نتایج جستجو برای: multiplex ligation dependentprobe amplification

تعداد نتایج: 97340  

Journal: :genetics in the 3rd millennium 0
raheleh vazehan zohreh fattahi mahsa fadaee elham parsimehr mehrshid faraji mona montajebiniat

charcot-marie-tooth disease (cmt) is the most common inherited neurological disorder, affecting both motor and sensory peripheral nerves. neurophysiological patterns divide cmt into three main groups: demyelinating cmt1 (upper limb motor nerve conduction velocity (mncv) <38 m/s), axonal cmt2 (mncv >38 m/s) and intermediate cmt (mncv 25-45 m/s). cmt has been also categorized based on the mode of...

Journal: :The Journal of Molecular Diagnostics 2006

Journal: :Croatian medical journal 2006
Alenka Erjavec-Skerget Spela Stangler-Herodez Andreja Zagorac Boris Zagradisnik Nadja Kokalj-Vokac

AIM To identify cryptic subtelomeric rearrangement, a possible cause of idiopathic mental retardation by means of multiprobe telomere fluorescent in situ hybridization (T-FISH). METHODS Hundred patients (median age 3.0 years) with mental retardation and dysmorphic features were screened using specific T-FISH probes. Multiplex ligation-dependent probe amplification and comparative genomic hybr...

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2014
Naoki Uno Katsunori Yanagihara

Multiplex ligation-dependent probe amplification (MLPA) is a widely used technique for detecting genomic structural variants. The technique is based on hybridization and ligation, followed by amplification of the ligation products. Therefore, ligation is considered a fundamental process that determines the feasibility and fidelity of MLPA. However, despite the widespread use of this technique, ...

Elmira Ebrahimi, Kimia Ghaffari, Mehrdad Hashemi, Reza Shirkoohi,

Background: Baculoviral inhibitor of apoptosis repeat-containing 5 (BIRC5) gene is an inhibitor of apoptosis that expresses in human embryonic tissues but it is absent in most healthy adult tissues. The copy number of BIRC5 has been indicated to be highly increased in tumor tissues; however, its association with the age of onset in breast cancer is not well understood. Methods: Forty tumor tiss...

Journal: :Haematologica 2012
Paola Quarello Emanuela Garelli Alfredo Brusco Adriana Carando Cecilia Mancini Patrizia Pappi Luciana Vinti Johanna Svahn Irma Dianzani Ugo Ramenghi

Diamond-Blackfan anemia is an autosomal dominant disease due to mutations in nine ribosomal protein encoding genes. Because most mutations are loss of function and detected by direct sequencing of coding exons, we reasoned that part of the approximately 50% mutation negative patients may have carried a copy number variant of ribosomal protein genes. As a proof of concept, we designed a multiple...

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