Works matching AU Khorram Khorshid, Hamid Reza
Results: 82
Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia.
- Published in:
- 2020
- By:
- Publication type:
- journal article
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
- Published in:
- 2019
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- Publication type:
- Report
Healing Influence of Melilotus Officinalis Herbal Extract on Experimental Autoimmune Encephalomyelitis in C57BL/6 Mice.
- Published in:
- Iranian Journal of Pharmaceutical Research, 2020, v. 19, n. 4, p. 321, doi. 10.22037/ijpr.2020.113808.14505
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- Publication type:
- Article
Do we need a replacement medication for influenza with good efficacy?
- Published in:
- DARU: Journal of Pharmaceutical Sciences, 2014, v. 22, p. 1, doi. 10.1186/s40199-014-0084-3
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- Publication type:
- Article
Do we need a replacement medication for influenza with good efficacy?
- Published in:
- 2014
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- Publication type:
- journal article
Effects of IMOD™ and Angipars™ on mouse D-galactose-induced model of aging.
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- DARU: Journal of Pharmaceutical Sciences, 2012, v. 20, p. 1, doi. 10.1186/2008-2231-20-68
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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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- Publication type:
- Article
Prevalence of intratubular germ cell neoplasia in cryptorchid testes of infertile men.
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- Iranian Journal of Reproductive Medicine, 2013, v. 11, n. 4, p. 339
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- Publication type:
- Article
Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 635, doi. 10.3390/ijms18030635
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- 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
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- Publication type:
- Article
Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics.
- Published in:
- 2013
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- Publication type:
- journal 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
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- Publication type:
- Article
Association Study of Transforming Growth Factor Alpha TaqI Polymorphism and the Risk of Cleft Lip and/or Palate in an Iranian Population.
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- Birth Defects Research, 2017, v. 109, n. 17, p. 1386, doi. 10.1002/bdr2.1125
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- Publication type:
- Article
Plasminogen Activator Inhibitor 1 and Methylenetetrahydrofolate Reductase Gene mutations in Iranian Women with Polycystic Ovary Syndrome.
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- American Journal of Reproductive Immunology, 2012, v. 68, n. 5, p. 400, doi. 10.1111/aji.12002
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- 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.
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- Acta Medica Iranica, 2013, v. 51, n. 4, p. 209
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- Publication type:
- Article
Discrepancy in the results of Y chromosome microdeletions in an Iranian population.
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- Journal of Human Reproductive Sciences, 2011, v. 4, n. 3, p. 157, doi. 10.4103/0974-1208.92295
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- Publication type:
- Article
Association of glutathione S-transferases M1, P1 and T1 variations and risk of late-onset Alzheimer’s disease.
- Published in:
- Neurological Research, 2018, v. 40, n. 1, p. 41, doi. 10.1080/01616412.2017.1390902
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- Publication type:
- Article
A panel of noncoding RNAs in non–small‐cell lung cancer.
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- Journal of Cellular Biochemistry, 2019, v. 120, n. 5, p. 8280, doi. 10.1002/jcb.28111
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- Publication type:
- Article
Curcumin ameliorates experimental autoimmune encephalomyelitis in a C57BL/6 mouse model.
- Published in:
- Drug Development Research, 2019, v. 80, n. 5, p. 629, doi. 10.1002/ddr.21540
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- Publication type:
- Article
The effect of paternal age on semen quality and fertilization outcome in men with normal sperm DNA compaction, reactive oxygen species, and total antioxidant capacity levels.
- Published in:
- Turkish Journal of Urology, 2019, v. 45, n. 3, p. 164, doi. 10.5152/tud.2019.74944
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- 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
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- Publication type:
- Article
Beginning at the ends: telomere and telomere-based cancer therapeutics.
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- Molecular Genetics & Genomics, 2024, v. 300, n. 1, p. 1, doi. 10.1007/s00438-024-02206-6
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- 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.
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- Medical Principles & Practice, 2015, v. 24, n. 4, p. 351, doi. 10.1159/000430842
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- Publication type:
- Article
Reconstruction of mammalian oocytes by germinal vesicle transfer: A systematic review.
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- International Journal of Reproductive Biomedicine, 2017, v. 15, n. 10, p. 601
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- Publication type:
- Article
Association study of Glutathione S-Transferase polymorphisms and risk of endometriosis in an Iranian population.
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- International Journal of Reproductive Biomedicine, 2016, v. 14, n. 4, p. 241
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- 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
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- Publication type:
- Article
Association study of the TNF-α −1031T/C and VEGF + 450G/C polymorphisms with susceptibility to endometriosis.
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- Gynecological Endocrinology, 2013, v. 29, n. 11, p. 974, doi. 10.3109/09513590.2013.824956
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- Publication type:
- Article
Effects of Ectoine on Behavior and Candidate Genes Expression in ICV-STZ Rat Model of Sporadic Alzheimer's Disease.
- Published in:
- Advanced Pharmaceutical Bulletin, 2017, v. 7, n. 4, p. 629, doi. 10.15171/apb.2017.075
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- Publication type:
- Article
Effects of Herbal Compound (IMOD) on Behavior and Expression of Alzheimer's Disease Related Genes in Streptozotocin-Rat Model of Sporadic Alzheimer's Disease.
- Published in:
- Advanced Pharmaceutical Bulletin, 2017, v. 7, n. 3, p. 491, doi. 10.15171/apb.2017.060
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- Publication type:
- Article
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.
- Published in:
- Neurogenetics, 2025, v. 26, n. 1, p. 1, doi. 10.1007/s10048-024-00789-1
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- 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
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- 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
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- Publication type:
- Article
Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico Analysis.
- Published in:
- Clinical Genetics, 2025, v. 107, n. 3, p. 366, doi. 10.1111/cge.14658
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- Publication type:
- Article
Ccr2-64i and Ccr5 Δ32 Polymorphisms in Patients with Late-Onset Alzheimer's disease; A Study from Iran (Ccr2-64i And Ccr5 Δ32 Polymorphisms in Alzheimer's disease).
- Published in:
- Iranian Journal of Basic Medical Sciences, 2012, v. 15, n. 4, p. 937
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- Publication type:
- Article
The Association between TNF-alpha Gene Polymorphisms and Endometriosis in An Iranian Population.
- Published in:
- International Journal of Fertility & Sterility, 2019, v. 13, n. 1, p. 6, doi. 10.22074/ijfs.2019.5542
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- Publication type:
- Article
Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A.
- Published in:
- 2025
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- Publication type:
- Case Study
Detection of CRISPR/Cas9-Mediated Fetal Hemoglobin Reactivation in Erythroblasts Derived from Cord Blood-Hematopoietic Stem Cells.
- Published in:
- Molecular Biotechnology, 2025, v. 67, n. 4, p. 1695, doi. 10.1007/s12033-024-01155-0
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- 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
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- 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
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- Publication type:
- Article
Electrophysiology of Human Gametes: A Systematic Review.
- Published in:
- World Journal of Men's Health, 2022, v. 40, n. 3, p. 442, doi. 10.5534/wjmh.210107
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- Publication type:
- Article
MiR‐4485‐3p expression reduced in spermatozoa of men with idiopathic asthenozoospermia.
- Published in:
- Andrologia, 2020, v. 52, n. 3, p. 1, doi. 10.1111/and.13539
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- Publication type:
- Article
MicroRNA profiling in spermatozoa of men with unexplained asthenozoospermia.
- Published in:
- Andrologia, 2019, v. 51, n. 6, p. 1, doi. 10.1111/and.13284
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- Publication type:
- Article
Association of MMP2 and MMP9 gene polymorphisms with nonsyndromic cleft lip/palate in an Iranian population.
- Published in:
- Journal of Dental Research, Dental Clinics, Dental Prospects, 2023, v. 17, n. 3, p. 149, doi. 10.34172/joddd.2023.40640
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- Publication type:
- Article
Comparison of three methods for mitochondria isolation from the human liver cell line (HepG2).
- Published in:
- Gastroenterology & Hepatology from Bed to Bench, 2016, v. 9, n. 2, p. 105
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- 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
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- Publication type:
- Article
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
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- Publication type:
- Article
The study of association between reduced folate carrier 1 (RFC1) polymorphism and non-syndromic cleft lip/palate in Iranian population.
- Published in:
- BioImpacts, 2017, v. 7, n. 4, p. 263, doi. 10.15171/bi.2017.31
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- Publication type:
- Article
Association of Vascular Endothelial Growth Factor (VEGF) +405 G<C Polymorphism with Endometriosis in an Iranian Population.
- Published in:
- Journal of Reproduction & Infertility, 2010, v. 11, n. 1, p. 33
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- 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
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- 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
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- Publication type:
- Article