240 results on '"Khorram Khorshid, Hamid Reza"'
Search Results
2. Artificial intelligence breakthroughs in pioneering early diagnosis and precision treatment of breast cancer: A multimethod study
3. Uptake and outcomes of implementing non-invasive prenatal testing (Prenatal Reflex DNA testing) into first-trimester contingent screening protocols for trisomy 21, 18, 13: A study protocol
4. Discriminative features in White-Sutton syndrome: literature review and first report in Iran
5. Identification of causative gene mutation in an Iranian family with coloboma and nephropathy using whole exome sequencing
6. Protective effects of Herbal Compound (IM253) on the inflammatory responses and oxidative stress in a mouse model of multiple sclerosis
7. Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.
8. RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in two distinct Iranian families: Case report and literature review
9. Discriminative features in White-Sutton syndrome: literature review and first report in Iran
10. Association of MMP2 and MMP9 gene polymorphisms with nonsyndromic cleft lip/palate in an Iranian population
11. A simple, rapid and economic manual method for human sperm DNA extraction in genetic and epigenetic studies
12. Reactive oxygen species-induced alterations in H19-Igf2 methylation patterns, seminal plasma metabolites, and semen quality
13. Analysis of the genes encoding the spp24 protein in human and mouse and identification of interacting proteins
14. BMP2 and BMP4 variations and risk of non-syndromic cleft lip and palate
15. Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations
16. Whole Exome Sequencing Identified the Causative Mutation in a 4-Year-Old Female with Mulibrey Nanism: A Case Report
17. Combination of IMOD™ and Arbidol to increase their immunomodulatory effects as a novel medicine to prevent and cure influenza and some other infectious diseases
18. A Panel of Circulating microRNAs as a Potential Biomarker for the Early Detection of Gastric Cancer
19. Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends
20. ELISPOT analysis of a new CTL based DNA vaccine for HIV-1 using GM-CSF in DNA prime/peptide boost strategy: GM-CSF induced long-lived memory responses
21. RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations
22. Association of rs2013162 and rs2235375 Polymorphisms in IRF6 Gene with Susceptibility to Non-Syndromic Cleft Lip and Palate
23. Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion)
24. Downregulation of E-cadherin expression in breast cancer by promoter hypermethylation and its relation with progression and prognosis of tumor
25. Safety and Effectiveness of SeptimebTM in Patients with COVID-19 Referred to a Teaching and Referral Hospital: An Uncontrolled Clinical Trial Study (Phase II).
26. Electrophysiology of Human Gametes: A Systematic Review
27. Analysis of the CTAGE5 P521A Variation with the Risk of Familial Idiopathic Basal Ganglia Calcification in an Iranian Population
28. Disease waves of SARS-CoV-2 in Iran closely mirror global pandemic trends
29. Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome
30. Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa
31. Plasminogen Activator Inhibitor 1 and Methylenetetrahydrofolate Reductase Gene mutations in Iranian Women with Polycystic Ovary Syndrome
32. Shikonin ameliorates experimental autoimmune encephalomyelitis (EAE) via immunomodulatory, anti-apoptotic and antioxidative activity
33. MiR‐4485‐3p expression reduced in spermatozoa of men with idiopathic asthenozoospermia
34. 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
35. RPE65 and retinal dystrophy: Report of new and recurrent mutations
36. Iranome: A catalog of genomic variations in the Iranian population
37. Interleukin 1 alpha (IL1A) polymorphisms and risk of endometriosis in Iranian population: a case-control study
38. MicroRNA profiling in spermatozoa of men with unexplained asthenozoospermia
39. MFSD8 gene mutations; evidence for phenotypic heterogeneity
40. Why have microRNA biomarkers not been translated from bench to clinic?
41. Comparison of three methods for mitochondria isolation from the human liver cell line (HepG2)
42. Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease
43. Comments on the AZFc markers used for screening of Yq microdeletions
44. Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia.
45. Genetic aspects of idiopathic asthenozoospermia as a cause of male infertility.
46. Interleukin 1 alpha (IL1A) polymorphisms and risk of endometriosis in Iranian population: a case-control study.
47. An overview of microRNAs: Biology, functions, therapeutics, and analysis methods
48. Reactive oxygen species-induced alterations in H19-Igf2 methylation patterns, seminal plasma metabolites, and semen quality
49. Correlation between important genes of mTOR pathway (PI3K and KIT) in Iranian women with sporadic breast cancer
50. Genetic aspects of idiopathic asthenozoospermia as a cause of male infertility
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