Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families

Authors: Becker, Aurélie, Felici, Charlotte, Lambert, Laëtitia, Saint Martin, Anne, Abi‐Warde, Marie‐Thérèse, Schaefer, Elise, Zix, Christian, Zamani, Mina, Sadeghian, Saeid, Zeighami, Jawaher, Seifi, Tahereh, Azizimalamiri, Reza, Shariati, Gholamreza, Galehdari, Hamid, Selig, Mareike, Ding, Can, Duerinckx, Sarah, Pirson, Isabelle, Abramowicz, Marc, Clément, Guillemette, Leheup, Bruno, Jonveaux, Philippe, Lefort, Geneviève, Bronner, Myriam, Renaud, Mathilde, Bonnet, Céline

Source: Clinical genetics. 103(3):346-351

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Phenotypic continuum of NFU1‐related disorders

Authors: Kaiyrzhanov, Rauan, Zaki, Maha S., Lau, Tracy, Sen, Sambuddha, Azizimalamiri, Reza, Zamani, Mina, Sayin, Gözde Yeşil, Hilander, Taru, Efthymiou, Stephanie, Chelban, Viorica, Brown, Ruth, Thompson, Kyle, Scarano, Maria Irene, Ganesh, Jaya, Koneev, Kairgali, Gülaçar, Ismail Musab, Person, Richard, Sadykova, Dinara, Maidyrov, Yerdan, Seifi, Tahereh, Zadagali, Aizhan, Bernard, Geneviève, Allis, Katrina, Elloumi, Houda Zghal, Lindy, Amanda, Taghiabadi, Ehsan, Verma, Sumit, Logan, Rachel, Kirmse, Brian, Bai, Renkui, Khalaf, Shaimaa M., Abdel‐Hamid, Mohamed S., Sedaghat, Alireza, Shariati, Gholamreza, Issa, Mahmoud, Zeighami, Jawaher, Elbendary, Hasnaa M., Brown, Garry, Taylor, Robert W., Galehdari, Hamid, Gleeson, Joseph J., Carroll, Christopher J., Cowan, James A., Moreno‐De‐Luca, Andres, Houlden, Henry, Maroofian, Reza

Source: Annals of clinical and translational neurology. 9(12):2025-2035

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100168193948.0x000001&indx=1&recIds=ETOCvdc_100168193948.0x000001

The influence of mechanochemical treatment in hexane on dispersibility and floatability of graphite flakes with enhanced water evaporation performance

Authors: Seifi, Tahereh, Kamali, Ali Reza

Source: In Colloids and Surfaces A: Physicochemical and Engineering Aspects 5 April 2022 638

Antiviral performance of graphene-based materials with emphasis on COVID-19: A review

Authors: Seifi, Tahereh, Reza Kamali, Ali

Source: In Medicine in Drug Discovery September 2021 11

Anti-pathogenic activity of graphene nanomaterials: A review

Authors: Seifi, Tahereh, Kamali, Ali Reza ^*

Source: In Colloids and Surfaces B: Biointerfaces March 2021 199

Whole-Exome Sequencing Application for Genetic Diagnosis of Kidney Diseases: A Study from Southwest of Iran

Authors: Zamani, Mina, Seifi, Tahereh, Sedighzadeh, Sahar, Negahdari, Samira, Zeighami, Jawaher, Sedaghat, Alireza, Yadegari, Tahereh, Saberi, Alihossein, Hamid, Mohammad, Shariati, Gholamreza, Galehdari, Hamid

Source: Kidney360. 2(5):873-877

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100193169972.0x000001&indx=1&recIds=ETOCvdc_100193169972.0x000001

Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy

Authors: Jones, Edward, Mazaheri, Neda, Maroofian, Reza, Zamani, Mina, Seifi, Tahereh, Sedaghat, Alireza, Shariati, Gholamreza, Jamshidi, Yalda, Allen, Hugh, Wehrens, Xander, Galehdari, Hamid, Landstrom, Andrew

Source: Scientific reports. 9(1):1-10

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100181233388.0x000001&indx=1&recIds=ETOCvdc_100181233388.0x000001

3D-graphene nanosheets as efficient antibacterial agent

Authors: Seifi, Tahereh, Kamali, Ali Reza

Source: MATERIALS LETTERS. 321

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100163848749.0x000001&indx=1&recIds=ETOCvdc_100163848749.0x000001

Enhanced dispersion and antibacterial activity of mechanically exfoliated graphite flakes in the presence of n-hexane and NaCl

Authors: Seifi, Tahereh, Kamali, Ali Reza

Source: MATERIALS LETTERS. 304

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100138941949.0x000001&indx=1&recIds=ETOCvdc_100138941949.0x000001

Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran.

Authors: Zamani, Mina^1,2, Sedighzadeh, Sahar^1,2, Seifi, Tahereh^1,2, Negahdari, Samira^2,3, Zeighami, Jawaher², Sedaghat, Alireza^2,4, Shariati, Gholamreza^2,5, shariatig@yahoo.com, Galehdari, Hamid¹, galehdari187@yahoo.com

Source: Molecular Genetics & Genomics; Sep2022, Vol. 297 Issue 5, p1289-1300, 12p

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Association of HLA-DR2-Related Haplotype (HLA-DRB5*01-DRB1*1501-DQB1*0602) in Patients with Multiple Sclerosis in Khuzestan Province.

Authors: DELFAN, Nooshin, GALEHDARI, Hamid, GHANBARI MARDASI, Farideh, ZABIHI, Rezvan, LATIFI PAKDEHI, Tahereh, SEIFI, Tahereh, MAJDINASAB, Nastaran

Source: Iranian Journal of Child Neurology; Summer2021, Vol. 15 Issue 3, p35-46, 12p

Subject Terms: GENETICS of multiple sclerosis, CASE-control method, HAPLOTYPES

Geographic Terms: IRAN

Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing.

Authors: Negahdari, Samira, Zamani, Mina, Seifi, Tahereh, Sedighzadeh, Sahar, Mazaheri, Neda, Zeighami, Jawaher, Sedaghat, Alireza, Saberi, Alihossein, Hamid, Mohammad, keikhaei, Bijan, Radpour, Ramin, Shariati, Gholamreza, Galehdari, Hamid

Source: International Journal of Preventive Medicine; 2020, Vol. 11 Issue 1, p1-7, 7p

Subject Terms: BLOOD platelets, BLOOD diseases, GENES, FAMILY history (Medicine), GENETIC mutation

News and Reports: Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome.

Authors: Zamani, Mina^1,2, Seifi, Tahereh^1,2, Zeighami, Jawaher¹, Mazaheri, Neda^1,2, Jahangirnezhad, Emad¹, Gholamzadeh, Minoo¹, Sedaghat, Alireza^1,3, Shariati, Gholamreza^1,4 gshariati@yahoo.com, Galehdari, Hamid^1,2 galehdari187@yahoo.com

Source: Basic & Clinical Neuroscience. Jul/Aug2020, Vol. 11 Issue 4, p549-555. 8p.

Subject Terms: *GENETIC disorders, *GENETIC testing, *SYNDROMES, *GENES, *GENOTYPES

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Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran.

Authors: Delfan, Nooshin, Galehdari, Hamid, Shafiei, Mohammad, Ghanbari-Mardasi, Farideh, Latifi, Tahereh, Majdinasab, Nastaran, Seifi, Tahereh

Source: Iranian Journal of Neurology; 2018, Vol. 17 Issue 4, p154-60, 1p

Subject Terms: HLA histocompatibility antigens, GENETICS of multiple sclerosis, HAPLOTYPES