Alterations of Copy Number of Methylation Pattern in Mismatch Repair Genes by Methylation Specific-Multiplex Ligation-Dependent Probe Amplification in Cases of Colon Cancer

Alterations of Copy Number of Methylation Pattern in Mismatch Repair Genes by Methylation Specific-Multiplex Ligation-Dependent Probe Amplification in Cases of Colon Cancer

Bibliographic Details
Main Authors:	Onrat S, Çeken I, Ellidokuz E, Kupelioğlu A
Format:	Article
Language:	English
Published:	Sciendo 2011-01-01
Series:	Balkan Journal of Medical Genetics
Subjects:	colon cancer methylation specificmultiplex ligation-dependent probe amplification (ms-mlpa) mismatched repair (mmr) genes methylation copy number
Online Access:	https://doi.org/10.2478/v10034-011-0044-x

Similar Items

Clinical experience with multiplex ligation-dependent probe amplification for microdeletion syndromes in prenatal diagnosis: 7522 pregnant Korean women
by: Dongsook Lee, et al.
Published: (2019-02-01)

Rapid Identification of Key Copy Number Alterations in B- and T-Cell Acute Lymphoblastic Leukemia by Digital Multiplex Ligation-Dependent Probe Amplification
by: Deepshi Thakral, et al.
Published: (2019-09-01)

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations
by: Chih-Ping Chen, et al.
Published: (2011-03-01)

A Pilot Study of Multiplex Ligation-Dependent Probe Amplification Evaluation of Copy Number Variations in Romanian Children with Congenital Heart Defects
by: Alexandru Cristian Bolunduț, et al.
Published: (2024-02-01)

Multiplex ligation-dependent probe amplification – a short overview
by: Moldovan Valeriu, et al.
Published: (2020-04-01)

Molecular Diagnostics of Duchenne/Becker Muscular Dystrophy Patients by Multiplex Ligation-Dependent Probe Amplification Analysis and Direct Sequencing
by: Todorova A, et al.
Published: (2009-01-01)

Detecting copy number variation in next generation sequencing data from diagnostic gene panels
by: Ashish Kumar Singh, et al.
Published: (2021-08-01)

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children
by: Islam M. Fadel, et al.
Published: (2021-07-01)

The Prevalence of P53 Mutations in Laryngeal Cancer in Kerman
by: M.A Damghani, et al.
Published: (2012-02-01)

Multiplex Ligation-Dependent Probe Amplification for Simultaneous Detection of Six Allergenic Ingredients in Foods
by: WANG Mingqiu, LIU Yan, LI Shiyao, DONG Wanting, ZHANG Tao, LIN Jin, ZHU Biting, ZHANG Li
Published: (2023-02-01)

Hereditary Neuropathy with Liability to Pressure Palsy: A Case Diagnosed with a Quick Multiplex Ligation-dependent Probe Amplification Test
by: Seda Kanmaz, et al.
Published: (2019-06-01)

DNA methylation analysis
by: Thomas von Känel, et al.
Published: (2013-05-01)

Corrigendum: Methylation Statuses of H19DMR and KvDMR at WT2 in Wilms Tumors in Taiwan
by: Meng-Yao Lu, et al.
Published: (2022-08-01)

Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?
by: Africa Manero-Azua, et al.
Published: (2023-10-01)

Multiplex Ligation Dependent Probe Amplification Based Mutation Analysis of Dystrophin Gene in Nepalese Patients with Duchenne Muscular Dystrophy
by: Kushal Shrestha, et al.
Published: (2016-12-01)

Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature
by: Ola M. Eid, et al.
Published: (2020-09-01)

Genotype-phenotype correlation in 22q11.2 deletion syndrome
by: Michaelovsky Elena, et al.
Published: (2012-12-01)

Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report
by: Chih-Hsuan Fu, et al.
Published: (2015-08-01)

Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients
by: Leila C.A. Cardoso, et al.
Published: (2012-01-01)

Characterization of alpha thalassemic genotypes by multiplex ligation-dependent probe amplification in the Brazilian population
by: C.N. Suemasu, et al.
Published: (2011-01-01)

LAMPS: an analysis pipeline for sequence-specific ligation-mediated amplification reads
by: Christopher J. F. Cameron, et al.
Published: (2020-06-01)

Multiplex ligation dependent probe amplification - A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect
by: Crauciuc George Andrei, et al.
Published: (2018-10-01)

Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency
by: Rosa Cifuentes, et al.
Published: (2023-03-01)

Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization
by: Wen-Xu Yang, et al.
Published: (2016-01-01)

16P Subtelomeric Duplication With Vascular Anomalies: An Albanian Case Report And Literature Review
by: Babameto-Laku A., et al.
Published: (2012-12-01)

Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients
by: Natália O. Mota, et al.
Published: (2017-10-01)

Maternally inherited Leigh syndrome detected by Multiplex ligation-dependent probe amplification
by: Lía Mayorga, et al.
Published: (2019-01-01)

Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset
by: Nayereh Nouri, et al.
Published: (2014-01-01)

DNA Mismatch Repair Proteins and BRAF V600E Detection by Immunohistochemistry in Colorectal Cancer Demonstrates Concordance with Next Generation Sequencing
by: Joel Yambert, et al.
Published: (2022-12-01)

Multiplex Ligation-Dependent Probe Amplification for Simultaneous Identification of Bungarus multicinctus and Its Common Adulterants in a Single Assay
by: Yuxin Zhou, et al.
Published: (2020-04-01)

Novel method for the genomic analysis of PKD1 mutation in autosomal dominant polycystic kidney disease
by: Shunlai Shang, et al.
Published: (2023-01-01)

Proximity ligation <it>in situ </it>assay for monitoring the global DNA methylation in cells
by: Vallette François M, et al.
Published: (2011-04-01)

Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype
by: Maria Mabyalwa Mudau, et al.
Published: (2024-03-01)

A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies
by: Anna Minaidou, et al.
Published: (2022-12-01)

Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadism
by: Ja Hye Kim, et al.
Published: (2023-04-01)

Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia
by: Chih-Ping Chen, et al.
Published: (2014-03-01)

Mitochondrial DNA oxidation, methylation, and copy number alterations in major and bipolar depression
by: Deniz Ceylan, et al.
Published: (2023-12-01)

Copy Number Variations and Gene Mutations Identified by Multiplex Ligation-Dependent Probe Amplification in Romanian Chronic Lymphocytic Leukemia Patients
by: Beata Balla, et al.
Published: (2023-08-01)

“Missing mutations” in MPS I: Identification of two novel copy number variations by an IDUA‐specific in house MLPA assay
by: Amir Jahic, et al.
Published: (2019-09-01)

DNA methylation profiles unique to Kalahari KhoeSan individuals
by: Alexander Goncearenco, et al.
Published: (2021-05-01)