Search Results - "Darvish, H."

Evolutionary trend of exceptionally long human core promoter short tandem repeats by Ohadi, M., Mohammadparast, S., Darvish, H.

“…Short tandem repeats (STRs) are variable elements that play a significant role in genome evolution by creating and maintaining quantitative genetic variation…”
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First principles computational investigation on the possibility of Pt-decorated SiC hexagonal sheet as a suitable material for oxygen reduction reaction by Darvish Ganji, M., Agheb, R., Darvish Ganji, H., Ashrafian, S.

“…First principles calculations play a significant role in developing and optimizing new energy storage and conversion materials especially at the nanoscale. In…”
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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly by Darvish, H, Esmaeeli-Nieh, S, Monajemi, G B, Mohseni, M, Ghasemi-Firouzabadi, S, Abedini, S S, Bahman, I, Jamali, P, Azimi, S, Mojahedi, F, Dehghan, A, Shafeghati, Y, Jankhah, A, Falah, M, Soltani Banavandi, M J, Ghani, M, Ghani-Kakhi, M, Garshasbi, M, Rakhshani, F, Naghavi, A, Tzschach, A, Neitzel, H, Ropers, H H, Kuss, A W, Behjati, F, Kahrizi, K, Najmabadi, H

“…Primary microcephaly (MCPH) is a genetically heterogeneous disorder showing an autosomal recessive mode of inheritance. Affected individuals present with head…”
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A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome by Rahimi-Aliabadi, S, Daftarian, N, Ahmadieh, H, Emamalizadeh, B, Jamshidi, J, Tafakhori, A, Ghaedi, H, Noroozi, R, Taghavi, S, Ahmadifard, A, Alehabib, E, Andarva, M, Shokraeian, P, Atakhorrami, M, Darvish, H

“…Purpose Jalili syndrome is an autosomal recessive disorder characterized by simultaneous appearance of cone-rod dystrophy (CRD) and amelogenesis imperfecta…”
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Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder by Farashi, S., Ohadi, M., Hosseinkhani, S., Darvish, H., Mirabzadeh, A.

“…Accumulating evidence of population association studies support the hypothesis that the high heritability of major psychiatric disorders is a combination of…”
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Novel evidence of the involvement of calreticulin in major psychiatric disorders by Ohadi, M., Mirabzadeh, A., Esmaeilzadeh-Gharehdaghi, E., Rezazadeh, M., Hosseinkhanni, S., Oladnabi, M., Firouzabadi, S. Ghasemi, Darvish, H.

“…Calreticulin (CALR) is a multi-functional protein that is strictly conserved across species. Two mRNA transcripts have been recognized for the CALR gene in…”
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Dominant and Protective Role of the CYTH4 Primate-Specific GTTT-Repeat Longer Alleles Against Neurodegeneration by Rezazadeh, M., Gharesouran, J., Movafagh, A., Taheri, M., Darvish, H., Emamalizadeh, B., Shahmohammadibeni, N., Khorram Khorshid, H. R., Behmanesh, M., Sahraian, M. A., Ohadi, M.

“…Primate-specific genes and regulatory mechanisms could provide insight into human brain functioning and disease. In a genome-scale analysis of the entire…”
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Single-operator Ultrasound-guided Intravenous Line Placement by Emergency Nurses Reduces the Need for Physician Intervention in Patients with Difficult-to-establish Intravenous Access by Weiner, Scott G., MD, MPH, Sarff, Allison R., MS, Esener, Dasia E., MD, Shroff, Sunil D., MD, Budhram, Gavin R., MD, RDMS, Switkowski, Karen M., MS, MPH, Mostofi, Matthew B., DO, Barus, Richard W., BS, Coute, Ryan A., BS, Darvish, Amir H., MD, RDMS

“…Abstract Background Emergency physicians (EPs) have become facile with ultrasound-guided intravenous line (USIV) placement in patients for whom access is…”
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Exceptional human core promoter nucleotide compositions by Darvish, H., Nabi, M. Olad, Firouzabadi, S. Ghasemi, Karimlou, M., Heidari, A., Najmabadi, H., Ohadi, M.

“…The proximal promoter sequences contain basic motifs for the expression of the downstream genes. We present genome-scale computational analyses of the 120-bp…”
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Core promoter STRs: Novel mechanism for inter-individual variation in gene expression in humans by Heidari, A., Nariman Saleh Fam, Z., Esmaeilzadeh-Gharehdaghi, E., Banan, M., Hosseinkhani, S., Mohammadparast, S., Oladnabi, M., Ebrahimpour, M.R., Soosanabadi, M., Farokhashtiani, T., Darvish, H., Firouzabadi, S. Ghasemi, Farashi, S., Najmabadi, H., Ohadi, M.

“…In a genome-scale analysis of the composition of core promoter sequences, we have recently shown that approximately 25% of the human protein-coding genes have…”
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Optimization of 241Am-Be emission direction in neutron porosity tools for improving the precision in determining the porosity in calcite formation by F Rahmani, H Darvish Motevalli

“…Investigation of Hydrocarbon reservoir is important, so it is essential to predict and explore them precisely. One of the methods is well logging, which can…”
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Haplotypes across the human caveolin 1 gene upstream purine complex significantly alter gene expression: Implication in neurodegenerative disorders by Heidari, A., Hosseinkhani, S., Talebi, S., Meshkani, R., Esmaeilzadeh-Gharedaghi, E., Banan, M., Darvish, H., Ohadi, M.

“…We have previously reported a polymorphic purine complex at the 1.5kb upstream region of the human caveolin 1 (CAV1) gene that is conserved across several…”
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HLA-DRA is associated with Parkinson's disease in Iranian population by Jamshidi, J., Movafagh, A., Emamalizadeh, B., Zare Bidoki, A., Manafi, A., Ghasemi Firouzabadi, S., Shahidi, G.-A., Kazeminasab, S., Petramfar, P., Fazeli, A., Motallebi, M., Mortazavi-Tabatabaei, S. A., Kowsari, A., Jafarian, Z., Darvish, H.

“…Summary The rs3129882, a noncoding variant in HLA‐DR, was found to be associated with Parkinson's disease (PD) using several genome‐wide association studies…”
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The human caveolin 1 gene upstream purine complex and neurodegeneration—A common signature by Heidari, A, Behmanesh, M, Sahraian, M.A, Meshkani, R, Darvish, H, Najmabadi, H, Ohadi, M

“…Abstract The caveolin 1 gene ( CAV1 ) is over-expressed in experimental animal models of multiple sclerosis (MS). Increased expression of this gene has also…”
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Phenotypic heterogeneity and full penetrance in a family with dopa-responsive dystonia by Karkheiran, S, Hubert, B, Moghaddam, HN, Darvish, H, Paisán-Ruiz, C

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Superior Labial Artery Aneurysm after Mouth Laceration by Mostofi, Matthew B., Darvish, Amir H., Weiner, Scott G.

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Hepatitis B virus infection in patients with blood disorders: a concise review in pediatric study by Mansouri, N, Movafagh, A, Sayad, A, Ghafouri-Fard, S, Darvish, H, Zare-Abdollahi, D, Emamalizadeh, B, Shahvaisizadeh, F, Ghaedi, H, Bastami, M, Kayyal, M, Hashemi, M, Heidari, Mh, Nejatizadeh, A, Zamani, M

“…Childhood Hepatitis B virus (HBV) infection causes both medical and public health challenges. Infants who acquire HBV parentally have up to 90% risk of…”
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The Efficacy of Prophylactic Ondansetron, Droperidol, Perphenazine, and Metoclopramide in the Prevention of Nausea and Vomiting After Major Gynecologic Surgery by Desilva, P. H. D. P., Darvish, Amir H., McDonald, Steven M., Cronin, Mary K., Clark, Kathy

“…The prophylactic antiemetic efficacy of intravenous (IV) ondansetron, droperidol, perphenazine, and metoclopramide was evaluated in a prospective, doubleblind…”
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Clinical and molecular aspects of sjogren-larsson syndrome reported in an Iranian consanguineous family with triplet affected individuals by Tzschach, A., Najmabadi, H., Kahrizi, K., Ropers, H., Kuss, A., Behjati, F., Darvish, H., Hemmati, S., Husayni, M., Garshasbi, M.

“…Background: Sjogren Larsson Syndrome (SLS; OMIM: 270200) is an autosomal recessive neurocutaneous disorder characterized by mental retardation, congenital…”
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Investigation of genetic causes of intellectual disability in kerman province, South East of Iran by Fayruzabadi, S. Ghasemi, Jafari, E., Ghadami, Sh, Sabbagh, F., Kavoosi, Gh. R., Najmabadi, H., Abedinni, S. Sedigheh, Bahman, I., Darvish, H., Muhseni, M., Behjati, F., Banavandi, M. J. Sultani, Kahrizi, K.

“…Background: Intellectual disability (ID) has a worldwide prevalence of 1-3% and results from extraordinary heterogeneous. To shed more light on the causes of…”
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