نتایج جستجو برای: polymorphic trinucleotide

تعداد نتایج: 27186  

Journal: :Methods in molecular biology 2014
D Dafydd Jones James A J Arpino Amy J Baldwin Matthew C Edmundson

This chapter introduces a set of transposon-based methods that were developed to sample trinucleotide deletion, trinucleotide replacement, and domain insertion. Each approach has a common initial step that utilizes an engineered version of the Mu transposon called MuDel. The inherent low sequence specificity of MuDel results in its random insertion into target DNA during in vitro transposition....

Journal: :Parkinsonism & related disorders 2014
Emil Ygland Franco Taroni Cinzia Gellera Serena Caldarazzo Morten Duno Maria Soller Andreas Puschmann

BACKGROUND Compound heterozygosity for a trinucleotide repeat expansion and a point mutation in the FXN gene is a rare cause of Friedreich ataxia (FRDA). METHODS We identified three Swedish FRDA patients with an FXN p.R165P missense mutation and compared their clinical features with six homozygote trinucleotide repeat expansion carriers. Patients were assessed clinically. Trinucleotide expans...

Expressed sequence tags simple sequence repeats (EST-SSRs) are important sources for investigation of genetic diversity and molecular marker development. Similar to genomic SSRs, the EST-SSRs are useful markers for many applications in genetics and plant breeding such as genetic diversity analysis, molecular mapping and cross-transferability across related species and genera. In spite of low po...

Journal: :Asian journal of andrology 2007
Singh Rajender Lalji Singh Kumarasamy Thangaraj

Androgen receptor (AR) gene has been extensively studied in diverse clinical conditions. In addition to the point mutations, trinucleotide repeat (CAG and GGN) length polymorphisms have been an additional subject of interest and controversy among geneticists. The polymorphic variations in triplet repeats have been associated with a number of disorders, but at the same time contradictory finding...

2007
Ilia Anna Serra Gabriele Procaccini Maria Carmela Intrieri Marianna Migliaccio Silvia Mazzuca Anna Maria Innocenti

Posidonia oceanica is an endemic seagrass species in the Mediterranean Sea. Due to its ecological importance, it has been the subject of several genetic studies aimed at increasing general knowledge of the system and helping to define appropriate management strategies. We compared the efficiency of 2 different classes of molecular markers, ‘inter simple sequence repeats’ (ISSRs) and ‘simple seq...

2015
Isabel A. S. Bonatelli Bryan C. Carstens Evandro M. Moraes Swarup Kumar Parida

Microsatellite markers (also known as SSRs, Simple Sequence Repeats) are widely used in plant science and are among the most informative molecular markers for population genetic investigations, but the development of such markers presents substantial challenges. In this report, we discuss how next generation sequencing can replace the cloning, Sanger sequencing, identification of polymorphic lo...

2015
Saeid Reza Khatami Hamid Galehdari Abdorrahman Rasekh Hayat Mombeini Elham Konar

BACKGROUND The androgen receptor (AR) gene contains a polymorphic trinucleotide repeat that encodes a polyglutamine tract in its N-terminal transactivation domain (N- TAD). We aimed to find a correlation between the length of this polymorphic tract and azoospermia or oligozoospermia in infertile men living in Khuzestan, Iran. MATERIALS AND METHODS In this case-control study during two years t...

2008
Zhenkang Xu Laura Gutierrez Matthew Hitchens Steve Scherer Amy K. Sater Dan E. Wells

The results of our bioinformatics analysis have found over 91,000 di-, tri-, and tetranucleotide microsatellites in our survey of 25% of the X. tropicalis genome, suggesting there may be over 360,000 within the entire genome. Within the X. tropicalis genome, dinucleotide (78.7%) microsatellites vastly out numbered tri- and tetranucleotide microsatellites. Similarly, AT-rich repeats are overwhel...

Journal: :Journal of medical genetics 1993
M C Hirst S J Knight Z Christodoulou P K Grewal J P Fryns K E Davies

The fragile X syndrome is a common cause of mental impairment. In view of the low reproductive fitness of affected males, the high incidence of the syndrome has been suggested to be the result of a high rate of new mutations occurring exclusively in the male germline. Extensive family studies, however, have failed to identify any cases of a new mutation. Alternatively, it has been suggested tha...

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