Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

Autor: MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori

Publikováno v: Iranian Journal of Public Health, Vol 40, Iss 2, Pp 34-38 (2011)

"nBackground: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syn­dromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been id

Externí odkaz: https://doaj.org/article/308cfe61f6db4851b9e011e0f8c6f5ee

Detection and Quantization of the Expression of Two mu-Opioid Receptor Splice Variants mRNA (hMOR-1A and hMOR-1O) in Peripheral Blood Lymphocytes of Long-Term Abstinent Former Opioid Addicts

Autor: N Vousooghi, F Roushanzamir, A Goodarzi, T Sedaghati, MR Zarrindast, MR Noori Daloii

Publikováno v: Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, Vol 2, Iss 2, Pp 9-14 (2008)

Background and Objectives The mu-Opioid receptor (MOR) exerts a critical role on effects of opiodis. The objective of this study is to find a peripheral bio-marker in addiction studies through quantization of the expression of two MOR splice variants

Externí odkaz: https://doaj.org/article/43c2675490064773835fbe490890e02c

Upregulation of MTOR, RPS6KB1, and EIF4EBP1 in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls.

Autor: Akbarian F; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Poursina St., Tehran, 14155-6447, Iran., Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran., Shaygannejad V; Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Shahpouri MM; Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran., Badihian N; Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran., Sajjadi R; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran., Dabiri A; Department of Immunology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran., Jalilian N; Department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran., Noori-Daloii MR; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Poursina St., Tehran, 14155-6447, Iran. nooridaloii@sina.tums.ac.ir.

Publikováno v: Metabolic brain disease [Metab Brain Dis] 2020 Dec; Vol. 35 (8), pp. 1309-1316. Date of Electronic Publication: 2020 Aug 18.

Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.

Autor: Sobhani M; Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran., Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran., Ghafouri-Fard S; Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Rajab A; Iranian Diabetes Society, Tehran, Iran., Hojjat A; Pediatric Urology Research Center, Department of Pediatric Urology, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran., Kajbafzadeh AM; Pediatric Urology Research Center, Department of Pediatric Urology, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran., Noori-Daloii MR; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. mohrezanoori@yahoo.com.

Publikováno v: BMC medical genetics [BMC Med Genet] 2020 Jan 14; Vol. 21 (1), pp. 13. Date of Electronic Publication: 2020 Jan 14.

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.

Autor: Pourreza MR; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran., Sobhani M; Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran., Rahimi A; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran., Aramideh M; Department of Medicinal Chemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran., Kajbafzadeh AM; Pediatric Urology Research Center, Department of Pediatric Urology, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran., Noori-Daloii MR; Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran. nooridaloii@sina.tums.ac.ir.; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. nooridaloii@sina.tums.ac.ir., Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran. tabatabaiefar@med.mui.ac.ir.; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran. tabatabaiefar@med.mui.ac.ir.

Publikováno v: Acta diabetologica [Acta Diabetol] 2020 Jan; Vol. 57 (1), pp. 81-87. Date of Electronic Publication: 2019 Jul 15.