Search Results - "Mojarrad, Majid"

AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data by Quinodoz, Mathieu, Peter, Virginie G, Bedoni, Nicola, Royer Bertrand, Béryl, Cisarova, Katarina, Salmaninejad, Arash, Sepahi, Neda, Rodrigues, Raquel, Piran, Mehran, Mojarrad, Majid, Pasdar, Alireza, Ghanbari Asad, Ali, Fonseca Vieira Álvares Sousa Ferrand Almeida, Ana Berta, Santos, Maria Luisa, Superti-Furga, Andrea, Rivolta, Carlo

“…© The Author(s) 2021. Open AccessThis article is licensed under a Creative CommonsAttribution 4.0 International License, which permits use, sharing,adaptation,…”
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Long non-coding RNAs as the critical factors during tumor progressions among Iranian population: an overview by Rahmani, Zahra, Mojarrad, Majid, Moghbeli, Meysam

“…Cancer is associated with various genetic and environmental risk factors. Beside the mutations or aberrant expression of protein-coding genes, the genetic…”
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Non coding RNAs as the critical factors in chemo resistance of bladder tumor cells by Zangouei, Amir Sadra, Rahimi, Hamid Reza, Mojarrad, Majid, Moghbeli, Meysam

“…Bladder cancer (BCa) is the ninth frequent and 13th leading cause of cancer related deaths in the world which is mainly observed among men. There is a…”
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Genetic and molecular biology of bladder cancer among Iranian patients by Mojarrad, Majid, Moghbeli, Meysam

“…Background Bladder cancer (BC) is the sixth common cancer among Iranians. Various risk factors such as smoking, body mass index, chronic infection, age, and…”
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Role of tyrosine kinases in bladder cancer progression: an overview by Zangouei, Amir Sadra, Barjasteh, Amir Hossein, Rahimi, Hamid Reza, Mojarrad, Majid, Moghbeli, Meysam

“…Bladder cancer (BCa) is a frequent urothelial malignancy with a high ratio of morbidity and mortality. Various genetic and environmental factors are involved…”
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Role of microRNAs in regulation of WNT signaling pathway in urothelial and prostate cancers by Montazer, Mehdi, Taghehchian, Negin, Mojarrad, Majid, Moghbeli, Meysam

“…Background Urothelial cancer (UC) and prostate cancer (PCa) are the most common cancers among men with a high ratio of mortality in advanced-stages. The higher…”
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Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies by Rehman, Atta Ur, Sepahi, Neda, Bedoni, Nicola, Ravesh, Zeinab, Salmaninejad, Arash, Cancellieri, Francesca, Peter, Virginie G., Quinodoz, Mathieu, Mojarrad, Majid, Pasdar, Alireza, Asad, Ali Ghanbari, Ghalamkari, Saman, Piran, Mehran, Piran, Mehrdad, Superti-Furga, Andrea, Rivolta, Carlo

“…Inherited retinal dystrophies (IRDs) constitute one of the most heterogeneous groups of Mendelian human disorders. Using autozygome-guided next-generation…”
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Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies by Salmaninejad, Arash, Bedoni, Nicola, Ravesh, Zeinab, Quinodoz, Mathieu, Shoeibi, Nasser, Mojarrad, Majid, Pasdar, Alireza, Rivolta, Carlo

“…Inherited retinal dystrophies (IRDs), displaying pronounced genetic and clinical heterogeneity, comprise of a broad range of diseases characterized by…”
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Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents by Yan, Denise, Tekin, Demet, Bademci, Guney, Foster, Joseph, Cengiz, F. Basak, Kannan-Sundhari, Abhiraami, Guo, Shengru, Mittal, Rahul, Zou, Bing, Grati, Mhamed, Kabahuma, Rosemary I., Kameswaran, Mohan, Lasisi, Taye J., Adedeji, Waheed A., Lasisi, Akeem O., Menendez, Ibis, Herrera, Marianna, Carranza, Claudia, Maroofian, Reza, Crosby, Andrew H., Bensaid, Mariem, Masmoudi, Saber, Behnam, Mahdiyeh, Mojarrad, Majid, Feng, Yong, Duman, Duygu, Mawla, Alex M., Nord, Alex S., Blanton, Susan H., Liu, Xue Z., Tekin, Mustafa

“…Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific…”
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CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family by Ghouchanatigh, Mahdieh, Khan, Ranjha, Mojarrad, Majid, Hameed, Uzma, Zubair, Muhammad, Waqas, Ahmed, Jalali, Mohsen, Kalantari, Mahmoudreza, Shamsa, Ali, Zhang, Huan, Shi, Qing-Hua

“…Cystic fibrosis (CF) is one of the most common recessive genetic diseases, with a wide spectrum of phenotypes, ranging from infertility to severe pulmonary…”
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Common therapeutic advances for Duchenne muscular dystrophy (DMD) by Salmaninejad, Arash, Jafari Abarghan, Yousef, Bozorg Qomi, Saeed, Bayat, Hadi, Yousefi, Meysam, Azhdari, Sara, Talebi, Samaneh, Mojarrad, Majid

“…Background and purpose: Duchenne muscular dystrophy (DMD), a lethal X-linked recessive muscle dystrophy, is resulted in by different mutations including mostly…”
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Role of extra cellular proteins in gastric cancer progression and metastasis : an update by Abbaszadegan, Mohammad Reza, Mojarrad, Majid, Moghbeli, Meysam

“…[Abstract] [Background :] Gastric cancer (GC) is one of the most common cancers in the world with a high ratio of mortality. Regarding the late diagnosis,…”
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Genetic and molecular biology of gastric cancer among Iranian patients: an update by Abbaszadegan, Mohammad Reza, Mojarrad, Majid, Rahimi, Hamid Reza, Moghbeli, Meysam

“…Background There is a declining trend of gastric cancer (GC) incidence in the world during recent years that is related to the development of novel diagnostic…”
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MicroRNAs as the critical regulators of protein kinases in prostate and bladder cancers by Zangoue, Malihe, Zangouei, Amir Sadra, Mojarrad, Majid, Moghbeli, Meysam

“…Background Bladder cancer (BCa) and prostate cancer (PCa) are frequent urothelial and genital malignancies with a high ratio of morbidity and mortality which…”
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A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome by Ghosh, Shereen G, Scala, Marcello, Beetz, Christian, Helman, Guy, Stanley, Valentina, Yang, Xiaoxu, Breuss, Martin W, Mazaheri, Neda, Selim, Laila, Hadipour, Fatemeh, Pais, Lynn, Stutterd, Chloe A, Karageorgou, Vasiliki, Begtrup, Amber, Crunk, Amy, Juusola, Jane, Willaert, Rebecca, Flore, Leigh A, Kennelly, Kelly, Spencer, Christopher, Brown, Martha, Trapane, Pamela, Hurst, Anna C E, Lane Rutledge, S, Goodloe, Dana H, McDonald, Marie T, Shashi, Vandana, Schoch, Kelly, Tomoum, Hoda, Zaitoun, Raghda, Hadipour, Zahra, Galehdari, Hamid, Pagnamenta, Alistair T, Mojarrad, Majid, Sedaghat, Alireza, Dias, Patrícia, Quintas, Sofia, Eslahi, Atiyeh, Shariati, Gholamreza, Bauer, Peter, Simons, Cas, Houlden, Henry, Issa, Mahmoud Y, Zaki, Maha S, Maroofian, Reza, Gleeson, Joseph G

“…Trafficking protein particle (TRAPP) complexes, which include the TRAPPC4 protein, regulate membrane trafficking between lipid organelles in a process termed…”
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Genetics of blood malignancies among Iranian population: an overview by Ghayour-Mobarhan, Majid, Zangouei, Amir Sadra, Hosseinirad, Seyed Mohammad, Mojarrad, Majid, Moghbeli, Meysam

“…Blood malignancies are among the leading causes of cancer related deaths in the world. Different environmental and genetic risk factors are involved in…”
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TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia by Mohajeri, Mahsa Sadat Asl, Eslahi, Atieh, Khazaii, Zeinab, Moradi, Mohammad Reza, Pazhoomand, Reza, Farrokhi, Shima, Feizabadi, Masoumeh Heidari, Alizadeh, Farzaneh, Mojarrad, Majid

“…Skeletal dysplasia is a common, clinically and genetically heterogeneous disorder in the human population. An increasing number of different genes are being…”
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Genetic and molecular biology of systemic lupus erythematosus among Iranian patients: an overview by Gachpazan, Meisam, Akhlaghipour, Iman, Rahimi, Hamid Reza, Saburi, Ehsan, Mojarrad, Majid, Abbaszadegan, Mohammad Reza, Moghbeli, Meysam

“…Systemic lupus erythematosus (SLE) is a clinicopathologically heterogeneous chronic autoimmune disorder affecting different organs and tissues. It has been…”
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An Overview of the CRISPR-Based Genomic- and Epigenome-Editing System: Function, Applications, and Challenges by Bozorg Qomi, Saeed, Asghari, Amir, Mojarrad, Majid

“…Developing a new strategy for an efficient targeted genome editing has always been a great perspective in biology. Although different approaches have been…”
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Role of MicroRNAs in Pathophysiology of Non-alcoholic Fatty Liver Disease and Non-alcoholic Steatohepatitis by Iravani, Farzaneh, Hosseini, Neda, Mojarrad, Majid

“…Non-alcoholic fatty liver disease (NAFLD) is the most common liver disorder worldwide. It includes wide range of diseases from different subtypes of simple…”
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