Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Monavvar, Andarva"'
Autor:
Narsis Daftarian, Ramin Pouriran, Javad Jamshidi, Babak Emamalizadeh, Elham Alehabib, Hossein Darvish, Hamid Ghaedi, Shaghyegh Taghavi, Monavvar Andarva
Publikováno v:
Clinical and Experimental Optometry. 101:255-259
Background Norrie disease (ND) is a rare, X-linked recessive disorder with the main characteristic of early childhood blindness. The aim of the present study was to identify the genetic cause of the disease and the phenotypic characteristics of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77d7f41c6ce07062b6626c2bd7fe010
https://doi.org/10.1111/cxo.12599
https://doi.org/10.1111/cxo.12599
Autor:
Shaghyegh Taghavi, Simin Rahimi-Aliabadi, Haleh Akhavan-Niaki, Neda Shahmohammadibeni, Javad Jamshidi, Ramin Pouriran, Farhad Ramezani Nejad, Ehteram Khademi, Parasto Shokraeian, Elham Alehabib, Coro Paisán-Ruiz, Ehsan Esmaili Shandiz, Mina Ohadi, Monavvar Andarva, Nader Mansoori, Azadeh Ahmadifard, Hossein Darvish
Publikováno v:
Genetic Testing and Molecular Biomarkers. 21:485-490
The role of short tandem repeats (STRs) in the control of gene expression among species is being increasingly understood following the identification of several instances in which certain STRs occur identically, or expand differentially, in primates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927af9cfb798cda161819115f2722fc7
https://doi.org/10.1089/gtmb.2016.0422
https://doi.org/10.1089/gtmb.2016.0422
Autor:
Behnam Safarpour Lima, Shaghayegh Taghavi, Monavvar Andarva, Mahmoud Shekari Khaniani, Parasto Shokraeian, Tannaz Safaralizadeh, Peyman Petramfar, Ali Kowsari, Minoo Atakhorrami, Abolfazl Movafagh, Gholam Ali Shahidi, Azadeh Ahmadifard, Tahereh Dadkhah, Mina Ohadi, Marzieh Motallebi, Babak Emamalizadeh, Hossein Darvish, Elham Alehabib, Neda Shahmohammadibeni, Ali Khaligh, Javad Jamshidi, Mohammad Javad Soltani Banavandi, Somayyeh Kazeminasab, Mehdi Khorrami, Ehteram Khademi, Akbar Biglarian, Abbas Tafakhori, Arash Mirabzadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli
Publikováno v:
Molecular Neurobiology. 54:2234-2240
Neurological disorders include a wide variety of mostly multifactorial diseases related to the development, survival, and function of the neuron cells. Single-nucleotide polymorphisms (SNPs) have been extensively studied in neurological disorders, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ea67477b0995804e8ecfd77416a757
https://doi.org/10.1007/s12035-016-9815-4
https://doi.org/10.1007/s12035-016-9815-4
Autor:
Elham, Alehabib, Javad, Jamshidi, Hamid, Ghaedi, Babak, Emamalizadeh, Monavvar, Andarva, Narsis, Daftarian, Mozhgan, Rezaei Kanavi, Peyman, Mohammadi Torbati, Goldis, Espandar, Somayeh, Alinaghi, Amir Hossein, Johari, Mansoor, Saghally, Fatemeh, Mohajerani, Hossein, Darvish
Publikováno v:
International Journal of Molecular and Cellular Medicine
In the current study, we conducted a mutation screening of tumor-associated calcium signal transducer 2 (TACSTD2) gene in six consanguineous Iranian families with gelatinous drop-like corneal dystrophy (GDLD), in order to find the causative mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54e695d5f938898eba4581892dd0604b
https://pubmed.ncbi.nlm.nih.gov/29988226
https://pubmed.ncbi.nlm.nih.gov/29988226
Autor:
Peyman Petramfar, Arman Habibi, Faranak Madadi, Zahra Taherian-Esfahani, Hossein Ehsanbakhsh, Banafsheh Mohammad Hossein Pour, Marzieh Motallebi, Saeed Askarpour, Shiva Askarpour, Monavvar Andarva, Mona Ahmadi, Mahdis Bayat, Mehdi Khorrami, Luis J. Azcona, Hajar Eftekhari, Zahra Azimzadeh, Reza Ebrahimi Rad, Jalal Rezaeidian, Gholam Ali Shahidi, Azadeh Ahmadifard, Safa Najmi, Javad Jamshidi, Seyed Erfan Mortazavi, Rita Chaouni, Ahmad Chitsaz, Zahra Dehghani-Tafti, Hossein Darvish, Elham Alehabib, Faraz Mohammadi, Samareh Omidvari, Abbas Tafakhori, Amir Mohammad Besharati, Seyed Amir Hassan Habibi, Minoo Atakhorrami, Saghar Ghasemi Firouzabadi, Mir Davood Omrani, Babak Emamalizadeh, Hossein Ali Shahmohammadibeni, Coro Paisán-Ruiz, Saeed Mohammadihosseinabad, Parasto Shokraeian, Ehsan Esmaili Shandiz, Shaghayegh Taghavi, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Hamid Noorollahi Moghaddam, Mohammad Ali Harati-Ghavi
Publikováno v:
Molecular neurobiology. 55(4)
In this study, the role of known Parkinson’s disease (PD) genes was examined in families with autosomal recessive (AR) parkinsonism to assist with the differential diagnosis of PD. Some families without mutations in known genes were also subject to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::819e7d2c518a5ea5ad689dd00a5d651b
https://pubmed.ncbi.nlm.nih.gov/28502045
https://pubmed.ncbi.nlm.nih.gov/28502045
Autor:
Mina Ohadi, Monavvar Andarva, Hossein Darvish, Babak Emamalizadeh, Somayeh Kazeminasab, Pegah Namdar-Aligoodarzi, Abofazl Movafagh
Publikováno v:
Molecular genetics and genomics : MGG. 292(3)
Evolutionary analyses of the critical core promoter interval support a selective advantage for expanding the length of certain short tandem repeats (STRs) in humans. We recently reported genome-wide data on human core promoter STRs that are "exceptio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f708f59e67682a19b1102922e2456365
https://pubmed.ncbi.nlm.nih.gov/28214997
https://pubmed.ncbi.nlm.nih.gov/28214997
Autor:
Azadeh Ahmadifard, Hossein Darvish, Monavvar Andarva, Babak Emamalizadeh, Elham Alehabib, Hamid Ahmadieh, Abbas Tafakhori, Hamid Ghaedi, Simin Rahimi-Aliabadi, Parasto Shokraeian, Rezvan Noroozi, Javad Jamshidi, Shaghyegh Taghavi, Narsis Daftarian, Minoo Atakhorrami
Publikováno v:
Eye (London, England). 30(11)
PurposeJalili syndrome is an autosomal recessive disorder characterized by simultaneous appearance of cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI). Mutations in CNNM4 gene have been identified as the underlying cause of the syndrome. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a2c7b6da3bb6818e2155dbf3edde7f6
https://pubmed.ncbi.nlm.nih.gov/27419834
https://pubmed.ncbi.nlm.nih.gov/27419834
Autor:
Hamid Ghaedi, Mehdi Khorrami, Monavvar Andarva, Babak Emamalizadeh, Narsis Daftarian, Elham Alehabib, Shaghayegh Taghavi, Farhad Assarzadegan, Omid Hesami, Minoo Atakhorrami, Javad Jamshidi, Azadeh Ahmadifard, Behnam Safarpour Lima, Neda Shahmohammadibeni, Hossein Darvish, Nasim Sohrabifar, Rezvan Noroozi, Simin Rahimi-Aliabadi, Hamid Ahmadieh
Publikováno v:
European journal of medical genetics. 59(2)
Wolfram syndrome is one of the rare autosomal recessive, progressive, neurodegenerative disorders, characterized by diabetes mellitus and optic atrophy. Several other features are observed in patients including deafness, ataxia, and peripheral neurop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc9d7db39ac1b8f5347fc2bc12441a12
https://pubmed.ncbi.nlm.nih.gov/26773575
https://pubmed.ncbi.nlm.nih.gov/26773575
Autor:
Mahnoosh Rahimi, Mahnaz Shahmohammadibeni, Hossein Ali Shahmohammadibeni, Monavvar Andarva, Javad Jamshidi, Hajar Eftekhari, Haleh Akhavan-Niaki, Babak Emamalizadeh, Mahmoud Shekari Khaniani, Azadeh Ahmadifard, Ehteram Khademi, Shaghayegh Taghavi, Alireza Zare Bidoki, Hossein Darvish, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Abbas Tafakhori, Atena Fazeli, Minoo Atakhorrami, Marzieh Motallebi, Tahereh Dadkhah, Elham Alehabib, Simin Rahimi-Aliabadi, Shokoufeh Abdollahi
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 37(5)
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder. Both genetic and environmental factors are involved in the etiology of the disease. Many studies have revealed the susceptibility genes and variations for PD which need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560834c8f76d74818e75ae469d17a41e
https://pubmed.ncbi.nlm.nih.gov/26732583
https://pubmed.ncbi.nlm.nih.gov/26732583
Autor:
Simin Rahimi-Aliabadi, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Neda Shahmohammadibeni, Monavvar Andarva, Mina Ohadi, Fatemeh Gholipour, Elham Moslemi, Minoo Atakhorrami, Saeed Mohammadihosseinabad, Abolfazl Movafagh, Shaghayegh Taghavi, Hamid Ghaedi, Faranak Madadi, Marzieh Motallebi, Arash Mirabzadeh, Javad Jamshidi, Babak Emamalizadeh, Azadeh Ahmadifard, Hossein Darvish
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 123(3)
A recent large-scale study have reported that rs1063843, a single nucleotide polymorphism located in the CAMKK2 gene is highly associated with schizophrenia in European and Han Chinese populations. Increasing evidences show that schizophrenia and bip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b20a61d19ecd82d75dbe41af27307c
https://pubmed.ncbi.nlm.nih.gov/26354101
https://pubmed.ncbi.nlm.nih.gov/26354101