscle weakening and degeneration
How to use "dystrophin gene" in a sentence
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dystrophin gene
The dystrophin gene is the largest gene identified to date.
Many different mutations in the dystrophin gene can lead to a dysfunctional protein.
Somatic gene transfer offers a new approach to replace the defective dystrophin gene.
Mutations in the dystrophin gene result in a failure to produce dystrophin in striated muscles.
Duchenne muscular dystrophy arises from mutations that preclude the synthesis of a functional dystrophin gene product.
Mutations in the dystrophin gene are the cause of DMD.
Errors or mutations in the Dystrophin gene.
The dystrophin gene is the largest gene ever found, and is among the most complex.
DMD is known to be caused by a mutation in the dystrophin gene.
The dystrophin gene is the largest gene in the body, consisting of 79 exons.
BMD results from different mutations in the dystrophin gene.
The dystrophin gene has 79 exons and is therefore up to four times longer.
The DNA in the blood is tested to look at the dystrophin gene.
In children with DMD, the dystrophin gene is corrupt - it contains a genetic defect ( mutation ).
The DMD gene or protein corresponds to the dystrophin gene or protein.
See also
The human dystrophin gene has about 75 exons.
Both DMD and BMD are caused by mutations in the dystrophin gene.
Specifically, exon 53 mutants of the human dystrophin gene include the polynucleotides defined in ( a ) or ( b ) below.
In a preferred embodiment, a functional dystrophin protein means an in frame dystrophin gene.
The nucleotide sequence of human wild-type dystrophin gene is known GenBank Accession No.
A family history, to detect family members who carry the dystrophin gene.
The nucleotide sequence of human wild-type dystrophin gene is known GeneBank Accession No.
In a particularly preferred embodiment said pre-mRNA is derived from a dystrophin gene.
A 1.8 kb fragment of the human dystrophin gene was amplified.
The oligomer of the present invention causes skipping of exon 44 in the dystrophin gene.
In a particularly preferred embodiment of the disclosure said pre-mRNA is derived from a dystrophin gene.
Becker muscular dystrophy ( BMD ) is also caused by a mutation in the dystrophin gene.
Polymerase chain reaction ( PCR ) can detect some mutations in the dystrophin gene.
Duchenne muscular dystrophy ( DMD ) is a serious illness resulting from mutations in the dystrophin gene.
The exon being skipped is exon 44 of the human dystrophin gene.
Duchenne is caused by mutations ( changes ) within the dystrophin gene.
More specifically, the target exon is exon 44 in the human dystrophin gene.
Like deletions, duplications can occur throughout all 79 exons of the dystrophin gene.
The seventh day of the ninth month represent the 79 exons in the dystrophin gene.
The 7th day of the 9th month represents the 79 exons of the dystrophin gene.
Multiplex-PCR was first described in 1988 as a method to detect deletions in the dystrophin gene.
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Examples of using Dystrophin
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Muscles lacking dystrophin develop less tension
The name is a contraction for ubiquitous dystrophin
The subject may be a dystrophin deficient subject
