Search Results - "Mozafari, N."

Photo-catalytic dye degradation of methyl orange using zirconia–zeolite nanoparticles by Mansouri, M, Mozafari, N, Bayati, B, Setareshenas, N

“…In this research, the dye photo-catalytic removal was investigated using zirconia ( ZrO 2 ) nanocatalysts, zeolite (Ze), ZrO 2 –Ze with different percentages…”
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Acute localized exanthematous pustulosis caused by enoxaparin by Mozafari, N., Farjami, M., Jamali, E., Rostami, H., Ketabi, Y.

“…Notably, enoxaparin has not been described to cause acute localized exanthematous pustulosis (ALEP). Herein, we present a case of a woman with a cutaneous drug…”
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Cultured allogeneic fibroblast injection vs. fibroblasts cultured on amniotic membrane scaffold for dystrophic epidermolysis bullosa treatment by Moravvej, H., Abdollahimajd, F., Naseh, M.H., Piravar, Z., Abolhasani, E., Mozafari, N., Niknejad, H.

“…Summary Background Different methods of fibroblast application have been examined to treat recessive dystrophic epidermolysis bullosa (RDEB). Objectives To…”
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Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects by Timmer, C., Davids, M., Nieuwdorp, M., Levels, J.H.M., Langendonk, J.G., Breederveld, M., Ahmadi Mozafari, N., Langeveld, M.

“…Urea cycle disorders (UCDs) are a group of rare inherited metabolic diseases causing hyperammonemic encephalopathy. Despite intensive dietary and…”
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Serum 25-hydroxy vitamin D level in patients with pemphigus and its association with disease severity by Moravvej, H., Mozafari, N., Younespour, S.

“…Summary Background There is a growing number of studies suggesting a key role for vitamin D in the pathogenesis and progression of autoimmune disorders. Aim To…”
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A new homozygous nonsense mutation in LAMA3A underlying laryngo‐onycho‐cutaneous syndrome by Barzegar, M., Mozafari, N., Kariminejad, A., Asadikani, Z., Ozoemena, L., McGrath, J.A.

“…Summary Laryngo‐onycho‐cutaneous (LOC) syndrome is a subtype of autosomal recessive junctional epidermolysis bullosa in which there is prominent skin and…”
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Hearing status in patients with vitiligo by Rahimi, Hoda, Mozafari, Nikoo, Bastaninejad, Shahin, Tehranchinia, Zohreh, Samani, Nourullah Aghaebrahimi

“…Vitiligo is an acquired disorder characterized by depigmented macules and patches that result from a progressive loss of functional melanocytes. During…”
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Immunization with HIV-1 envelope T20-encoding DNA vaccines elicits cross-clade neutralizing antibody responses by Stenler, S., Lundin, K. E., Hansen, L., Petkov, S., Mozafari, N., Isaguliants, M., Blomberg, P., Smith, C. I. E., Goldenberg, D. M., Chang, C.-H., Ljungberg, K., Hinkula, J., Wahren, B.

“…Background: Genetic immunization is expected to induce the expression of antigens in a native form. The encoded peptide epitopes are presented on endogenous…”
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Terbinafine susceptibility and genotypic heterogeneity in clinical isolates of Trichophyton mentagrophytes by random amplified polymorphic DNA (RAPD) by Alipour, M., Mozafari, N.A.

“…The four RAPD systems tested in the present study have aimed at investigating DNA fingerprinting of Trichophyton mentagrophytes strains and the correlation…”
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Assessing Oligonucleotide Binding to Double-Stranded DNA by Mozafari, Negin, Umek, Tea

“…Sequence-specific targeting of double-stranded DNA (dsDNA) using synthetic oligonucleotides (ONs) has been under investigation in different therapeutic…”
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Large-scale expansions of Friedreich's ataxia GAA•TTC repeats in an experimental human system: role of DNA replication and prevention by LNA-DNA oligonucleotides and PNA oligomers by Rastokina, Anastasia, Cebrián, Jorge, Mozafari, Negin, Mandel, Nicholas H, Smith, C I Edvard, Lopes, Massimo, Zain, Rula, Mirkin, Sergei M

“…Abstract Friedreich's ataxia (FRDA) is caused by expansions of GAA•TTC repeats in the first intron of the human FXN gene that occur during both…”
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纤维母细胞注射与羊膜纤维母细胞治疗RDEB的对比 by Moravvej, H., Abdollahimajd, F., Naseh, M.-H., Piravar, Z., Abolhasani, E., Mozafari, N., Niknejad, H.

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An enriched social behavioural information diffusion model in social networks by Mozafari, Niloofar, Hamzeh, Ali

“…Online social networks have recently become an innovative and effective method for spreading information among people around the world. Information diffusion,…”
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Fibroblast injection vs. fibroblasts on amniotic membrane in RDEB by Moravvej, H., Abdollahimajd, F., Naseh, M.‐H., Piravar, Z., Abolhasani, E., Mozafari, N., Niknejad, H.

“…Summary Epidermolysis bullosa (EB) is a blistering disorder caused by at least 18 variable gene mutations (meaning ‘mistakes’ in certain genes). Recessive…”
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816 Iranian genetic skin and connective tissue disorders project: Epidermolysis bullosa by Vahidnezhad, H., Youssefian, L., Zeinali, S., Saeidian, A., Touati, A., Sotoudeh, S., Daneshpazhooh, M., Hamid, M., Mozafari, N., Mahmoudi, H., Uitto, J.

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Intralesional botulinum toxin-A injection for the treatment of multiple eccrine hidrocystomas by Gheisari, Mehdi, Hamedani, Behnaz, Robati, RezaM, Mozafari, Nikoo

“…Multiple eccrine hidrocystomas (MEH) are benign cystic lesions of the sweat gland ducts. They are characterized by translucent, skin-colored or bluish…”
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385 Whole genome homozygosity mapping to identify candidate genes in epidermolysis bullosa in consanguineous families by Vahidnezhad, H., Youssefian, L., Zeinali, S., Sotoude, S., Barzegar, M.R., Mozafari, N., Saeidian, A.H., Hakonarson, H., Uitto, J.

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382 COL7A1 mutation detection in a cohort of 133 consanguineous families with recessive dystrophic epidermolysis bullosa: Comparison of disease-targeted next generation sequencing panel vs. traditional Sanger sequencing by Youssefian, L., Vahidnezhad, H., Zeinali, S., Barzegar, M.R., Sotoudeh, S., Mozafari, N., Ertel, A., Fortina, P., Saeidian, A.H., Uitto, J.

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521 Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa by Zahabiyon, M., Vahidnezhad, H., Youssefian, L., Saeidian, A., Zeinali, S., Sotoudeh, S., Mozafari, N., Bradfield, J., Kim, C., Hakonarson, H., Uitto, J.

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Chemical Modifications and Design Influence the Potency of Huntingtin Anti-Gene Oligonucleotides by Saher, Osama, Zaghloul, Eman M, Umek, Tea, Hagey, Daniel W, Mozafari, Negin, Danielsen, Mathias B, Gouda, Alaa S, Lundin, Karin E, Jørgensen, Per T, Wengel, Jesper, Smith, C I Edvard, Zain, Rula

“…Huntington's disease is a neurodegenerative, trinucleotide repeat (TNR) disorder affecting both males and females. It is caused by an abnormal increase in the…”
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