Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients.

Autor: Ebrahimi, Milad¹, Behnam, Mahdieh², Behranvand-Jazi, Nafiseh¹, Yari, Ladan³, Sheikh-Kanlomilan, Sajad⁴, Salehi, Mansoor^2,5 m-salehi@med.mui.ac.ir, Tahmasebi, Pardis¹, Amini, Mohaddeseh¹, Behjati, Mohaddeseh⁶, Hosseini, Nafisehsadat⁷

Publikováno v: Journal of Research in Medical Sciences. Aug2017, Vol. 22, p1-3. 3p.

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The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk.

Autor: Mozaffarizadeh H; Department of Genetics, Isfahan University of Medical Sciences, Isfahan, Iran., Mokarian F; Department of Clinical Oncology, Isfahan University of Medical Sciences, Isfahan, Iran., Salehi M; Department of Genetics, Isfahan University of Medical Sciences, Isfahan, Iran., Hakimian SMR; Department of Clinical Oncology, Cancer Prevention Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Moazam E; Department of Clinical Oncology, Cancer Prevention Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Amoozadehsamakoosh A; Faculty of Medicine, Babol University of Medical Sciences, Babol, Iran., Hosseinzadeh M; Department of Genetics, Isfahan University of Medical Sciences, Isfahan, Iran., Behnam M; Department of Genetics, Isfahan University of Medical Sciences, Isfahan, Iran., Behjati M; Department of Medicine, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran., Naseri A; Department of Medical Biotechnology, Faculty of Medicine, Babol University of Medical Sciences, Babol, Iran., Lotfi M; Department of Medical Genetics, Abortion Research Center, Reproductive Sciences Institute, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran., Tohidi F; Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.; Department of Medical Biotechnology, Cancer Research Center, School of Medicine, Babol University of Medical Sciences, Babol, Iran.

Publikováno v: Global medical genetics [Glob Med Genet] 2024 Mar 04; Vol. 11 (1), pp. 69-75. Date of Electronic Publication: 2024 Mar 04 (Print Publication: 2024).

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.

Autor: Nouri N; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran ; Pediatric Inherited Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran ; Pediatric Neurology, Pediatric Neurology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Fazel-Najafabadi E; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran., Salehi M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran ; Department of Genetics and Molecular Biology, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran., Hosseinzadeh M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran., Behnam M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran., Ghazavi MR; Pediatric Neurology, Pediatric Neurology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Sedghi M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran ; Pediatric Inherited Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran ; Pediatric Neurology, Pediatric Neurology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Publikováno v: Advanced biomedical research [Adv Biomed Res] 2014 Jan 27; Vol. 3, pp. 72. Date of Electronic Publication: 2014 Jan 27 (Print Publication: 2014).