Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hamideh Bagherian"'
Autor:
Amin Hosseini Nami, Mahboubeh Kabiri, Fatemeh Zafarghandi Motlagh, Tina Shirzadeh, Hamideh Bagherian, Razie Zeinali, Ali Karimi, Sirous Zeinali
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 18 (2024)
Cystic fibrosis (CF) is an autosomal recessive disease caused by the inheritance of two mutant cystic fibrosis transmembrane conductance regulator (CFTR) alleles, one from each parent. Autosomal recessive disorders are rarely associated with germline
Externí odkaz:
https://doaj.org/article/d19607efa82244da81c2219fe49c3f67
Autor:
Amin Hosseini Nami, Mahboubeh Kabiri, Fatemeh Zafarghandi Motlagh, Tina Shirzadeh, Negar Fakhari, Ali Karimi, Hamideh Bagherian, Mojdeh Jamali, Shahrzad Younesikhah, Sara Shadman, Razie Zeinali, Sirous Zeinali
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Objectives: Cystic fibrosis (CF) is the most prevalent autosomal recessive disorder among Caucasians. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause this pathology. We, therefore, aimed to describe the CFTR mut
Externí odkaz:
https://doaj.org/article/12230b9b921343a382486274b6b8f73a
Autor:
Yeganeh Keshvar, Solmaz Sabeghi, Zohreh Sharifi, Kiyana Sadat Fatemi, Panti Fouladi, Shahrzad Younesi Khah, Faezeh Rahiminejad, Atefeh Joudaki, Masoume Amini, Hamideh Bagherian, Marefat Ghaffari Novin, Mansoureh Movahedin, Marzieh Mojbafan, Sirous Zeinali
Publikováno v:
BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background Preimplantation genetic diagnosis (PGD) has been developed to detect genetic disorders before pregnancy which is usually done on blastomeres biopsied from 8-cell stage embryos obtained from in vitro fertilization method (IVF). Her
Externí odkaz:
https://doaj.org/article/21363afe98e74915b267e691cd93b675
Autor:
Sirous Zeinali, Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Soheila Sotoudeh, Hamideh Bagherian, Jouni Uitto
Publikováno v:
International Journal of Dermatology and Venerology, Vol 4, Iss 2, Pp 82-85 (2021)
Abstract. Objective:. Isolated hereditary hypotrichosis is caused by mutations in as many as 11 different genes. The conventional mutation detection strategy consists of sequencing of individual candidate genes separately, a time consuming and costly
Externí odkaz:
https://doaj.org/article/3b59bf5d98ba4093951c096a28afbe2e
Autor:
Thao T. Tran, Rachel B. Keller, Brecht Guillemyn, Melanie Pepin, Jane E. Corteville, Samir Khatib, Mohammad-Sadegh Fallah, Sirous Zeinali, Fransiska Malfait, Sofie Symoens, Paul Coucke, Peter Witters, Elena Levtchenko, Hamideh Bagherian, Deborah A. Nickerson, Michael J. Bamshad, Jessica X. Chong, Peter H. Byers
Publikováno v:
HGG Advances, Vol 2, Iss 4, Pp 100051- (2021)
Summary: The bone disorder osteogenesis imperfecta (OI) is genetically heterogeneous. Most affected individuals have an autosomal dominant disorder caused by heterozygous variants in either of the type I collagen genes (COL1A1 or COL1A2). To date, tw
Externí odkaz:
https://doaj.org/article/48903d8149a8425083091af497e532e3
Autor:
Sanaz Ranjbarrad, Asiyeh Jebelli, Faegheh Sadeghi, Fatemeh Zeinali Sehrig, Mohammad-Sadegh Fallah, Hamideh Bagherian, Tina Shirzadeh, Fatemeh Zafarghandi Motlagh, Leila Emrahi
Background: Congenital cataract (CC) is the most common reason for visual loss and blindness at birth or early childhood worldwide. The autosomal dominant (AD) inheritance is reported as the most frequent transmission pattern for CC. Connexin 46 (Cx4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2e31e0f7328c52f86d205e36a0f7071
https://doi.org/10.21203/rs.3.rs-1851272/v1
https://doi.org/10.21203/rs.3.rs-1851272/v1
Autor:
Soheila Sotoudeh, Amir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, Jouni Uitto, Sirous Zeinali, Hamideh Bagherian
Publikováno v:
International Journal of Dermatology and Venerology, Vol 4, Iss 2, Pp 82-85 (2021)
Objective:. Isolated hereditary hypotrichosis is caused by mutations in as many as 11 different genes. The conventional mutation detection strategy consists of sequencing of individual candidate genes separately, a time consuming and costly approach.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51a906b1ed873adcf1be5a19fa4d27b
https://doi.org/10.1097/jd9.0000000000000168
https://doi.org/10.1097/jd9.0000000000000168
Autor:
Pardis Ghazizadeh Tehrani, Mohammad Taheri, Masoume Amini, Mehrdad Hashemi, Maryam Abiri, Razieh Zeinali, Mohammad-Sadegh Fallah, Hossein Farahzadi, Fatemeh Golnabi, Zohreh Sharifi, Hamideh Bagherian, Sadaf Asnavandi, Flora Forouzesh, Sirous Zeinali, Marjan Alborji
Publikováno v:
Journal of Molecular Neuroscience. 71:2281-2298
Spinal muscular atrophies (SMAs) are a heterogeneous group of neuromuscular diseases characterized by loss of motor neurons, muscle weakness, hypotonia and muscle atrophy, with different modes of inheritance; however, the survival motor neuron 1 (SMN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4555c388f4b725a836efb7f9d13af9e8
https://doi.org/10.1007/s12031-020-01789-0
https://doi.org/10.1007/s12031-020-01789-0
Autor:
Maryam Abiri, F. Zafarghandi Motlagh, Sirous Zeinali, Tina Shirzadeh, Z. Salehi, Mohsin M. Jamali, S. Dabbagh, Hamideh Bagherian, Mohammad-Sadegh Fallah, S. Ghasri
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-8 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Glanzmann thrombasthenia (GT) is a rare autosomal recessive abnormality of platelet aggregation with quantitative and/or qualitative abnormality of αIIbβ3 integrin. The αIIbβ3 is a platelet fibrinogen receptor, which is required for pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f833c4536f313022518789b89a2155e3
http://link.springer.com/article/10.1186/s13023-019-1042-4
http://link.springer.com/article/10.1186/s13023-019-1042-4
Autor:
Sarah Azadmehr, Faezeh Rahiminejad, Fatemeh Zafarghandi Motlagh, Mojdeh Jamali, Pardis Ghazizadeh Tehrani, Tina Shirzadeh, Hamideh Bagherian, Morteza Karimipoor, Elham Davoudi-Dehaghani, Sirous Zeinali
Publikováno v:
Archives of Iranian medicine. 24(12)
Background: Hemophilia A (HA) is an X-linked recessive bleeding disorder with a high rate of genetic heterogeneity. The present study was conducted on a large cohort of Iranian HA patients and data obtained from databases. Methods: A total of 622 Ira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e2dbddcd4adc891975585c7f7112c5
https://pubmed.ncbi.nlm.nih.gov/35014236
https://pubmed.ncbi.nlm.nih.gov/35014236