Accès ouvert
2026
article
OpenAlex
Anya Omed, Rozhgar A. Khailany
Purpose: This study aims to evaluate the expression patterns of miR-101-3p and its target ADAM15 in colorectal cancer patients. Materials and Methods: Thirty patients with colorectal cancer had their tumor and corresponding normal tissue samples taken. Following RNA extraction, real-time PCR (qRT-PCR) …
iq
(code pays fourni par la source)
2025
article
OpenAlex
Muqdad M. N. Al‐Mousawi, Saad S. Merza, Rozhgar A. Khailany, Ali Abdulghani Ramadhan et autres
All data of relevance to the case has been presented in the manuscript.
iq
(code pays fourni par la source)
2025
article
OpenAlex
Tara Jamel Osman, Rozhgar A. Khailany, Luqman Khalid Rasool, Nasir A.S. Al-Allawi
Dominant β-thalassemia is a rare form of thalassemia that is caused by a heterogenous group of molecular defects, including missense, nonsense, and frameshift mutations. Among the missense mutations involving the third exon of β-globin gene is the rare Hb Dieppe (HBB:c. 383A …
iq
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Rawand Shamoon, Amir Charkaneh, Elena Di Pierro, Milena Agata Irrera et autres
Background Thalassemias are genetic disorders of globin chain synthesis. In Iraq, β-thalassemia is more prevalent than α-thalassemia. This study identifies two unpredicted globin gene mutations, a rare α-globin gene mutation (Hb SKMC) and a novel γδβ-thalassemia deletion.Methods Over 2 years, the Genetics …
iq, it
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Yuji Nakamura, Issei S. Shimada, Reza Maroofian, Micol Falabella et autres
Patatin-like phospholipase domain-containing lipase 8 (PNPLA8), one of the calcium-independent phospholipase A2 enzymes, is involved in various physiological processes through the maintenance of membrane phospholipids. Biallelic variants in PNPLA8 have been associated with a range of paediatric neurodegenerative disorders. However, the phenotypic …
jp, gb, Égypte, ir, de, sa, fr, us, iq, tr, pk
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Qaraman M.K. Koyee, Rozhgar A. Khailany, Mahmud Luqman Rahman, Liza Numan Nassraldin
داء حلزون كبد الاغنام (المتورقات) الناجم عن Fasciola (F.) hepatica وF. gigantica مرض معد يصيب الإنسان والحيوانات المجترة في العديد من دول العالم، بما في ذلك العراق. إن دراسة هذه الطفيليات، وتأثيراتها الضارة على مختلف المضائف، شكليًا ، نسيجيا ، وبائيًا وجزيئيًا …
iq
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Harmand Ali Hama, Bestoon S. Hasan, Basak T. Barzngy, Saman S. Abdulla et autres
Colorectal cancer (CRC) is the third leading cause of cancer-related deaths worldwide. The tumor suppressor gene MT-CO1, and Kristen Rat Sarcoma Virus (KRAS), an oncogene are primarily responsible for controlling cell apoptosis, cell cycle arrest, and cell proliferation, and any irregularities in …
iq, pl
(code pays fourni par la source)
Accès ouvert
2023
preprint
OpenAlex
Yuji Nakamura, Issei S. Shimada, Reza Maroofian, Henry Houlden et autres
Abstract PNPLA8, one of the calcium-independent phospholipase A2 enzymes, is involved in various physiological processes through the maintenance of membrane phospholipids. However, little is known about its role in brain development. Here, we report 12 individuals from 10 unrelated families with biallelic …
jp, gb, ir, de, sa, fr, Égypte, us, iq, tr
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Belan O. Kanabe, Mehmet Özaslan, Sherwan Ahmed Aziz, Mustafa S. Al-Attar et autres
Early diagnosis of breast cancer can increase the survivability of the patients and the patient's quality of life. There is growing evidence demonstrating the active role of LncRNA-GAS5 and miR-103 in cancer biology. APOBEC enzymes are important players in immunity and may …
tr, iq
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Rozhgar A. Khailany, Mehmet Özaslan
Breast cancer is the most common cancer in women worldwide. Detection of breast cancer susceptibility genes is an important issue. Also, MLH3 is a DNA mismatch repair gene and mutation in this gene is harmful in different cancers. This study aimed to …
tr
(code pays fourni par la source)
2021
article
OpenAlex
Sulav D. Atroshi, Nasir A.S. Al-Allawi, David H.K. Chui, Hossein Najmabadi et autres
We report a novel frameshift β-thalassemia (β-thal) mutation due to a two-nucleotide deletion at codon 118 of the β-globin gene (HBB: c.356_357delTT) in a 4-year-old Iraqi Kurd female presenting as transfusion-dependent β-thal. This frameshift mutation, unlike many others involving the third exon, …
iq, us, ir
(code pays fourni par la source)
2020
article
OpenAlex
Sana Zaheer, Rozhgar A. Khailany, Sadaf Parvez, Muhammad Naveed et autres
tr, pk, iq, cn
(code pays fourni par la source)