Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Seyed Alireza Dastgheib"'
Autor:
Mohammad Golshan-Tafti, Seyed Alireza Dastgheib, Reza Bahrami, Maryam Yeganegi, Maryam Aghasipour, Zahra Marzbanrad, Maryam Saeida-Ardekani, Amirhossein Shahbazi, Amirhossein Omidi, Mohamad Hosein Lookzadeh, Seyed Reza Mirjalili, Mahmood Noorishadkam, Hossein Neamatzadeh
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Neonatal diabetes mellitus (NDM) is a rare, insulin-dependent diabetes that manifests within the first month of life and requires insulin therapy for management. NDM is categorized into two primary types: transient NDM (TNDM), which typicall
Externí odkaz:
https://doaj.org/article/a714b84c45ef402e8a70cc20c5b4e404
Autor:
Seyed Masoud HaghighiKian, Ahmad Shirinzadeh-Dastgiri, Reza Ershadi, Mohammad Vakili-Ojarood, Maedeh Barahman, Seyed Alireza Dastgheib, Fatemeh Asadian, Amirmasoud Shiri, Maryam Aghasipour, Amirhossein Rahmani, Kazem Aghili, Hossein Neamatzadeh
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Objective This meta-analysis aims to clarify the association between the TNF-α -308G > A and − 238G > A polymorphisms and lung cancer risk. Method A comprehensive search was conducted for relevant articles across databases such as PubMed,
Externí odkaz:
https://doaj.org/article/c144f988d60548eaa89682e5dd1115b0
Autor:
Mohammad Golshan-Tafti, Seyed Alireza Dastgheib, Kamran Alijanpour, Reza Bahrami, Mahta Mazaheri, Hossein Neamatzadeh
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Congenital talipes equinovarus (CTEV) is a prevalent pediatric deformity with a multifactorial etiology. The objective of this meta-analysis was to explore the association between genetic variations in COL9A1 and the susceptibilit
Externí odkaz:
https://doaj.org/article/81ced83cfc584346b906d02a9f387f5d
Autor:
Mohammad Golshan-Tafti, Reza Bahrami, Seyed Alireza Dastgheib, Mohamad Hosein Lookzadeh, Seyed Reza Mirjalili, Maryam Yeganegi, Maryam Aghasipour, Amirmasoud Shiri, Ali Masoudi, Amirhossein Shahbazi, Sepideh Azizi, Mahmood Noorishadkam, Hossein Neamatzadeh
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectivePrevious studies on the link between VEGF gene polymorphisms and bronchopulmonary dysplasia (BPD) have yielded inconsistent results. This meta-analysis sought to clarify the relationship between genetic variations in the VEGF gene and the ri
Externí odkaz:
https://doaj.org/article/172bf2bf35bc48b5b956e197745d3672
Autor:
Mahsa Danaie, Maryam Yeganegi, Seyed Alireza Dastgheib, Reza Bahrami, Fatemeh Jayervand, Amirhossein Rahmani, Maryam Aghasipour, Mohammad Golshan-Tafti, Sepideh Azizi, Zahra Marzbanrad, Ali Masoudi, Amirmasoud Shiri, Mohamad Hosein Lookzadeh, Mahmood Noorishadkam, Hossein Neamatzadeh
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology: X, Vol 23, Iss , Pp 100334- (2024)
Childhood obesity represents a pressing global public health concern due to its widespread prevalence and its close connection to early-life exposure to risk factors. The onset of obesity is contingent upon the interplay of genetic composition, lifes
Externí odkaz:
https://doaj.org/article/752211b677324bef87d7677ea30fb2d5
Autor:
Zahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Mehdi Dianatpour, Seyed Alireza Dastgheib
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-4 (2023)
Abstract Pathogenic variants in the EPS8 gene result in nonsyndromic hearing loss. This gene encodes the EPS8 protein in cochlear inner hair cells and performs critical roles in stimulating actin polymerization and bundling. Thus far, only four patho
Externí odkaz:
https://doaj.org/article/6ca95923618a49b39336cf87969a1600
Autor:
Mohammadali Jafari, Seyed Alireza Dastgheib, Farzad Ferdosian, Hamid Mirjalili, Hossein Aarafi, Mahmood Noorishadkam, Mahta Mazaheri, Hossein Neamatzadeh
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 2, Pp 225-234 (2022)
Introduction: The coronavirus disease-2019 (COVID-19) has emerged as a novel infection which has spread rapidly across the globe and currently presents a grave threat to the health of the cancer patient. Objective: The aim of this meta-analysis was t
Externí odkaz:
https://doaj.org/article/7064032a23d4404896a7ded82993ca01
Autor:
Omid Alavi, Hossein Jafari Khamirani, Sina Zoghi, Afrooz Feili, Seyed Alireza Dastgheib, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Seyed Mehdi Panahandeh, Majid Kamali, Mehdi Dianatpour
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Abstract In this study, we detected a novel pathogenic variant and a previously reported variant in RAB3GAP1 by whole-exome sequencing (NM_001172435.2: c.1552C>T, p.Gln518*; c.1471C>T, p.Arg491*). The first patient is a 3-year-old girl who presented
Externí odkaz:
https://doaj.org/article/869143df30c6493b988834f5783b98e8
Autor:
Hossein Jafari Khamirani, Vivek Reddy Palicharla, Seyed Alireza Dastgheib, Mehdi Dianatpour, Mohammad Hadi Imanieh, Seyed Sajjad Tabei, Whitney Besse, Saikat Mukhopadhyay, Karel F. Liem
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Patient variants in Tubby Like Protein-3 (TULP3) have recently been associated with progressive fibrocystic disease in tissues and organs. TULP3 is a ciliary trafficking protein that links membrane-associated proteins to the intraflagellar transport
Externí odkaz:
https://doaj.org/article/4157e2281f3549b5a19d779018310032
Autor:
Jamal Manoochehri, Seyed Alireza Dastgheib, Hossein Jafari Khamirani, Maryam Mollaie, Zahra Sharifi, Sina Zoghi, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Fatemeh Dehghanian, Zahra Farbod, Mehdi Dianatpour
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Abstract GM3 synthase deficiency is associated with salt and pepper developmental regression syndrome (SPDRS), a rare genetic disorder. Herein, we report the first Iranian patient with SPDRS. We detected a novel pathogenic variant of ST3GAL5 (NM_0038
Externí odkaz:
https://doaj.org/article/0ddf93c5e389419abf769016b5259ae2