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Sepideh Shahkarami

Showing results (11-20 of 35) with videos related to

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Digestive Diseases and Sciences|December 4, 2014
Significance of IL-1RA Polymorphism in Iranian Patients with Inflammatory Bowel DiseaseNasser Ebrahimi Daryani, Maryam Sadr, Shirin Moossavi, et al.
Cell Journal|February 25, 2023
Minimal Residual Disease Detection Using Gene Scanning Analysis, Fluorescent Fragment Analysis, and Capillary Electrophoresis for IgH Rearrangement in Adult B-Lineage Acute Lymphoblastic Leukemia: A Cross-Sectional StudySepideh Shahkarami, Samareh Younesian, Shahrbano Rostami, et al.
Digestive Diseases (Basel, Switzerland)|August 23, 2018
Association of T Helper 1 Cytokine Gene Single Nucleotide Polymorphisms with Ulcerative Colitis and Crohn's DiseaseNasser Ebrahimi Daryani, Maryam Sadr, Samaneh Soltani, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 2, 2022
A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case ReportShaghayegh Sadeghmousavi, Sepideh Shahkarami, Elham Rayzan, et al.
Journal of Medical Case Reports|July 17, 2023
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothersElham Rayzan, Mona Sadeghalvad, Sepideh Shahkarami, et al.
Immunological Investigations|September 6, 2017
Interleukin-4 and Interleukin-10 Gene Polymorphisms in Patients with Inflammatory Bowel DiseaseNasser Ebrahimi Daryani, Amene Saghazadeh, Shirin Moossavi, et al.
Case Reports in Medicine|May 8, 2023
<i>DNAH11</i> and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the LiteratureFatemeh Sodeifian, Noosha Samieefar, Sepideh Shahkarami, et al.
Allergologia Et Immunopathologia|February 28, 2021
Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defectFateme Babaha, Reza Yazdani, Sepideh Shahkarami, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 18, 2021
Evaluation of MicroRNA-125b-5p and Transcription Factors BLIMP1 and IRF4 Expression in Unsolved Common Variable Immunodeficiency PatientsZahra Hamidi Esfahani, Reza Yazdani, Sepideh Shahkarami, et al.
Allergologia Et Immunopathologia|February 28, 2021
Novel <i>BTK</i> mutation in X-linked agammaglobulinemia: Report of a 17-year-old maleZoha Shaka, Helia Mojtabavi, Elham Rayzan, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Digestive Diseases and Sciences|December 4, 2014
Significance of IL-1RA Polymorphism in Iranian Patients with Inflammatory Bowel DiseaseNasser Ebrahimi Daryani, Maryam Sadr, Shirin Moossavi, et al.
Cell Journal|February 25, 2023
Minimal Residual Disease Detection Using Gene Scanning Analysis, Fluorescent Fragment Analysis, and Capillary Electrophoresis for IgH Rearrangement in Adult B-Lineage Acute Lymphoblastic Leukemia: A Cross-Sectional StudySepideh Shahkarami, Samareh Younesian, Shahrbano Rostami, et al.
Digestive Diseases (Basel, Switzerland)|August 23, 2018
Association of T Helper 1 Cytokine Gene Single Nucleotide Polymorphisms with Ulcerative Colitis and Crohn's DiseaseNasser Ebrahimi Daryani, Maryam Sadr, Samaneh Soltani, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 2, 2022
A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case ReportShaghayegh Sadeghmousavi, Sepideh Shahkarami, Elham Rayzan, et al.
Journal of Medical Case Reports|July 17, 2023
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothersElham Rayzan, Mona Sadeghalvad, Sepideh Shahkarami, et al.
Immunological Investigations|September 6, 2017
Interleukin-4 and Interleukin-10 Gene Polymorphisms in Patients with Inflammatory Bowel DiseaseNasser Ebrahimi Daryani, Amene Saghazadeh, Shirin Moossavi, et al.
Case Reports in Medicine|May 8, 2023
<i>DNAH11</i> and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the LiteratureFatemeh Sodeifian, Noosha Samieefar, Sepideh Shahkarami, et al.
Allergologia Et Immunopathologia|February 28, 2021
Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defectFateme Babaha, Reza Yazdani, Sepideh Shahkarami, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 18, 2021
Evaluation of MicroRNA-125b-5p and Transcription Factors BLIMP1 and IRF4 Expression in Unsolved Common Variable Immunodeficiency PatientsZahra Hamidi Esfahani, Reza Yazdani, Sepideh Shahkarami, et al.
Allergologia Et Immunopathologia|February 28, 2021
Novel <i>BTK</i> mutation in X-linked agammaglobulinemia: Report of a 17-year-old maleZoha Shaka, Helia Mojtabavi, Elham Rayzan, et al.
Pageof 4