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Research Paper: Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis.
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- Basic & Clinical Neuroscience, 2017, v. 8, n. 4, p. 279, doi. 10.18869/nirp.bcn.8.4.279
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- Publication type:
- Article
Analysis and Identification of Rare and Prevalent Breakpoints in Chromosomal rearrangements in Adult and Pediatric with B-Acute Lymphoblastic Leukemia (B-ALL): A Systematic Review.
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- Iranian Journal of Pediatric Hematology & Oncology, 2024, v. 14, n. 3, p. 227, doi. 10.18502/ijpho.v14i3.15992
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- Publication type:
- Article
In-silico study to identify the pathogenic single nucleotide polymorphisms in the coding region of CDKN2A gene.
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- Iranian Journal of Pediatric Hematology & Oncology, 2021, v. 11, n. 2, p. 114, doi. 10.18502/ijpho.v11i2.5844
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- Publication type:
- Article
MicroRNAs as a New Molecular Biomarker for Diagnosis and Prognosis of T-cell Acute Lymphoblastic Leukemia (T-ALL): A Systematic Review.
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- Iranian Journal of Pediatric Hematology & Oncology, 2020, v. 10, n. 3, p. 183
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- Publication type:
- Article
Induced pluripotent stem cells (iPSCs) based approaches for hematopoietic cancer therapy.
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- Iranian Journal of Pediatric Hematology & Oncology, 2019, v. 9, n. 2, p. 117
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- Publication type:
- Article
A novel heteroplasmic mutation in mitochondrial tRNAArg gene associated with non-dystrophic myotonias.
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- Acta Neurologica Belgica, 2020, v. 120, n. 3, p. 573, doi. 10.1007/s13760-018-1042-5
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- Publication type:
- Article
Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome.
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- Cardiology Journal, 2018, v. 25, n. 1, p. 113, doi. 10.5603/CJ.a2017.0104
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- Publication type:
- Article
The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study.
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- International Journal of Reproductive Biomedicine, 2019, v. 17, n. 8, p. 557, doi. 10.18502/ijrm.v17i8.4821
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- Publication type:
- Article
Protective effect of Berberis vulgaris on Fenton reaction-induced DNA cleavage.
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- Avicenna Journal of Phytomedicine, 2019, v. 9, n. 3, p. 213
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- Publication type:
- Article
Evaluation of the antioxidant activity of berberis vulgaris juice on the production of free radicals and inhibition of DNA fragmentation.
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- Avicenna Journal of Phytomedicine, 2015, v. 5, p. 14
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- Publication type:
- Article
Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism.
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- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 8, p. 857, doi. 10.1515/jpem-2017-0084
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- Publication type:
- Article
A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia.
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- Cellular & Molecular Neurobiology, 2009, v. 29, n. 2, p. 225, doi. 10.1007/s10571-008-9315-9
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- Publication type:
- Article
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.
- Published in:
- 2008
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- Publication type:
- journal article
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients.
- Published in:
- Neurological Sciences, 2008, v. 29, n. 6, p. 489, doi. 10.1007/s10072-008-1026-y
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- Publication type:
- Article
Apolipoprotein E Gene Polymorphism in Iranian Coronary Atherosclerosis Patients Candidate for Coronary Artery Bypass Graft.
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- Iranian Journal of Basic Medical Sciences, 2013, v. 16, n. 7, p. 841
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- Publication type:
- Article
The POLG Gene Polymorphism in Iranian Varicocele-Associated Infertility Patients.
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- Iranian Journal of Basic Medical Sciences, 2012, v. 15, n. 2, p. 739
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- Publication type:
- Article
Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia.
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- Iranian Journal of Basic Medical Sciences, 2011, v. 14, n. 3, p. 219
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- Publication type:
- Article
A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome.
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- Archives of Iranian Medicine (AIM), 2016, v. 19, n. 6, p. 403
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- Publication type:
- Article
Heterobimetallic Pt<sup>II</sup>‐Au<sup>I</sup> Complexes Comprising Unsymmetrical 1,1‐Bis(diphenylphosphanyl)methane Bridges: Synthesis, Photophysical, and Cytotoxic Studies.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 10, p. 1360, doi. 10.1002/ejic.201801297
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- Publication type:
- Article
Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis.
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- Journal of Cardiovascular & Thoracic Research, 2020, v. 12, n. 3, p. 221, doi. 10.34172/jcvtr.2020.37
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- Publication type:
- Article
Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects.
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- Journal of Cardiovascular & Thoracic Research, 2018, v. 10, n. 1, p. 41, doi. 10.15171/jcvtr.2018.07
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- Publication type:
- Article
Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP).
- Published in:
- 2021
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- Publication type:
- journal article
Mitochondrial Genetic Variation in Iranian Infertile Men with Varicocele.
- Published in:
- International Journal of Fertility & Sterility, 2016, v. 10, n. 3, p. 303
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- Publication type:
- Article
Mutation analysis of TNP1 gene in infertile men with varicocele.
- Published in:
- Iranian Journal of Reproductive Medicine, 2014, v. 12, n. 4, p. 257
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- Publication type:
- Article
Molecular Analysis of tRNAGlu, Trp, Ala, Asp Genes of mtDNA in Patients with Long QT Syndrome.
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- Journal of Mazandaran University of Medical Sciences (JMUMS), 2014, v. 24, n. 116, p. 141
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- Publication type:
- Article
Upregulation of miR-222 in both Helicobacter pylori-infected and noninfected gastric cancer patients.
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- Journal of Genetics, 2016, v. 95, n. 4, p. 991, doi. 10.1007/s12041-016-0728-9
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- Publication type:
- Article
Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease.
- Published in:
- Applied Biochemistry & Biotechnology, 2020, v. 191, n. 3, p. 1326, doi. 10.1007/s12010-020-03275-0
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- Publication type:
- Article
Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients.
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- Applied Biochemistry & Biotechnology, 2020, v. 190, n. 3, p. 896, doi. 10.1007/s12010-019-03125-8
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- Publication type:
- Article
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09410-y
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- Publication type:
- Article
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09410-y
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- Publication type:
- Article
بررسی ژنومیک و بیوانفورماتیکی تغییرات نوکلئوتیدی نواحی کدینگ ژن CCDC103 در بیماران مبتلا به تترالوژی فالوت (TOF): یک نوع نقص قلبی مادرزادی
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- Journal of Birjand University of Medical Sciences, 2024, v. 31, n. 1, p. 48
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- Publication type:
- Article
Mitochondrial Mutations in tRNA<sup>Glu</sup> and Cytochrome h Genes Associated with Iranian Congenial Heart Disease.
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- International Cardiovascular Research Journal, 2016, v. 10, n. 4, p. 193
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- Publication type:
- Article
میتوکندري در بیماران ایرانی مبتلا به پولیپوز DNA توالی D-loop تجزیه و تحلیل ژنتیکی ناحیه آدنوماتوز خانوادگی: یک مطالعه مورد-شاهدي
- Published in:
- Journal of Rafsanjan University of Medical Sciences, 2023, v. 21, n. 12, p. 1307
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- Publication type:
- Article
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).
- Published in:
- Physiology International, 2022, v. 109, n. 2, p. 261, doi. 10.1556/2060.2022.00224
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- Publication type:
- Article
The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis.
- Published in:
- Iranian Journal of Child Neurology, 2015, v. 9, n. 1, p. 37
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- Publication type:
- Article
Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich's Ataxia.
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- Iranian Journal of Child Neurology, 2014, v. 8, n. 1, p. 32
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- Publication type:
- Article
Increased Prevalence 12308 A > G mutation in Mitochondrial tRNA<sup>Leu (CUN)</sup> Gene Associated with earlier Age of Onset in Friedreich Ataxia.
- Published in:
- 2011
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- Publication type:
- Journal Article
Increased Prevalence 12308 A > G mutation in Mitochondrial tRNA<sup>Leu (CUN)</sup> Gene Associated with earlier Age of Onset in Friedreich Ataxia.
- Published in:
- Iranian Journal of Child Neurology, 2011, v. 5, n. 4, p. 25
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- Publication type:
- Article