Seyed Alireza Dastgheib

A comprehensive overview of genetic mutations in Iranian patients with Bardet-Biedl syndrome

Sheyda Khalilian, Mohadeseh Fathi, Mona Entezam, Zahra Farbood et autres

ir (code pays fourni par la source)

The Expression of Long Noncoding RNA FOXD2-AS1 and OIP5-AS1 in Breast Cancer and Its Relationship with Clinicopathological Characteristics

Mahboubeh Khodaparast, Seyed Alireza Dastgheib, Yaser Mansoori, Hamed Goodarzi et autres

ir (code pays fourni par la source)

Whole Exome Sequencing Identified a Novel Mutation in the LOXHD1 Gene in Consanguineous Iranian Families With Hearing Loss

Solmaz Hassani Fard Katiraei, Milad Gholami, Mohsen Soosanabadi, Mona Entezam et autres

ir (code pays fourni par la source)

Molecular and clinical heterogeneity in an Iranian case series of Joubert syndrome

Sheyda Khalilian, Mohadeseh Fathi, Zahra Farbood, Fatemeh Dehghanian et autres

ir (code pays fourni par la source)

Association of XPD Gene Polymorphisms with Cutaneous Melanoma Risk: A Meta-Analysis and Trial Sequence Evaluation

Nazila Farnoush, Amirhossein Rahmani, Mehdi Khosravi-Mashizi, Amirmasoud Shiri et autres

Association of XPD Gene Polymorphisms with Cutaneous Melanoma Risk: A Meta-Analysis and Trial Sequence Evaluation

Nazila Farnoush, Amirhossein Rahmani, Mehdi Khosravi-Mashizi, Amirmasoud Shiri et autres

Association of XPD Gene Polymorphisms with Cutaneous Melanoma Risk: A Meta-Analysis and Trial Sequence Evaluation

Nazila Farnoush, Amirhossein Rahmani, Mehdi Khosravi-Mashizi, Amirmasoud Shiri et autres

ir, us (code pays fourni par la source)

Artificial intelligence in ADHD diagnosis: a comprehensive review of machine learning applications, clinical validation challenges, and implementation barriers in precision medicine

Bita Fallahpour, Ghasem Dastjerdi, Elahe Akbarian, Alireza Emarati et autres

ir (code pays fourni par la source)

IL-6 Promoter Polymorphisms and Breast Cancer Susceptibility: A Meta-Analysis of 16,499 Cases and 21,186 Controls

Alireza Negahi, Hossein Negahban, Soheila Sayad, Mehdi Khosravi-Mashizi et autres

ir (code pays fourni par la source)

A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literature

Alireza Ahmadkhani, Erfan Taherifard, Sina Zoghi, Hossein Jafari Khamirani et autres

ir (code pays fourni par la source)

Optimized delivery of dual-gRNA CRISPR/Cas9 via FolicPolySpermine nanoparticles for MHC class I elimination through B2M gene knockout

Hossein Jafari Khamirani, Maryam Aghasipour, Somayeh Khoddam, Amirmasoud Shiri et autres

ir, us (code pays fourni par la source)

Concurrent inheritance of achromatopsia and MMAT syndrome in a pedigree: Genetic and clinical insights

Maryam Aghasipour, Sina Zoghi, Afrooz Feili, Hossein Jafari Khamirani et autres

us, ir (code pays fourni par la source)