Inhibition of breast cancer cell growth and migration through siRNA-mediated modulation of circ_0009910/miR-145-5p/MUC1 axis

Autor: Maryam Abtin, Nahid Nafisi, Asghar Hosseinzadeh, Sepideh Kadkhoda, Ramesh Omranipour, Leyla Sahebi, Masoumeh Razipour, Soudeh Ghafouri-Fard, Abbas Shakoori

Publikováno v: Non-coding RNA Research, Vol 9, Iss 2, Pp 367-375 (2024)

Circular RNAs (circRNAs) characterize a novel kind of regulatory RNAs distinguished by great evolutionary conservation and constancy. Although their exact role in malignancies is not fully understood, they mainly work through specific axes. Circular

Externí odkaz: https://doaj.org/article/0c8ba7fb37e247c7a34dad53b7e3212f

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria

Autor: Saeed Talebi, Mona Entezam, Neda Mohajer, Golnaz-Ensieh Kazemi-sefat, Masoumeh Razipour, Somayeh Ahmadloo, Aria Setoodeh, Mohammad Keramatipour

Publikováno v: Cell Journal, Vol 18, Iss 2, Pp 229-236 (2016)

Objective The phenylalanine hydroxylase (PAH) locus has high linkage disequilibrium. Haplotypes related to this locus may thus be considered sufficiently informative for genetic diagnosis and carrier screening using multi-allelic markers. In this

Externí odkaz: https://doaj.org/article/03546ab4cd044946880c921e9ff48ca9

Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report

Autor: Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR

Publikováno v: Iranian Journal of Public Health, Vol 46, Iss 4 (2017)

Phenylketonuria (PKU) is an inborn error of amino acid metabolism with an autosomal recessive inheritance caused in most cases by mutations in the phenylalanine hydroxylase (PAH) gene. PKU has wide allelic heterogeneity. Here we report a novel hetero

Externí odkaz: https://doaj.org/article/1ac23fb6da4d43d3b79a4b0f179855cf

Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree

Autor: Masoumeh Razipour, Mohammad Keramatipour, M Movasat, Daniz Kooshavar

Publikováno v: International Journal of Pediatric Otorhinolaryngology. 104:10-13

Background Usher syndrome (USH) is characterized by congenital hearing loss and retinitis pigmentosa (RP) with a later onset. It is an autosomal recessive trait with clinical and genetic heterogeneity which makes the molecular diagnosis much difficul

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81024fa2aa469640651ba90b3e1ae001
https://doi.org/10.1016/j.ijporl.2017.10.022

Identification of a novel mutation in the ST14 gene in an Iranian family with ichthyosis and hypotrichosis

Autor: Fateme Zahedi Abghari, Maryam Taghavi-Basmenj, Masoumeh Razipour, Morteza Karimipoor, Elham Davoudi-Dehaghani, Maryam Nasimi

Publikováno v: Taghavi-Basmenj, Maryam; Razipour, Masoumeh; Davoudi-Dehaghani, Elham; Nasimi, Maryam; Abghari, Fateme Zahedi; & Karimipoor, Morteza. (2019). Identification of a novel mutation in the ST14 gene in an Iranian family with ichthyosis and hypotrichosis. Dermatology Online Journal, 25(3). Retrieved from: http://www.escholarship.org/uc/item/97m2t21k

Inherited ichthyosis is a heterogeneous group of rare cutaneous disorders characterized by hyperkeratosis and scaly skin. So far, only a few genetic studies on ichthyosis have been performed in Iran. Herein, we reported a family with two cases of ich

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3741d5b8a616eb1cb4e9297f744a4915
http://www.escholarship.org/uc/item/97m2t21k