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   Articles with "ctg repeat" as a keyword



Highly sensitive MicroRNA 146a detection using a gold nanoparticle-based CTG repeat probing system and isothermal amplification.

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recommendations! Published in 2018 at "Analytica chimica acta"

DOI: 10.1016/j.aca.2017.11.016

Abstract: We have developed a gold nanoparticle (AuNP)-based CTG repeat probing system displaying high quenching capability and combined it with isothermal amplification for the detection of miRNA 146a. This method of using a AuNP-based CTG repeat… read more here.

Keywords: ctg repeat; repeat; probing system; based ctg ... See more keywords
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Single-Tube Dodecaplex PCR Panel of Polymorphic Microsatellite Markers Closely Linked to the DMPK CTG Repeat for Preimplantation Genetic Diagnosis of Myotonic Dystrophy Type 1.

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recommendations! Published in 2017 at "Clinical chemistry"

DOI: 10.1373/clinchem.2017.271528

Abstract: BACKGROUND Preimplantation genetic diagnosis (PGD) of myotonic dystrophy type 1 (DM1) currently uses conventional PCR to detect nonexpanded dystrophia myotonica protein kinase (DMPK) alleles or triplet-primed PCR to detect the CTG-expanded alleles, coupled with analysis… read more here.

Keywords: dmpk ctg; ctg repeat; ctg; panel ... See more keywords
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CTG-Repeat Detection in Primary Human Myoblasts of Myotonic Dystrophy Type 1

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recommendations! Published in 2021 at "Frontiers in Neuroscience"

DOI: 10.3389/fnins.2021.686735

Abstract: Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder caused by unstable CTG-repeat expansions in the DMPK gene. Tissue mosaicism has been described for the length of these repeat expansions. The most obvious… read more here.

Keywords: human myoblasts; ctg repeat; dystrophy type; repeat ... See more keywords
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Overview of the Complex Relationship between Epigenetics Markers, CTG Repeat Instability and Symptoms in Myotonic Dystrophy Type 1

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recommendations! Published in 2022 at "International Journal of Molecular Sciences"

DOI: 10.3390/ijms23073477

Abstract: Among the trinucleotide repeat disorders, myotonic dystrophy type 1 (DM1) is one of the most complex neuromuscular diseases caused by an unstable CTG repeat expansion in the DMPK gene. DM1 patients exhibit high variability in… read more here.

Keywords: dystrophy type; repeat; ctg repeat; repeat instability ... See more keywords