Works by Talebi, Saeed
Results: 49
A BIM-Based Solution for the Optimisation of Fire Safety Measures in the Building Design.
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- Sustainability (2071-1050), 2022, v. 14, n. 3, p. 1626, doi. 10.3390/su14031626
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- Article
Tolerance Management in Construction: A Conceptual Framework.
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- Sustainability (2071-1050), 2020, v. 12, n. 3, p. 1039, doi. 10.3390/su12031039
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- Article
The importance of CDC27 in cancer: molecular pathology and clinical aspects.
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- Cancer Cell International, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12935-021-01860-9
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- Article
Comparable vitamin D3 metabolism in the endometrium of patients with recurrent spontaneous abortion and fertile controls.
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- Molecular Reproduction & Development, 2015, v. 82, n. 5, p. 356, doi. 10.1002/mrd.22486
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- Article
Quantification of sperm specific mRNA transcripts ( PRM1, PRM2, and TNP2) in teratozoospermia and normozoospermia: New correlations between mRNA content and morphology of sperm.
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- Molecular Reproduction & Development, 2015, v. 82, n. 1, p. 26, doi. 10.1002/mrd.22440
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- Article
Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population.
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- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 4, p. 1, doi. 10.1002/mgg3.2421
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- Article
Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees.
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- Cell Journal (Yakhteh), 2016, v. 18, n. 3, p. 397
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- Article
An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.
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- Cell Journal (Yakhteh), 2016, v. 18, n. 2, p. 229
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- Article
Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 10, p. 1215, doi. 10.1515/jpem-2016-0096
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- Article
First Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants.
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- Archives of Iranian Medicine (AIM), 2024, v. 27, n. 12, p. 700, doi. 10.34172/aim.31593
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- Article
Engineering and Kinetic Stabilization of the Therapeutic Enzyme Anabeana variabilis Phenylalanine Ammonia Lyase.
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- Applied Biochemistry & Biotechnology, 2013, v. 171, n. 7, p. 1805, doi. 10.1007/s12010-013-0450-5
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- Article
A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian Pedigree.
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- Avicenna Journal of Medical Biotechnology, 2017, v. 9, n. 3, p. 146
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- Article
The Effect of Sortilin Silencing on Ovarian Carcinoma Cells.
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- Avicenna Journal of Medical Biotechnology, 2014, v. 6, n. 3, p. 169
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- Article
RNA Sequencing of CD4<sup>+</sup> T Cells in Relapsing–Remitting Multiple Sclerosis Patients at Relapse: Deciphering the Involvement of Novel genes and Pathways.
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- Journal of Molecular Neuroscience, 2021, v. 71, n. 12, p. 2628, doi. 10.1007/s12031-021-01878-8
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- Article
Wiskott--Aldrich syndrome with possible congenital Cytomegalovirus infection: A diagnostic dilemma.
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- National Medical Journal of India, 2021, v. 34, n. 1, p. 24
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- Article
Identification and characterization of the largest deletion in the PCCA gene causing severe acute early-onset form of propionic acidemia.
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- Molecular Genetics & Genomics, 2023, v. 298, n. 4, p. 905, doi. 10.1007/s00438-023-02023-3
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- Article
Methylmalonic Acidemia Diagnosis by Laboratory Methods.
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- Reports of Biochemistry & Molecular Biology, 2016, v. 5, n. 1, p. 1
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- Article
Optimized Condition for Enhanced Soluble-Expression of Recombinant Mutant Anabaena Variabilis Phenylalanine Ammonia Lyase.
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- Advanced Pharmaceutical Bulletin, 2014, v. 4, n. 3, p. 261, doi. 10.5681/apb.2014.038
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- Article
An Iranian Congenital Adrenal Hypoplasia Patient with Elevated Testosterone in Infancy due to a Novel Pathogenic Frameshift Variant in NR0B1.
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- International Journal of Endocrinology, 2021, p. 1, doi. 10.1155/2021/4367028
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- Article
Comparative Molecular and Microbiologic Diagnosis of Vaginal Colonization by Group B Streptococcus in Pregnant Women during Labor.
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- Iranian Journal of Basic Medical Sciences, 2010, v. 13, n. 4, p. 183
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- Article
Efficient generation of functional hepatocyte-like cells from menstrual blood-derived stem cells.
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- Journal of Tissue Engineering & Regenerative Medicine, 2015, v. 9, n. 11, p. E124, doi. 10.1002/term.1715
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- Article
Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b).
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- 2020
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- journal article
Comparison of the effects of nobiletin and letrozole on the activity and expression of aromatase in the MCF-7 breast cancer cell line.
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- Biochemistry & Cell Biology, 2017, v. 95, n. 4, p. 468, doi. 10.1139/bcb-2016-0206
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- Article
Impact of Vitamin A Supplementation on RAR Gene Expression in Multiple Sclerosis Patients.
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- Journal of Molecular Neuroscience, 2013, v. 51, n. 2, p. 478, doi. 10.1007/s12031-013-0090-9
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- Publication type:
- Article
Sodium Butyrate as a Histone Deacetylase Inhibitor Affects Toll-Like Receptor 4 Expression in Colorectal Cancer Cell Lines.
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- Immunological Investigations, 2019, v. 48, n. 7, p. 759, doi. 10.1080/08820139.2019.1595643
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- Article
Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach.
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- Hereditas, 2023, v. 160, n. 1, p. 1, doi. 10.1186/s41065-023-00281-0
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- Article
An Integrated Model for Multi-Mode Resource-Constrained Multi-Project Scheduling Problems Considering Supply Management with Sustainable Approach in the Construction Industry under Uncertainty Using Evidence Theory and Optimization Algorithms.
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- Buildings (2075-5309), 2023, v. 13, n. 8, p. 2023, doi. 10.3390/buildings13082023
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- Article
Unintended Consequences of Productivity Improvement Strategies on Safety Behaviour of Construction Labourers; A Step toward the Integration of Safety and Productivity.
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- Buildings (2075-5309), 2022, v. 12, n. 3, p. 317, doi. 10.3390/buildings12030317
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- Article
Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi−Bickel Syndrome.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.601566
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- Article
Producing Recombinant mTEX101; a Murine Testis Specific Protein.
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- Journal of Reproduction & Infertility, 2009, v. 10, n. 3, p. 193
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- Article
Investigating the Relationship between Faculty Members` Demographic Features and Learning and Education Quality in Fars Payame Noor University and Shiraz University of Medical Sciences.
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- Iranian Journal of Medical Education, 2015, v. 14, n. 10, p. 834
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- Article
Integration of resource supply management and scheduling of construction projects using multi-objective whale optimization algorithm and NSGA-II.
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- Soft Computing - A Fusion of Foundations, Methodologies & Applications, 2024, v. 28, n. 11/12, p. 6983, doi. 10.1007/s00500-023-09467-0
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- Article
Deploying Geometric Dimensioning and Tolerancing in Construction.
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- Buildings (2075-5309), 2020, v. 10, n. 4, p. 62, doi. 10.3390/buildings10040062
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- Article
Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells.
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- Iranian Journal of Allergy, Asthma & Immunology, 2015, v. 14, n. 2, p. 179
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- Article
Griscelli Syndrome Type 2: A Rare Case With Apparently Normal Skin and Hair Pigmentation.
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- Acta Medica Iranica, 2020, v. 58, n. 1, p. 38
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- Article
Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01097-9
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- Publication type:
- Article
The effect of Setarud (IMOD™) on angiogenesis in transplanted human ovarian tissue to nude mice.
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- Iranian Journal of Reproductive Medicine, 2015, v. 13, n. 10, p. 591
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- Article
Investigation on estrogen receptor alpha gene polymorphisms in Iranian women with recurrent pregnancy loss.
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- Iranian Journal of Reproductive Medicine, 2014, v. 12, n. 6, p. 395
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- Publication type:
- Article
In silico Analysis of Two Novel Variants in the Pyruvate Carboxylase (PC) Gene Associated with the Severe Form of PC Deficiency.
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- Iranian Biomedical Journal, 2023, v. 27, n. 5, p. 307, doi. 10.61186/ibj.27.5.307
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- Article
Whole Exome Sequencing Reveals a XPNPEP3 Novel Mutation Causing Nephronophthisis in a Pediatric Patient.
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- 2020
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- Publication type:
- journal article
Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient.
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- 2020
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- Publication type:
- journal article
Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
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- 2016
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- Publication type:
- journal article
Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
- Published in:
- Iranian Biomedical Journal, 2016, v. 20, n. 5, p. 1
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- Publication type:
- Article
High resolution melting technique for molecular epidemiological studies of cystic echinococcosis: differentiating G1, G3, and G6 genotypes of Echinococcus granulosus sensu lato.
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- Parasitology Research, 2013, v. 112, n. 10, p. 3441, doi. 10.1007/s00436-013-3523-z
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- Article
Author Correction: Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model.
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- 2023
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- Correction Notice
Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17232-w
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- Article
New Report of a Different Clinical Presentation of CD151 Splicing Mutation (c.351+2T>C): Could TSPAN11 be Considered as a Potential Modifier Gene for CD151?
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- Molecular Syndromology, 2022, v. 13, n. 3, p. 212, doi. 10.1159/000519633
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- Article
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.
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- Metabolic Brain Disease, 2017, v. 32, n. 5, p. 1685, doi. 10.1007/s11011-017-0048-7
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- Article
The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile.
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- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-75
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- Article