نتایج جستجو برای: mlpa

تعداد نتایج: 902  

2013
Farkhondeh Behjati Saghar Ghasemi Firouzabadi Firoozeh Sajedi Kimia Kahrizi Mostafa Najafi Behruz Ebrahimizade Ghasemlou Yousef Shafeghati Fatemeh Behnia Ali Reza Mohammadi Arya Hossein Karimi Fatemeh Hadipour Zahra Hadipour Peyman Jamali Roxana Kariminejad Hossein Darvish Ideh Bahman Eiman Bagherizadeh Hossein Najmabadi Roshanak Vameghi

BACKGROUND Mental retardation/Developmental delay (MR/DD) is present in 1 - 3% of the general population (1, 2). MR is defined as a significant impairment of both cognitive (IQ < 70) and social adaptive functions, with onset before 18 years of age. OBJECTIVES The purpose was to determine the results of subtelomeric screening by the Multiplex Ligation Dependent Probe Amplification (MLPA) Techn...

Journal: :Leprosy review 1992
B Sekar D Anandan

A comparison of the ELISA test with the newly-developed MLPA test was carried out, using eluates of blood spots from filter paper for the detection of the anti-PGL-I antibody. A very good positive correlation was observed between these two tests. The concordance rate was found to be 92.6%, ranging from 71.4% to 100%. This nonconcordance was not found when freshly-collected samples were used. Th...

Journal: :Clinical biochemistry 2006
Kent K S Lai Ivan F M Lo Tony M F Tong Lydia Y L Cheng Stephen T S Lam

OBJECTIVES To evaluate the efficacy of Multiplex Ligation-dependent Probe Amplification (MLPA) technique in comparison with the traditional multiplex PCR assay in detection of exon deletions and duplications of the DMD gene. DESIGN AND METHODS The sensitivity and accuracy of MLPA were assessed and compared with the multiplex PCR in a total of 63 subjects including 43 subjects with Duchenne mu...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2008
Mariana F A Funari Alexander A L Jorge Emilia M Pinto Ivo J P Arnhold Berenice B Mendonca Mirian Y Nishi

LWD is associated to SHOX haploinsufficiency, in most cases, due to gene deletion. Generally FISH and microsatellite analysis are used to identify SHOX deletion. MLPA is a new method of detecting gene copy variation, allowing simultaneous analysis of several regions. Here we describe the presence of a SHOX intragenic deletion in a family with LWD, analyzed through different methodologies. Genom...

2013
Duy Pham Thanh Nga Tran Vu Thieu Chau Tran Thuy Martin Lodén Kiki Tuin James I. Campbell Nguyen Van Minh Hoang Phat Voong Vinh Jeremy J. Farrar Kathryn E. Holt Gordon Dougan Stephen Baker

Salmonella enterica serovar Typhi, the causative agent of typhoid fever, is highly clonal and genetically conserved, making isolate subtyping difficult. We describe a standardized multiplex ligation-dependent probe amplification (MLPA) genotyping scheme targeting 11 key phylogenetic markers of the S. Typhi genome. The MLPA method demonstrated 90% concordance with single nucleotide polymorphism ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علوم بهزیستی و توانبخشی - پژوهشکده علوم بهزیستی 1389

mlpa برای نواحی ساب تلومریک ابتدا بوسیله کیت salas mlpa kit p036-e1انجام شد ودرمواردی که ناهنجاری تشخیص داده شد برای تایید کیت salas mlpa kit p070-a2 مورد استفاده قرار گرفت دربررسی انجام شده فقط یک بیمار ( 3/3 درصد) ناهنجاری ساب تلومریک داشت که واجد دوپلیکاسیون ناحیه ساب تلومریک بازوی کوتاه کروموزوم p x/yبود . طی آزمایشاتی که بر روی مادر و یکی از فرزنذان خانواده پروباند انجام شد نشان داده شد که...

2015
Tao Wang Yutaka Amemiya Pauline Henry Arun Seth Wedad Hanna Eugene T. Hsieh

Therapy with trastuzumab confers a survival benefit in HER2 positive advanced gastric and gastroesophageal adenocarcinoma. HER2 status is evaluated by immunohistochemistry (IHC) and in situ hybridization (ISH). An ISH ratio of HER2 to centromere 17 (CEP17) ≥2.0 is considered amplified. This assumes that CEP17 reflects chromosomal copy number. Cases where CEP17 exceeds 3 are classified as polyso...

Journal: :BioTechniques 2009
Andrea Perne Xianghong Zhang Lutz Lehmann Marco Groth Frank Stuber Malte Book

The reliable quantification of gene copy number variations is a precondition for future investigations regarding their functional relevance. To date, there is no generally accepted gold standard method for copy number quantification, and methods in current use have given inconsistent results in selected cohorts. In this study, we compare two methods for copy number quantification. beta-defensin...

2012
Leila C.A. Cardoso Jair A. Tenorio Castaño Hanna S. Pereira Maria Angélica de F.D. Lima Anna Cláudia E. dos Santos Paulo S. de Faria Sima Ferman Héctor N. Seuánez Julián B. Nevado José Carlos Cabral de Almeida Pablo Lapunzina Fernando R. Vargas

The most frequent epigenetic alterations in Wilms tumor (WT) occur at WT2, assigned to 11p15. WT2 consists of two domains: telomeric domain 1 (DMRH19) that contains the IGF2 gene and an imprinted maternally expressed transcript (H19) and centromeric domain 2 (KvDMR) that contains the genes KCNQ1, KCNQ1OT1 and CDKN1C. In this work, we used pyrosequencing and MS-MLPA to compare the methylation pa...

Journal: :Human mutation 2003
C F Taylor R S Charlton J Burn E Sheridan G R Taylor

Gene dosage abnormalities account for a significant proportion of the mutations in genes tested in DNA diagnostic laboratories. Detection of these changes has proved a challenge as the methods available to date are time consuming or unreliable. The multiplex ligation-dependent probe assay (MLPA) is a new technique allowing relative quantification of up to 40 different nucleic acid sequences in ...

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