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المؤلفون: Samaneh Maleknia, Mohammad Ali Sahraian, Kaveh Kavousi, Saeed Talebi, Zahra Salehi, Abdorreza Naser Moghadasi, Maryam Izad, Fahimeh Palizban
المصدر: Journal of Molecular Neuroscience. 71:2628-2645
مصطلحات موضوعية: Multiple sclerosis, RNA, General Medicine, Biology, medicine.disease, Transcriptome, Cellular and Molecular Neuroscience, Immune system, Transcription (biology), Cancer research, medicine, KEGG, Gene, B cell receptor signaling pathway
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::bdcfc6fc59577ac5f9a5dc077b920660Test
https://doi.org/10.1007/s12031-021-01878-8Test -
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المؤلفون: Mohammad Ali Sahraian, Saeed Talebi, Zahra Salehi, Mohammad Keramatipour, Maryam Izad, Seyed Shahriar Arab, Abdorreza Naser Moghadasi
المصدر: Genomics. 113:2645-2655
مصطلحات موضوعية: 0106 biological sciences, Multiple Sclerosis, Disease, Iran, Biology, 01 natural sciences, Genome, Pathogenesis, 03 medical and health sciences, Exome Sequencing, Genetics, medicine, Humans, Missense mutation, Exome, Exome sequencing, DNA Polymerase III, 030304 developmental biology, 0303 health sciences, Multiple sclerosis, Heterozygote advantage, medicine.disease, Pedigree, Consanguineous Marriage, 010606 plant biology & botany
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3c1d10e7f0c6bda5b70de8d88ee8e7Test
https://doi.org/10.1016/j.ygeno.2021.06.008Test -
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المؤلفون: Nazanin Atieh Kazemi-Sefat, Kazem Mousavizadeh, Roya Sajed, Kaveh Kavousi, Golnaz Ensieh Kazemi-Sefat, Mohammad Keramatipour, Saeed Talebi
المصدر: Cancer Cell International
Cancer Cell International, Vol 21, Iss 1, Pp 1-11 (2021)مصطلحات موضوعية: Cancer Research, Tumor suppressor gene, Review, Cell cycle, Biology, medicine.disease_cause, lcsh:RC254-282, Metastasis, 03 medical and health sciences, 0302 clinical medicine, Downregulation and upregulation, Cancer stem cell, Neoplasms, Upregulation, Genetics, medicine, lcsh:QH573-671, CDC27 protein, 030304 developmental biology, Anaphase-Promoting complex–cyclosome, 0303 health sciences, lcsh:Cytology, Cancer, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, medicine.disease, Oncology, 030220 oncology & carcinogenesis, Downregulation, Tumorigenesis, Cancer cell, Cancer research, Carcinogenesis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc00b730c8bef44f017d5ee3cac8343Test
https://pubmed.ncbi.nlm.nih.gov/33750395Test -
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المؤلفون: Maryam Eghbali, Kiyana Sadat Fatemi, Shadab Salehpour, Maryam Abiri, Hassan Saei, Saeed Talebi, Nasrin Alipour Olyaei, Vahid Reza Yassaee, Mohammad Hossein Modarressi
المصدر: Frontiers in Genetics, Vol 11 (2021)
Frontiers in Geneticsمصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Glycogen storage disease type VI, Genetic counseling, glycogen storage diseases, Biology, Genetic analysis, novel causative variants, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Genetics, medicine, pharmacogenetic variants, whole-exome sequencing, Gene, Exome, Genetics (clinical), Exome sequencing, Original Research, Sanger sequencing, secondary/incidental findings, medicine.disease, lcsh:Genetics, 030104 developmental biology, Mendelian inheritance, symbols, Molecular Medicine, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b59c9dac9a3963ede3cc62f589338040Test
https://www.frontiersin.org/articles/10.3389/fgene.2020.601566/fullTest -
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المؤلفون: Rozita Hoseini, Saeed Talebi, Soraya Gholizad-kolveiri, Rasoul Alizadeh, Nakysa Hooman, Hasan Otukesh, Mansoureh Akouchekian
المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)مصطلحات موضوعية: Male, 0301 basic medicine, Proband, lcsh:Internal medicine, Diacylglycerol Kinase, lcsh:QH426-470, Mutation, Missense, Case Report, 030105 genetics & heredity, Biology, Consanguinity, Young Adult, 03 medical and health sciences, symbols.namesake, Exon, Catalytic Domain, Exome Sequencing, Atypical hemolytic uremic syndrome, DGKE, Genetics, medicine, Humans, Missense mutation, lcsh:RC31-1245, Genetics (clinical), Exome sequencing, Atypical Hemolytic Uremic Syndrome, Sanger sequencing, Hemolytic-uremic syndrome, Homozygote, Whole exome sequencing, Familial hemolytic uremic syndrome, Microangiopathic hemolytic anemia, medicine.disease, Pedigree, lcsh:Genetics, 030104 developmental biology, Protein computational analysis, symbols, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd87bae826eecb61223374a989cdac14Test
https://doi.org/10.1186/s12881-020-01097-9Test -
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المؤلفون: Elham Salehi Siavashani, Saeed Talebi, Mitra Nourbakhsh, Mehdi Vafadar, Ali Sharifi-Zarchi, Masoud Garshasbi, Mona Nourbakhsh, Maryam Razzaghy-Azar
المصدر: Clinical biochemistry. 90
مصطلحات موضوعية: Male, 030213 general clinical medicine, medicine.medical_specialty, Heterozygote, Ataxia, Clinical Biochemistry, 030204 cardiovascular system & hematology, medicine.disease_cause, 03 medical and health sciences, Exon, 0302 clinical medicine, Metabolic Diseases, Renal Dialysis, Internal medicine, Medicine, Humans, Ethanol metabolism, Coma, Child, Alcohol dehydrogenase, Mutation, biology, medicine.diagnostic_test, business.industry, Methanol, Metabolic disorder, Alcohol Dehydrogenase, General Medicine, Exons, medicine.disease, Zinc, Endocrinology, Treatment Outcome, Liver, biology.protein, medicine.symptom, business, Liver function tests, Alcoholic Intoxication, Metabolism, Inborn Errors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a72f7f33607f52c22fc748137427f807Test
https://pubmed.ncbi.nlm.nih.gov/33539811Test -
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المؤلفون: Saeed Talebi, Zahra Noroozi, Maryam Eghbali, Ali Rabbani, Mehri Najafi, Fatemeh Yazarlou, Mohammad Hossein Modarressi, Marjan Shakiba, Maryam Abiri, Hosein Alimadadi, Parastoo Rostami
المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)مصطلحات موضوعية: G6PC, Genotype-phenotype correlation, Monosaccharide Transport Proteins, lcsh:Medicine, Context (language use), Biology, Glycogen Storage Disease Type I, Iran, Antiporters, Frameshift mutation, Genotype, medicine, Missense mutation, Glycogen storage disease, Humans, Pharmacology (medical), Gene, Genetics (clinical), Genetic Association Studies, Genetics, Research, lcsh:R, General Medicine, medicine.disease, Autozygosity mapping, Phenotype, Mutation, Microsatellite, Novel variants, GSD1b
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21f7e4bddde56a9a84dffe43945d8f3cTest
http://europepmc.org/articles/PMC6995048Test -
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المؤلفون: Rezvan Bagheri, Saeed Talebi, Leila Eini, Mojgan Alaeddini, Shahroo Etemad-Moghadam, Razieh Bitazar
المصدر: Gene. 782:145542
مصطلحات موضوعية: 0301 basic medicine, Apoptosis, Bone Marrow Cells, Flow cytometry, 03 medical and health sciences, 0302 clinical medicine, Cell Line, Tumor, Genetics, medicine, Humans, MTT assay, Amnion, Viability assay, Cell Proliferation, medicine.diagnostic_test, biology, Liver Neoplasms, Mesenchymal stem cell, Mesenchymal Stem Cells, General Medicine, Flow Cytometry, Proliferating cell nuclear antigen, Squamous carcinoma, 030104 developmental biology, Cell culture, Culture Media, Conditioned, 030220 oncology & carcinogenesis, Carcinoma, Squamous Cell, Cancer research, biology.protein, Drug Screening Assays, Antitumor
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::051b1af555732cb363e2df1f682a01ebTest
https://doi.org/10.1016/j.gene.2021.145542Test -
9Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes
المؤلفون: Mohammad Keramatipour, Saeed Talebi, Seyede Zahra Sajedi, Golnaz-Ensieh Kazemi-sefat, Seyyed Mojtaba Mohaddes Ardebili, Masoumeh Razipour, Aria Setoodeh, Neda Mohajer, Jalal Gharesouran, Mona Entezam, Elaheh Alavinejad
المصدر: Metabolic Brain Disease. 32:1685-1691
مصطلحات موضوعية: 0301 basic medicine, Genotype, Phenylalanine hydroxylase, Mutant, Locus (genetics), Minisatellite Repeats, Iran, Gene mutation, Polymerase Chain Reaction, Biochemistry, 03 medical and health sciences, Cellular and Molecular Neuroscience, Exon, Gene Frequency, Phenylketonurias, Prevalence, Humans, Allele, Gene, Genetics, biology, Phenylalanine Hydroxylase, Molecular biology, Introns, 030104 developmental biology, Haplotypes, Mutation, biology.protein, Female, Allelic heterogeneity, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b402763adaaca7fb7a2b6220a12bb1bTest
https://doi.org/10.1007/s11011-017-0048-7Test -
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المؤلفون: Cordian Beyer, Somaieh Kazemnejad, Amir-Hassan Zarnani, Saeed Talebi, Adib Zendedel, Mohammad Taghi Joghataei, Fereshteh Azedi, Kazem Mousavizadeh, Masoud Mehrpour
المصدر: Brain Research. 1723:146401
مصطلحات موضوعية: Male, 0301 basic medicine, Neuroimmunomodulation, Ischemia, Pharmacology, Brain Ischemia, Melatonin, 03 medical and health sciences, 0302 clinical medicine, Animals, Medicine, Rats, Wistar, Molecular Biology, Neuroinflammation, Inflammation, biology, Microglia, TREM2, business.industry, General Neuroscience, Hypoxia (medical), medicine.disease, Rats, Stroke, 030104 developmental biology, medicine.anatomical_structure, Melatonin receptor 1B, Reperfusion Injury, Reperfusion, biology.protein, Neurology (clinical), NeuN, medicine.symptom, business, hormones, hormone substitutes, and hormone antagonists, 030217 neurology & neurosurgery, Signal Transduction, Developmental Biology, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5edd36cfab79e86af433a016dcb8160Test
https://doi.org/10.1016/j.brainres.2019.146401Test