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Your search keyword '"Omrani M"' showing total 219 results

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219 results on '"Omrani M"'

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1. Spontaneous Intra-cerebral Hemorrhage; Initial Clinical And CT Findings Tabriz - Emam and Razi Hospitals (1996 - 99)

7. Hematopoietic reconstitution dynamics of mobilized- and bone marrow-derived human hematopoietic stem cells after gene therapy

11. Association between miRNAs expression and multiple sclerosis pathogenesis: A novel therapeutic approach

12. Application of machine learning to remove false positive genomic position in vector insertion site data

14. The quasi-universality of nestedness in the structure of quantitative plant-parasite interactions

20. Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184

21. Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316)

22. Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia

23. Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies

24. 3D protein-based bilayer artificial skin for guided scarless healing of full-thickness burn wounds in vivo

28. FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men

30. Study on Macrobenthic communities in the range of fish cage-culture area (before breeding) in the southern Caspian Sea (Mazandaran coast-Kelarabad)

37. Theoretical and Experimental Investigation of Optical Properties of ZnS Zig-Zag Thin Films.

38. A Comparison between External versus Internal Lateral Osteotomy in Rhinoplasty

41. Autologous Hematopoietic Stem Cell Transplantation (AHSCT): An Evolving Treatment Avenue in Multiple Sclerosis

42. Mutational screening of theNR5A1in azoospermia

45. Association of SRD5A2gene mutations with risk of hypospadias in the Iranian population

47. A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family

49. Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients

50. Association of HLA alleles with autism

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