Sirenomelia: two case reports
Shojaee, Asiyeh, Ronnasian, Firooze, Behnam, Mahdiyeh, Salehi, Mansoor
Published in Journal of medical case reports (26.04.2021)
Published in Journal of medical case reports (26.04.2021)
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Journal Article
Identification of disease-causing genes using microarray data mining and Gene Ontology
Mohammadi, Azadeh, Saraee, Mohammad H, Salehi, Mansoor
Published in BMC medical genomics (26.01.2011)
Published in BMC medical genomics (26.01.2011)
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Journal Article
GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants
Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Reiisi, Somayeh, Pourreza, Mohammad Reza, Noori-Daloii, Mohammad Reza, Tabatabaiefar, Mohammad Amin
Published in International journal of pediatric otorhinolaryngology (01.04.2018)
Published in International journal of pediatric otorhinolaryngology (01.04.2018)
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Journal Article
Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients
Nouri, Negar, Mehrzad, Valiollah, Khalaj, Zahra, Zaker, Erfan, Zare, Fateme, Abbasi, Elham, Khosravi, Maede, Kalantar, Seyed Mehdi, Salehi, Mansoor
Published in Egyptian Journal of Medical Human Genetics (01.12.2023)
Published in Egyptian Journal of Medical Human Genetics (01.12.2023)
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Journal Article
Promising effect of rapamycin on multiple sclerosis
Bagherpour, Bahram, Salehi, Mansoor, Jafari, Rasool, Bagheri, Akram, Kiani-Esfahani, Abbas, Edalati, Masoud, Kardi, Mohammad Taghi, Shaygannejad, Vahid
Published in Multiple sclerosis and related disorders (01.11.2018)
Published in Multiple sclerosis and related disorders (01.11.2018)
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Journal Article
Dysregulation of RNA interference components in COVID-19 patients
Mousavi, Seyyed Reza, Sajjadi, Maryam Sadat, Khosravian, Farinaz, Feizbakhshan, Sara, Salmanizadeh, Sharareh, Esfahani, Zahra Taherian, Beni, Faeze Ahmadi, Arab, Ameneh, Kazemi, Mohammad, Shahzamani, Kiana, Sami, Ramin, Hosseinzadeh, Majid, Salehi, Mansoor, Lotfi, Hajie
Published in BMC research notes (29.10.2021)
Published in BMC research notes (29.10.2021)
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Journal Article
A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family
Koohiyan, Mahbobeh, Noori-Daloii, Mohammad Reza, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Tabatabaiefar, Mohammad Amin
Published in Audiology & neurotology (2019)
Published in Audiology & neurotology (2019)
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Journal Article
Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients
Komachali, Sajad Rafiee, Siahpoosh, Zakieh, Komachali, Sara Rafiee, Tamandani, Dor Mohammad Kordi, Salehi, Mansoor
Published in European Journal of Biological Research (01.11.2022)
Published in European Journal of Biological Research (01.11.2022)
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Journal Article
CTNS Mutations Causing Autosomal Recessive Cystinosis in a Subset of Iranian Population: Report of Two New Variants
Mohammadi Chermahini, Zahra, Salehi, Mansoor, Gheissari, Alaleh, Ahmadi Beni, Faeze, Khosravian, Farinaz, Kazemi, Mohammad
Published in Advanced biomedical research (2024)
Published in Advanced biomedical research (2024)
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Journal Article
A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23
Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Noori-Daloii, Mohammad Reza, Tabatabaiefar, Mohammad Amin
Published in Audiology & neurotology (2020)
Published in Audiology & neurotology (2020)
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Journal Article
A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel
Majidzadeh-A, Keivan, Zarinfam, Shiva, Abdoli, Nasrin, Yadegari, Fatemeh, Esmaeili, Rezvan, Farahmand, Leila, Teimourzadeh, Azin, Taghizadeh, Mahdieh, Salehi, Mansoor, Zamani, Mohamad
Published in Familial cancer (01.04.2022)
Published in Familial cancer (01.04.2022)
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Journal Article
Study of The Correlation between miR-106a, miR-125b, and miR-330 on Multiple Sclerosis Patients by Targeting TNFSF4 and SP1 in NF-кb/TNF-α Pathway: A Case-Control Study
Hadi, Nasrin, Seifati, Seyed Morteza, Nateghi, Behnaz, Ravaghi, Parisa, Khosravian, Farinaz, Namazi, Faezeh, Maryam Fotouhi Firouzabad, Shaygannejad, Vahid, Salehi, Mansoor
Published in Cell journal (Yakhteh) (01.07.2022)
Published in Cell journal (Yakhteh) (01.07.2022)
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Journal Article
Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants
Mianesaz, Hamidreza, Ghalamkari, Safoura, Salehi, Mansoor, Behnam, Mahdiyeh, Hosseinzadeh, Majid, Basiri, Keivan, Ghasemi, Majid, Sedghi, Maryam, Ansari, Behnaz
Published in Molecular genetics & genomic medicine (01.02.2023)
Published in Molecular genetics & genomic medicine (01.02.2023)
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Journal Article
A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features
Sekiguchi, Futoshi, Nasiri, Jafar, Sedghi, Maryam, Salehi, Mansoor, Hosseinzadeh, Majid, Okamoto, Nobuhiko, Mizuguchi, Takeshi, Nakashima, Mitsuko, Miyatake, Satoko, Takata, Atsushi, Miyake, Noriko, Matsumoto, Naomichi
Published in Journal of human genetics (01.04.2018)
Published in Journal of human genetics (01.04.2018)
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Journal Article
New long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based study
Abdolvand, Mohammad, Chermahini, Zahra Mohammadi, Bahaloo, Sahar, Emami, Mohammad Hassan, Fahim, Alireza, Rahimi, Hojjatolah, Amjadi, Elham, Maghool, Fatemeh, Rohani, Fattah, Dadkhah, Mina, Farhadian, Nooshin, Vatandoust, Nasimeh, Abdolvand, Shirin, Darehsari, Maliheh Roozbahani, Chehelgerdi, Mohammad, Beni, Faeze Ahmadi, Khodadoostan, Mahsa, Hemati, Simin, Salehi, Mansoor
Published in Journal of research in medical sciences (2024)
Published in Journal of research in medical sciences (2024)
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Journal Article
The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk
Mozaffarizadeh, Hengameh, Mokarian, Fariborz, Salehi, Mansoor, Hakimian, Seyyed Mohammad Reza, Moazam, Elham, Amoozadehsamakoosh, Amirmohammad, Hosseinzadeh, Majid, Behnam, Mahdieh, Behjati, Mohaddeseh, Naseri, Alma, Lotfi, Marzieh, Tohidi, Fatemeh
Published in Global medical genetics (01.01.2024)
Published in Global medical genetics (01.01.2024)
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Journal Article