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Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Shikonin ameliorates experimental autoimmune encephalomyelitis (EAE) via immunomodulatory, anti‐apoptotic and antioxidative activity.
- Published in:
- Journal of Pharmacy & Pharmacology, 2020, v. 72, n. 12, p. 1970, doi. 10.1111/jphp.13364
- By:
- Publication type:
- Article
The Relationship between KIT Copy Number Variation, Protein Expression, and Angiogenesis in Sporadic Breast Cancer.
- Published in:
- Reports of Biochemistry & Molecular Biology, 2020, v. 9, n. 1, p. 40, doi. 10.29252/rbmb.9.1.40
- By:
- Publication type:
- Article
The Relationship between KIT Copy Number Variation, Protein Expression, and Angiogenesis in Sporadic Breast Cancer.
- Published in:
- Reports of Biochemistry & Molecular Biology, 2020, v. 8, n. 4, p. 40, doi. 10.29252/rbmb.9.1.40
- By:
- Publication type:
- Article
A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 11, p. 1, doi. 10.1002/mgg3.70031
- By:
- Publication type:
- Article
RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in two distinct Iranian families: Case report and literature review.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 4, p. 1, doi. 10.1002/mgg3.2435
- By:
- Publication type:
- Article
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
- Published in:
- 2019
- By:
- Publication type:
- Report
Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
- Published in:
- International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 635, doi. 10.3390/ijms18030635
- By:
- Publication type:
- Article
Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics.
- Published in:
- BMC Nephrology, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2369-14-190
- By:
- Publication type:
- Article
Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Methodological errors in screening of Yq microdeletion in Iranian azoospermic men.
- Published in:
- 2012
- By:
- Publication type:
- Letter
RPE65 and retinal dystrophy: Report of new and recurrent mutations.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 3, p. 1, doi. 10.1002/jgm.3154
- By:
- Publication type:
- Article
Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease.
- Published in:
- Medical Principles & Practice, 2015, v. 24, n. 4, p. 351, doi. 10.1159/000430842
- By:
- Publication type:
- Article
The effect of Setarud (IMOD™) on angiogenesis in transplanted human ovarian tissue to nude mice.
- Published in:
- Iranian Journal of Reproductive Medicine, 2015, v. 13, n. 10, p. 591
- By:
- Publication type:
- Article
Prevalence of intratubular germ cell neoplasia in cryptorchid testes of infertile men.
- Published in:
- Iranian Journal of Reproductive Medicine, 2013, v. 11, n. 4, p. 339
- By:
- Publication type:
- Article
Vitamin D Receptor (VDR) Polymorphisms and Late-Onset Alz-heimer's Disease: An Association Study.
- Published in:
- Iranian Journal of Public Health, 2013, v. 42, n. 11, p. 1253
- By:
- Publication type:
- Article
Reactive oxygen species-induced alterations in H19-Igf2 methylation patterns, seminal plasma metabolites, and semen quality.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 2, p. 241, doi. 10.1007/s10815-018-1350-y
- By:
- Publication type:
- Article
A simple, rapid and economic manual method for human sperm DNA extraction in genetic and epigenetic studies.
- Published in:
- Middle East Fertility Society Journal, 2018, v. 23, n. 3, p. 216, doi. 10.1016/j.mefs.2017.12.005
- By:
- Publication type:
- Article
Genetic aspects of idiopathic asthenozoospermia as a cause of male infertility.
- Published in:
- Human Fertility, 2020, v. 23, n. 2, p. 83, doi. 10.1080/14647273.2018.1504325
- By:
- Publication type:
- Article
Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families.
- Published in:
- Familial Cancer, 2018, v. 17, n. 2, p. 213, doi. 10.1007/s10689-017-0023-9
- By:
- Publication type:
- Article
A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families.
- Published in:
- Familial Cancer, 2018, v. 17, n. 2, p. 209, doi. 10.1007/s10689-017-0018-6
- By:
- Publication type:
- Article
DNA Repair Gene XRCC1 and XRCC4 Variations and Risk of Endometriosis: An Association Study.
- Published in:
- Gynecologic & Obstetric Investigation, 2015, v. 80, n. 2, p. 85, doi. 10.1159/000366444
- By:
- Publication type:
- Article
Safety and Effectiveness of SeptimebTM in Patients with COVID-19 Referred to a Teaching and Referral Hospital: An Uncontrolled Clinical Trial Study (Phase II).
- Published in:
- Journal of Iranian Medical Council (JIMC), 2023, v. 6, n. 2, p. 328, doi. 10.18502/jimc.v6i2.12243
- By:
- Publication type:
- Article
Interleukin 1 alpha (IL1A) polymorphisms and risk of endometriosis in Iranian population: a case-control study.
- Published in:
- Gynecological Endocrinology, 2020, v. 36, n. 2, p. 135, doi. 10.1080/09513590.2019.1631790
- By:
- Publication type:
- Article
Association of common variations of the E-cadherin with endometriosis.
- Published in:
- Gynecological Endocrinology, 2015, v. 31, n. 11, p. 899, doi. 10.3109/09513590.2015.1101436
- By:
- Publication type:
- Article
Association study of the TNF-α −1031T/C and VEGF + 450G/C polymorphisms with susceptibility to endometriosis.
- Published in:
- Gynecological Endocrinology, 2013, v. 29, n. 11, p. 974, doi. 10.3109/09513590.2013.824956
- By:
- Publication type:
- Article
A Panel of Circulating microRNAs as a Potential Biomarker for the Early Detection of Gastric Cancer.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2022, v. 14, n. 4, p. 278, doi. 10.18502/ajmb.v14i4.10482
- By:
- Publication type:
- Article
Association of rs2013162 and rs2235375 Polymorphisms in IRF6 Gene with Susceptibility to Non-Syndromic Cleft Lip and Palate.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2022, v. 14, n. 2, p. 181, doi. 10.18502/ajmb.v14i2.8885
- By:
- Publication type:
- Article
Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2021, v. 13, n. 4, p. 230, doi. 10.18502/ajmb.v13i4.7214
- By:
- Publication type:
- Article
Methylation Analysis of P16, RASSF1A, RPRM, and RUNX3 in Circulating Cell-Free DNA for Detection of Gastric Cancer: A Validation Study.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2020, v. 12, n. 2, p. 99
- By:
- Publication type:
- Article
Interaction Effect of RsaI and BamHI Polymorphisms of TGFα, BMP2 and BMP4 on the Occurrence of Non-Syndromic Cleft Lip and Palate in Iranian Patients.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2018, v. 10, n. 4, p. 248
- By:
- Publication type:
- Article
Association between rs6759298 and Ankylosing Spondylitis in Iranian Population.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2018, v. 10, n. 3, p. 163
- By:
- Publication type:
- Article
Association of the WNT3 Variations and the Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2018, v. 10, n. 3, p. 168
- By:
- Publication type:
- Article
Clinically Significant Dysregulation of hsa-miR-30d-5p and hsa-let-7b Expression in Patients with Surgically Resected Non-Small Cell Lung Cancer.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2018, v. 10, n. 2, p. 98
- By:
- Publication type:
- Article
Altered miR-223 Expression in Sputum for Diagnosis of Non-Small Cell Lung Cancer.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2017, v. 9, n. 4, p. 189
- By:
- Publication type:
- Article
The Effects of Melilotus officinalis Extract on Expression of Daxx, Nfkb and Vegf Genes in the Streptozotocin-Induced Rat Model of Sporadic Alzheimer's Disease.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2017, v. 9, n. 3, p. 133
- By:
- Publication type:
- Article
Neuroprotective Effects of Herbal Extract (Rosa canina, Tanacetum vulgare and Urtica dioica) on Rat Model of Sporadic Alzheimer's Disease.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2016, v. 8, n. 3, p. 120
- By:
- Publication type:
- Article
Association of Transforming Growth Factor Alpha Polymorphisms with Nonsyndromic Cleft Lip and Palate in Iranian Population.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2015, v. 7, n. 4, p. 168
- By:
- Publication type:
- Article
An Association Study on IL16 Gene Polymorphisms with the Risk of Sporadic Alzheimer's Disease.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2015, v. 7, n. 3, p. 128
- By:
- Publication type:
- Article
Original Article. Maternal Supplementary Folate Intake, Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C Polymorphisms and the Risk of Orofacial Cleft in Iranian Children.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2015, v. 7, n. 2, p. 80
- By:
- Publication type:
- Article
Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2013, v. 5, n. 4, p. 251
- By:
- Publication type:
- Article
Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2012, v. 4, n. 4, p. 193
- By:
- Publication type:
- Article
Fetal Sex Determination using Non-Invasive Method of Cell-free Fetal DNA in Maternal Plasma of Pregnant Women During 6<sup>th</sup>-10<sup>th</sup> Weeks of Gestation.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2011, v. 3, n. 4, p. 201
- By:
- Publication type:
- Article
Association of CALHM1 gene polymorphism with late onset Alzheimer's disease in Iranian population.
- Published in:
- 2010
- By:
- Publication type:
- Journal Article
Association of CALHM1 Gene Polymorphism with Late Onset Alzheimer's Disease in Iranian Population.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2010, v. 2, n. 3, p. 153
- By:
- Publication type:
- Article
Lack of Association between Tumor Necrosis Factor-alpha -308 G/A Polymorphism and Risk of Developing Late-Onset Alzheimer's Disease in an Iranian Population.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2009, v. 1, n. 3, p. 193
- By:
- Publication type:
- Article
New Variations in the Promoter Regions of Human DOCK4 and RAP1A Genes, and Coding Regions of RAP1A in Sporadic Breast Tumors.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2009, v. 1, n. 2, p. 117
- By:
- Publication type:
- Article
Plasminogen Activator Inhibitor 1 and Methylenetetrahydrofolate Reductase Gene mutations in Iranian Women with Polycystic Ovary Syndrome.
- Published in:
- American Journal of Reproductive Immunology, 2012, v. 68, n. 5, p. 400, doi. 10.1111/aji.12002
- By:
- Publication type:
- Article
Early Fetal Gender Determination Using Real-Time PCR Analysis of Cell-free Fetal DNA During 6<sup>th</sup>-10<sup>th</sup> Weeks of Gestation.
- Published in:
- Acta Medica Iranica, 2013, v. 51, n. 4, p. 209
- By:
- Publication type:
- Article
Discrepancy in the results of Y chromosome microdeletions in an Iranian population.
- Published in:
- Journal of Human Reproductive Sciences, 2011, v. 4, n. 3, p. 157, doi. 10.4103/0974-1208.92295
- By:
- Publication type:
- Article