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  • 1-10 ل  15 نتائج ل ""Universal""

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Publication : immunological investigations Language : bulgarian Language : danish Language : english Language : gothic Language : interlingua (international auxiliary language association) Language : macedonian Language : multiple languages Language : nepal bhasa Language : slovenian Language : welsh Language : western frisian فلترة بواسطة : مؤلف
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Academic Journal

Study of NLRP3 Single Nucleotide Polymorphisms in Juvenile Systemic Lupus Erythematosus (JSLE).

  • Authors : Yazdanpanah N; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.

Subjects: Genetic Predisposition to Disease* ; Lupus Erythematosus, Systemic*/Lupus Erythematosus, Systemic*/Lupus Erythematosus, Systemic*/genetics; Humans

  • Source: Immunological investigations [Immunol Invest] 2023 Nov; Vol. 52 (5), pp. 598-615. Date of Electronic Publication: 2023 Jun 01.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The Overlap between Genetic Susceptibility to COVID-19 and Skin Diseases.

  • Authors : Jabalameli N; Network of Dermatology Research (NDR), Universal Scientific Education and Research Network (USERN), Tehran, Iran.; Rajabi F

Subjects: COVID-19*/COVID-19*/COVID-19*/genetics ; Exodeoxyribonucleases*/Exodeoxyribonucleases*/Exodeoxyribonucleases*/genetics ; Phosphoproteins*/Phosphoproteins*/Phosphoproteins*/genetics

  • Source: Immunological investigations [Immunol Invest] 2022 May; Vol. 51 (4), pp. 1087-1094. Date of Electronic Publication: 2021 Jan 26.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS).

  • Authors : Fekrvand S; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Science, Tehran, Iran.; Delavari S

Subjects: Immunologic Deficiency Syndromes*/Immunologic Deficiency Syndromes*/Immunologic Deficiency Syndromes*/genetics ; Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/genetics; Child

  • Source: Immunological investigations [Immunol Invest] 2022 Apr; Vol. 51 (3), pp. 644-659. Date of Electronic Publication: 2021 Jan 06.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Evaluation of Expression of LRBA and CTLA-4 Proteins in Common Variable Immunodeficiency Patients.

  • Authors : Salami F; Reproductive Immunology Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.

Subjects: Common Variable Immunodeficiency*/Common Variable Immunodeficiency*/Common Variable Immunodeficiency*/diagnosis ; Common Variable Immunodeficiency*/Common Variable Immunodeficiency*/Common Variable Immunodeficiency*/genetics; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/genetics

  • Source: Immunological investigations [Immunol Invest] 2022 Feb; Vol. 51 (2), pp. 381-394. Date of Electronic Publication: 2020 Nov 15.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Wharton's Jelly Mesenchymal Stem Cells Exosomes and Conditioned Media Increased Neutrophil Lifespan and Phagocytosis Capacity.

Subjects: Exosomes* ; Mesenchymal Stem Cells* ; Wharton Jelly*

  • Source: Immunological investigations [Immunol Invest] 2021 Nov; Vol. 50 (8), pp. 1042-1057. Date of Electronic Publication: 2020 Aug 11.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR).

  • Authors : Rahmani F; Department of Radiology, Washington University School of Medicine, St Louis, Missouri, USA.; Student's Scientific Research Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

Subjects: Inflammatory Bowel Diseases/Inflammatory Bowel Diseases/Inflammatory Bowel Diseases/*genetics ; Primary Immunodeficiency Diseases/Primary Immunodeficiency Diseases/Primary Immunodeficiency Diseases/*genetics; Child, Preschool

  • Source: Immunological investigations [Immunol Invest] 2021 May; Vol. 50 (4), pp. 445-459. Date of Electronic Publication: 2020 Jul 07.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Identifying Novel Mutations in Iranian Patients with LPS-responsive Beige-like Anchor Protein (LRBA) Deficiency.

  • Authors : Ghaini M; Immunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran.; Arzanian MT

Subjects: Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*deficiency ; Immunologic Deficiency Syndromes/Immunologic Deficiency Syndromes/Immunologic Deficiency Syndromes/*genetics; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/genetics

  • Source: Immunological investigations [Immunol Invest] 2021 May; Vol. 50 (4), pp. 399-405. Date of Electronic Publication: 2020 Jun 01.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Effect of Class Switch Recombination Defect on the Phenotype of Ataxia-Telangiectasia Patients.

  • Authors : Amirifar P; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences , Tehran, Iran.; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, University of Medical Science , Tehran, Iran.

Subjects: Ataxia Telangiectasia/Ataxia Telangiectasia/Ataxia Telangiectasia/*epidemiology ; Immunologic Deficiency Syndromes/Immunologic Deficiency Syndromes/Immunologic Deficiency Syndromes/*epidemiology ; Respiratory Tract Infections/Respiratory Tract Infections/Respiratory Tract Infections/*epidemiology

  • Source: Immunological investigations [Immunol Invest] 2021 Feb; Vol. 50 (2-3), pp. 201-215. Date of Electronic Publication: 2020 Mar 02.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Disturbed Transcription of TLRs' Negative Regulators and Cytokines Secretion among TLR4- and 9-Activated PBMCs of Agammaglobulinemic Patients.

  • Authors : Sanaei R; Immunology Research Center (IRC), Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences , Tehran , Iran.; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN) , Tehran , Iran.

Subjects: Agammaglobulinemia/Agammaglobulinemia/Agammaglobulinemia/*metabolism ; Cytokines/Cytokines/Cytokines/*metabolism ; Leukocytes, Mononuclear/Leukocytes, Mononuclear/Leukocytes, Mononuclear/*metabolism

  • Source: Immunological investigations [Immunol Invest] 2019 Nov; Vol. 48 (8), pp. 860-874. Date of Electronic Publication: 2019 Jun 11.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The Association between Genetic Variation in Wnt Transcription Factor TCF7L2 ( TCF4 ) and Alopecia Areata.

  • Authors : Rajabi F; a Skin Research Center , Shahid Beheshti University of Medical Sciences , Tehran , Iran.; b Network of Dermatology Research (NDR) , Universal Scientific Education and Research Network (USERN) , Tehran , Iran.

Subjects: Genotype*; Alopecia Areata/Alopecia Areata/Alopecia Areata/*genetics ; Transcription Factor 7-Like 2 Protein/Transcription Factor 7-Like 2 Protein/Transcription Factor 7-Like 2 Protein/*genetics

  • Source: Immunological investigations [Immunol Invest] 2019 Aug; Vol. 48 (6), pp. 555-562. Date of Electronic Publication: 2019 Apr 23.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8504629 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 ل  15 نتائج ل ""Universal""