Search Results - "Adnan Issa Al-Badran"

Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene by Neissi, Mostafa, Mohammadi-Asl, Javad, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Sheikh-Hosseini, Motahareh, Issa Al-Badran, Adnan

“…This study delves into Usher syndrome type 2 (USH2), an uncommon genetic disorder characterized by sensorineural hearing loss (HL) and retinitis pigmentosa…”
Get full text

Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9 by Neissi, Mostafa, Sheikh‐Hosseini, Motahareh, Mohammadi‐Asl, Misagh, Al‐Badran, Adnan Issa, Roghani, Mojdeh, Mohammadi‐Asl, Javad, Jorfi, Kamele

“…Key Clinical Message The discovery of compound heterozygous NMNAT1 mutations (c.245T>C; p.Val82Ala and c.575A>G; p.Asp192Gly) provides a genetic explanation…”
Get full text

Mutational spectrum of the AP3B1 gene in an Iraqi family affected with Hermansky-Pudlak syndrome type 2 by Neissi, Mostafa, Al-Badran, Adnan Issa

“…Background Hermansky-Pudlak syndrome type 2 (HPS2) is a rare autosomal recessive inherited disease present with partial oculocutaneous albinism, nystagmus,…”
Get full text

Homozygous AHI1 gene mutation (c.1213A>C; Thr405Pro) leads to Joubert syndrome in a consanguineous Iranian family: A case report by Neissi, Mostafa, Issa Al-Badran, Adnan, Mohammadi-Asl, Javad

“…Joubert syndrome (JS) is an autosomal recessive (AR) neurological disorder primarily characterized by aplasia/hypoplasia of the cerebellar vermis, retinal…”
Get full text

Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report by Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Javad

“…Background Leber congenital amaurosis (LCA), the severe form of inherited retinal degenerative disorder, is a prevalent disorder in the first year of life…”
Get full text

Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis by Neissi, Mostafa, Misagh Mohammadi-Asl, Mojdeh Roghani, Issa Al-Badran, Adnan, Motahareh Sheikh-Hosseini, Mohammadi-Asl, Javad

“…Joubert syndrome (JS), a rare neurodevelopmental disorder, is characterized by a unique midbrain- hindbrain malformation known as the molar tooth sign, a…”
Get full text

A Novel SLC9A6 Mutation Associated with Christianson Syndrome in a Non-Consanguineous Iranian Family: A Case Report by Mehdi Hashemipour, Mostafa Neissi, Mahsa Rashid, Karim Sevari, Motahareh Sheikh-Hosseini, Adnan Issa Al-Badran

“…Introduction: Christianson syndrome is a neurological disorder characterized by recurrent seizures resulting from abnormal brain neuron discharge. Primarily…”
Get full text

A novel missense mutation in PLEKHG5 gene causing an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease in an Iraqi family by Neissi, Mostafa, Mabudi, Hadideh, Al-Badran, Adnan Issa, Mohammadi-Asl, Javad, Al-Badran, Raed Abdulelah

“…Background Charcot-Marie-Tooth disease comprises a large spectrum of clinically heterogeneous disorders. PLEKHG5 variants have shown an intermediate form of…”
Get full text

A novel heterozygous TPM2 gene mutation in an Iranian family affected by distal arthrogryposis type 1: a case report by Neissi, Mostafa, Sheikh-Hosseini, Motahareh, Mohammadi-Asl, Javad, Al-Badran, Adnan Issa

“…Background Distal arthrogryposis (DA) is a group of clinically and genetically heterogeneous disorders characterized by congenital contractures of the distal…”
Get full text

Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant by Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Misagh, Al-Badran, Raed Abdulelah, Sheikh-Hosseini, Motahareh, Roghani, Mojdeh, Mohammadi-Asl, Javad

“…Background Niemann-Pick disease type C poses a significant challenge within the landscape of rare genetic disorders, marked by its connection to variants in…”
Get full text

Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss by Mostafa Neissi, Mostafa Neissi, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Al-Badran, Adnan, Mohammadi-Asl, Javad

“…Hearing loss, recognized as one of the most prevalent sensory disorders, encompasses both syndromic and non-syndromic manifestations, with the identification…”
Get full text

Detection of an FYCO1 nonsense mutation in an affected patient with autosomal recessive cataract : a case report by Al-Badran, Raed Abdulelah, Al-Badran, Adnan Issa, Mabudi, Hadideh, Neissi, Mostafa, Mohammadi-Asl, Javad

“…Background Autosomal recessive cataract (CTRCT18) is a rare type of congenital cataract that develops to complete and lifelong childhood blindness. This…”
Get full text

Hormone receptor-related gene polymorphisms and prostate cancer risk in North Indian population by Onsory, Khadijeh, Sobti, R. C, Al-Badran, Adnan Issa, Watanabe, Masatoshi, Shiraishi, Taizo, Krishan, Awtar, Mohan, Harsh, Kaur, Pushpinder

“…The purpose of this study was to analyse the frequency and type of mutations in the coding region of androgen receptor (AR) and to determine the role of…”
Get full text

Mitochondrial DNA (hypervariable region I) diversity in Basrah population – Iraq by Ohied, Bassim Muften, Al-Badran, Adnan Issa

“…In attempt to investigate the origin of Basrah, we examined the mitochondrial DNA(mt-DNA) variations by hypervariable segment 1(HVS1) Sequencing and…”
Get full text

Y-chromosome variation in Basrah population by Ohied, Bassim Muften, Al-Badran, Adnan Issa

“…Y-chromosome DNA profiles are promising tools in population genetics and forensic science. Analysis of Y-chromosome variety was performed on a total of 191…”
Get full text

PSCA gene expression in bladder, colorectal and prostate cancer patients from Basrah governorate southern of Iraq by Ayoob, Anwar Noori, Al-Badran, Adnan Issa, Abood, Rafid Adil

“…Cancer causes death in all countries of the world, with approximately (9.6) million deaths in 2018. Developing countries have high cancer rates. Furthermore,…”
Get full text

A study of the relationship between the Galectin-9 gene (LGALS9) in three types of cancer patients in Basrah, Iraq by Ayoob, Anwar N., Al-Badran, Adnan Issa, Abood, Rafid A.

“…Background. One essential member of the galectin family, galactose lectin-9 (Gal-9) serves several functions as a multi-subtype lectin. According to the latest…”
Get full text

Profile of Interleukin-6 and Tumor Necrosis Factor-α in Hospitalized COVID-19 Patients by Saeed, Khlood Noori, Shnawa, Bushra Hussain, Al-Badran, Adnan Issa

“…Abstract Background: In 2019’s December, the new COVID-19 coronavirus induced severe lower respiratory tract syndrome in Wuhan, China. Severe acute respiratory…”
Get full text

Preparation of Poly (methyl methacrylate) thin film Capacitors on ITO-glass substrate by S. Ali, Ali, M. Zaidan, Karema, Issa Al-Badran, Adnan

“…In electronic devices, some important materials having a high dielectric constant can be used. Polymer-ceramic composites have a high dielectric constant and…”
Get full text

Genetic susceptibility of Iraqis for obesity and type 2 diabetes: LEPR gene polymorphisms by Almyah, Maysoon K., Al-Badran, Adnan Issa

Get full text