Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Amin Hosseini Nami"'
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:
Vahid Hosseini, Simone Schuerle, Thomas M. Valentin, Daphne O. Asgeirsson, Amin Hosseini Nami, Luca Somm, Nima Mirkhani, Michael G. Christiansen
Publikováno v:
Lab on a Chip, 21 (20)
Lab on a Chip
Lab on a Chip
Cells continuously sense and react to mechanical cues from their surrounding matrix, which consists of a fibrous network of biopolymers that influences their fate and behavior. Several powerful methods employing magnetic control have been developed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::666baf8b5d7c03f8493cb716a3791c9b
https://doi.org/10.1039/d1lc00657f
https://doi.org/10.1039/d1lc00657f
Publikováno v:
Iranian biomedical journal. 26(5)
Cystic fibrosis (CF) is the most common heredity disease among the Caucasian population. More than 350 known pathogenic variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene (NM_000492.4) cause CF. Herein, we report the ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c72a69492b60915b7f15e90e5b077eb
https://pubmed.ncbi.nlm.nih.gov/35468710
https://pubmed.ncbi.nlm.nih.gov/35468710
Autor:
Sayed-Amir, Marashi, Seyed Mohammad Amin, Hosseini-Nami, Khadijeh, Alishah, Mahdieh, Hadi, Ali, Karimi, Saeedeh, Hosseinian, Rouhallah Ramezani, Fard, Reihaneh Sadat, Mirhassani, Zhaleh, Hosseini, Zahra, Shojaie
Publikováno v:
EXCLI Journal
It has been suggested that the “visibility” of an article influences its citation count. More specifically, it is believed that the social media can influence article citations.Here we tested the hypothesis that inclusion of scholarly references
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e74b1404bad6a3430df2b1d5f991325
https://pubmed.ncbi.nlm.nih.gov/27034629
https://pubmed.ncbi.nlm.nih.gov/27034629