Results 131 to 140 of about 18,361 (285)

Detection of Genetic Alterations in Oral Squamous Cell Carcinoma Using Multiplex Ligation-Dependent Probe Amplification (MLPA)

, 2022
Zachary Wei Ern Yong, Lee Peng Karen‐Ng, Thomas George Kallarakkal, Zainal Ariff Abdul Rahman, Siti MazlipahIsmail Ismail, Mannil Thomas Abraham, Keng Kiong Tay, Rosnah Binti Zain, Zuraiza Mohamad Zaini   +8 more
openalex   +2 more sources

Imunodiagnostik Penyakit Kusta

JKS (Jurnal Kedokteran Syiah Kuala), 2006
Abstrak.  Respon  imun pada penyakit  kusta  sangat kompleks    yaitu  melibatkan    imunitas    seluler  dan humoral.    Sebagian    besar  gejala  dan  komplikasi     penyakit   ini   disebabkan   oleh   reaksi  imunologi terhadap  antigen  yang ...
Mudatsir Mudatsir
doaj  

Caracterização dos genótipos da talassemia alfa delecional por MLPA (Multiplex Ligation-Dependent Probe Amplification)

, 2010
C.N. Suemasu
openalex   +1 more source

Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test

Molecular Syndromology, 2017
Rejane A C Monteiro, M. L. de Freitas, G. Vianna, V. T. de Oliveira, Rafaella X. Pietra, L. C. Ferreira, Patrícia P O Rocha, Michele da S. Gonçalves, Giovana da C. César, Joziele de S. Lima, P. F. Medeiros, J. Mazzeu, F. Jehee   +12 more
semanticscholar   +1 more source

Differences in RT-MLPA gene expression levels in progressors and non-progressors.

, 2015
Jayne S. Sutherland, Philip C. Hill, Ifedayo Adetifa, Bouke C. de Jong, Simon Donkor, Simone A. Joosten, Lizet Opmeer, Mariëlle C. Haks, Tom H. M. Ottenhoff, Richard A. Adegbola, Martin O. C. Ota   +10 more
openalex   +2 more sources

Detection of exon 9 deletion by MLPA

, 2011
J.W. Redeker Egbert, S.H. de Visser Annette, A.B. Bergen Arthur, M.A.M. Mannens Marcel   +3 more
openalex   +1 more source

Konjenital Adrenal Hiperplazi Vakalarında CYP21A2 Geni Kopya Sayısı Değişimlerinin MLPA Tekniği İle İncelenmesi

, 2020
Bakhtiyar Mammadov, Aysel Kalaycı Yiğin, Filiz Özdemir, Ahmet Özaydın, Mehmet Seven   +4 more
openalex   +2 more sources

Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA

BMJ Case Reports
T. Todorov, A. Todorova, A. Kirov, B. Dimitrov, R. Carvalho, A. Nygren, I. Boneva, V. Mitev   +7 more
semanticscholar   +1 more source

Comparison of MLPA Method for Detection of Known and Unknown Deletions in Beta Globin Gene Cluster with Old Methods (REAL-TIME, RFLP, Gap-PCR)

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2008
Background and Objectives Thalassaemia is one of the most common single gene disorders, which is most prevalent in the Mediterranean, the Middle East, Indian subcontinent (malaria belt). One of the mutations that result in Thalassaemia is the deletion in
R R Alimohammadi, M Raiesi, A Ebrahimi, S Fallah, S Kianfar, M Masoudifar, S Jamali, S Babashah, M Karimipour, R Mahdian, S Zeinali   +10 more
doaj  

Improving the identification of mody mutations by using mlpa technique in the molecular diagnostics routine [PDF]

, 2015
Renata P. Dotto, Andréia Latanza Gomes Mathez, Luciana F. Franco, João Roberto de Sá, Letícia Schwerz Weinert, Sandra Pinho Silveiro, Fernando de Mello Almada Giuffrida, Magnus R. Dias‐da‐Silva, André F. Reis   +8 more
openalex   +1 more source