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Molecular and Cellular Biology|July 30, 2008
The 9-1-1 DNA clamp is required for immunoglobulin gene conversionAlihossein Saberi, Makoto Nakahara, Julian E Sale, et al.
Molecular Genetics & Genomic Medicine|December 29, 2022
Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from IranAtefe Papi, Mina Zamani, Gholamreza Shariati, et al.
International Journal of Preventive Medicine|October 22, 2020
Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome SequencingSamira Negahdari, Mina Zamani, Tahereh Seifi, et al.
Frontiers in Genetics|March 1, 2024
Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian familiesRezvan Zabihi, Mina Zamani, Majid Aminzadeh, et al.
The EMBO Journal|February 25, 2006
Parp-1 protects homologous recombination from interference by Ku and Ligase IV in vertebrate cellsHelfrid Hochegger, Donniphat Dejsuphong, Toru Fukushima, et al.
Nature Structural & Molecular Biology|October 22, 2008
FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathwayMasamichi Ishiai, Hiroyuki Kitao, Agata Smogorzewska, et al.
Iranian Journal of Child Neurology|May 1, 2019
Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic AnalysisSomayyeh Hashemian, Peyman Eshraghi, Nafi Dilaver, et al.
Clinical Genetics|September 15, 2025
Exome Sequencing Reveals Novel Variants in Genetic Skeletal Disorders: Insights From a Cohort in Southwest IranRezvan Zabihi, Mina Zamani, Niloofar Chamanrou, et al.
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