نتایج جستجو برای: multiplex ligation

تعداد نتایج: 42263  

2007
A De Luca V Lanari L Bernardini L Divona S Giustini L Sinibaldi A Novelli I Torrente A Schirinzi B Dallapiccola

A De Luca, I Bottillo, M C Dasdia, A Morella, V Lanari, L Bernardini, L Divona, S Giustini, L Sinibaldi, A Novelli, I Torrente, A Schirinzi, B Dallapiccola . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ....

2013
Shuangrong Jia Feng Wang Fake Li Kai Chang Shaojun Yang Kejun Zhang Wenbin Jiang Ya Shang Shaoli Deng Ming Chen

Journal: :Haematologica 2006
Arjan Buijs Pieter Jaap Krijtenburg Ellen Meijer

We performed genomic profiling using multiplex ligation-dependent probe amplification (MLPA) in 54 cases with suspected or advanced chronic lymphocytic leukemia (CLL). MLPA detected abnormalities when the percentage of mutated cells was greater than approximately 35%. Loss of 9p21 CDNK2A/B was revealed. MLPA is an economically attractive, powerful tool in trial-based, centralized risk-assessmen...

2013
Chunxiu Gong Ming-Qiang Zhu Di Wu Bingyan Cao

Methods 20 SRS cases diagnosed in Beijing Children’s Hospital from 2006 to 2011 were studied retrospectively for clinical manifestations, physical signs, laboratory examinations and respond of GH treatment. We compared with 3 different diagnostic criteria and used the methylationspecific multiplex ligation dependent probe amplification (MS-MLPA) method to detect the chromosome 11p15 imprinting ...

2011
Tae-Jin Song Kyung-A Lee Seong-Woong Kang Hanna Cho Young-Chul Choi

Duchenne muscular dystrophy usually affects males. However, females are also affected in rare instances. Approximately 8% of female Duchenne muscular dystrophy (DMD) carriers are manifesting carriers and have muscle weakness to some extent. We investigated the clinical features of 3 female patients with dystrophinopathy diagnosed by clinical, pathological, and genetic studies at our neuromuscul...

Journal: :Neurology 2006
J C Mulley P Nelson S Guerrero L Dibbens X Iona J M McMahon L Harkin J Schouten S Yu S F Berkovic I E Scheffer

We examined cases of severe myoclonic epilepsy of infancy (SMEI) for exon deletions or duplications within the sodium channel SCN1A gene by multiplex ligation-dependent probe amplification. Two of 13 patients (15%) who fulfilled the strict clinical definition of SMEI but without SCN1A coding or splicing mutations had exonic deletions of SCN1A.

2017
Woong Choi Jongseok Lee Eunjin Cho Gyoo Yeol Jung

Tuberculosis (TB) has severely threatened public health via emerging multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mycobacterium tuberculosis (MTB) strains. For effective TB treatment, rapid, accurate, and multiplex detection of drug resistance is extremely important. However, conventional methods for TB diagnosis are time consuming and have a limited effect on treatment. Nucle...

2017
Évelin Aline Zanardo Roberta Lelis Dutra Flavia Balbo Piazzon Alexandre Torchio Dias Gil Monteiro Novo-Filho Amom Mendes Nascimento Marília Moreira Montenegro Jullian Gabriel Damasceno Fabrícia Andreia Rosa Madia Thaís Virgínia Moura Machado da Costa Maria Isabel Melaragno Chong Ae Kim Leslie Domenici Kulikowski

OBJECTIVE The human genome contains several types of variations, such as copy number variations, that can generate specific clinical abnormalities. Different techniques are used to detect these changes, and obtaining an unequivocal diagnosis is important to understand the physiopathology of the diseases. The objective of this study was to assess the diagnostic capacity of multiplex ligation-dep...

Journal: :Circulation 2011
Moniek G P J Cox Paul A van der Zwaag Christian van der Werf Jasper J van der Smagt Maartje Noorman Zahir A Bhuiyan Ans C P Wiesfeld Paul G A Volders Irene M van Langen Douwe E Atsma Dennis Dooijes Arthur van den Wijngaard Arjan C Houweling Jan D H Jongbloed Luc Jordaens Maarten J Cramer Pieter A Doevendans Jacques M T de Bakker Arthur A M Wilde J Peter van Tintelen Richard N W Hauer

BACKGROUND Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an autosomal dominant inherited disease with incomplete penetrance and variable expression. Causative mutations in genes encoding 5 desmosomal proteins are found in ≈50% of ARVD/C index patients. Previous genotype-phenotype relation studies involved mainly overt ARVD/C index patients, so follow-up data on relatives...

Journal: :Animal genetics 2000
L Karim W Coppieters L Grobet A Valentini M Georges

We herein describe a procedure that allows for simultaneous genotyping of six loss-of-function mutations in the bovine myostatin gene associated with the double-muscling phenotype. The proposed method relies on a multiplex oligonucleotide ligation assay and detection of the fluorescently labelled products using automatic sequencers.

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