Found: 31
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The Role of Non-Coding RNAs in Mitochondrial Dysfunction of Alzheimer’s Disease.
- Published in:
- Journal of Molecular Neuroscience, 2024, v. 74, n. 4, p. 1, doi. 10.1007/s12031-024-02262-y
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- Publication type:
- Article
A Novel Pathogenic Mutation in WNK1 Gene Causing HSAN Type II in Three Siblings.
- Published in:
- Journal of Molecular Neuroscience, 2024, v. 74, n. 4, p. 1, doi. 10.1007/s12031-024-02282-8
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- Publication type:
- Article
Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.
- Published in:
- 2016
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- Publication type:
- journal article
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
- Published in:
- 2016
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- Publication type:
- journal article
Restoration of correct splicing in IVSI-110 mutation of β-globin gene with antisense oligonucleotides: implications and applications in functional assay development.
- Published in:
- Iranian Journal of Basic Medical Sciences, 2017, v. 20, n. 6, p. 700, doi. 10.22038/IJBMS.2017.8840
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- Publication type:
- Article
Genetic variations of complement factor H and C3 in patients with thrombotic thrombocytopenic purpura (TTP) in North-West of Iran.
- Published in:
- Journal of Nephropathology, 2018, v. 7, n. 2, p. 74, doi. 10.15171/jnp.2018.18
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- Publication type:
- Article
A new insight on serum microRNA expression as novel biomarkers in breast cancer patients.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 11, p. 19199, doi. 10.1002/jcp.28656
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- Publication type:
- Article
Molecular Study of STin2 (Intron 2) Variant of the SLC6A4 Gene in Children and Adolescents with Attention-deficit Hyperactivity Disorder.
- Published in:
- Iranian Journal of Psychiatry & Behavioral Sciences / Progress in Psychiatry & Behavioral Sciences, 2022, v. 16, n. 4, p. 1, doi. 10.5812/ijpbs-122884
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- Publication type:
- Article
Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases.
- Published in:
- Journal of Prenatal Medicine, 2013, v. 7, n. 3, p. 32
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- Publication type:
- Article
A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01165-4
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- Publication type:
- Article
miR‐449a: A Promising Biomarker and Therapeutic Target in Cancer and Other Diseases.
- Published in:
- Cell Biochemistry & Biophysics, 2024, v. 82, n. 3, p. 1629, doi. 10.1007/s12013-024-01322-9
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- Publication type:
- Article
One Novel Frameshift Mutation on Exon 64 of COL7A1 Gene in an Iranian Individual Suffering Recessive Dystrophic Epidermolysis Bullosa.
- Published in:
- Annals of Clinical & Laboratory Science, 2015, v. 45, n. 5, p. 582
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- Publication type:
- Article
Molecular analysis and prevalence of Huntington disease in northwestern Iran.
- Published in:
- Turkish Journal of Medical Sciences, 2017, v. 47, n. 6, p. 1880, doi. 10.3906/sag-1510-25
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- Publication type:
- Article
The hopeful anticancer role of oleuropein in breast cancer through histone deacetylase modulation.
- Published in:
- Journal of Cellular Biochemistry, 2019, v. 120, n. 10, p. 17042, doi. 10.1002/jcb.28965
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- Publication type:
- Article
Downregulation of HDAC2 and HDAC3 via oleuropein as a potent prevention and therapeutic agent in MCF‐7 breast cancer cells.
- Published in:
- Journal of Cellular Biochemistry, 2019, v. 120, n. 6, p. 9172, doi. 10.1002/jcb.28193
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- Publication type:
- Article
Inhibition of MEK/ERK1/2 Signaling Affects the Fatty Acid Composition of HepG2 Human Hepatic Cell Line.
- Published in:
- BioImpacts, 2012, v. 2, n. 3, p. 145, doi. 10.5681/bi.2012.019
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- Publication type:
- Article
Molecular Evaluation of Ex3 VNTR Polymorphism of the DRD4 Gene in Patients With Autism Spectrum Disorder.
- Published in:
- Iranian Journal of Child Neurology, 2022, v. 16, n. 4, p. 23, doi. 10.22037/ijcn.v16i4.34289
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- Publication type:
- Article
Evaluation of Association Between HLA Class II DR4-DQ8 Haplotype and Type I Diabetes Mellitus in Children of East Azerbaijan State of Iran.
- Published in:
- Advanced Pharmaceutical Bulletin, 2015, v. 5, n. 1, p. 137, doi. 10.5681/apb.2015.020
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- Publication type:
- Article
Cloning of Soluble Human Stem Cell Factor in pET-26b(+) Vector.
- Published in:
- Advanced Pharmaceutical Bulletin, 2014, v. 4, n. 1, p. 91, doi. 10.5681/apb.2014.014
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- Publication type:
- Article
Construction of Yeast Recombinant Expression Vector Containing Human Epidermal Growth Factor (hEGF).
- Published in:
- Advanced Pharmaceutical Bulletin, 2013, v. 3, n. 2, p. 473, doi. 10.5681/apb.2013.079
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- Publication type:
- Article
Construction of pPIC9 Recombinant Vector Containing Human Stem Cell Factor.
- Published in:
- Advanced Pharmaceutical Bulletin, 2013, v. 3, n. 2, p. 303, doi. 10.5681/apb.2013.049
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- Publication type:
- Article
Narrower insight to SIRT1 role in cancer: A potential therapeutic target to control epithelial–mesenchymal transition in cancer cells.
- Published in:
- Journal of Cellular Physiology, 2018, v. 233, n. 6, p. 4443, doi. 10.1002/jcp.26302
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- Publication type:
- Article
Mutual interaction of lncRNAs and epigenetics: focusing on cancer.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s43042-023-00404-2
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- Publication type:
- Article
Over-expression of mir-181a-3p in serum of breast cancer patients as diagnostic biomarker.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09272-4
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- Publication type:
- Article
Over-expression of mir-181a-3p in serum of breast cancer patients as diagnostic biomarker.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09272-4
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- Publication type:
- Article
Identifi cation of multi-exon deletion in the COL7A1 gene underlying dystrophic epidermolysis bullosa by whole-exome sequencing.
- Published in:
- Our Dermatology Online / Nasza Dermatologia Online, 2021, v. 12, n. 4, p. 412, doi. 10.7241/ourd.20214.13
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- Publication type:
- Article
The HLA-G 14bp insertion/deletion polymorphism in Women with Recurrent Spontaneous Abortion.
- Published in:
- 2014
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- Publication type:
- Journal Article
The HLA-G 14-bp Insertion/ Deletion Polymorphism in Recurrent Spontaneous Abortion among Iranian Women.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2014, v. 13, n. 5, p. 364
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- Publication type:
- Article
Evaluation of a newly discovered breast cancer susceptibility locus at 6q25.1 in Iranian Azari-Turkish women.
- Published in:
- Contemporary Oncology / Współczesna Onkologia, 2016, v. 20, n. 4, p. 308, doi. 10.5114/wo.2016.61851
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- Publication type:
- Article
Detection of Hemophilia A Carriers in Azeri Turkish Population of Iran.
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- Clinical & Applied Thrombosis/Hemostasis, 2015, v. 21, n. 8, p. 755, doi. 10.1177/1076029614526638
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- Publication type:
- Article
NUCB2/Nesfatin-1: A Potent Meal Regulatory Hormone and its Role in Diabetes.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 2, p. 105, doi. 10.1016/j.ejmhg.2016.10.003
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- Publication type:
- Article