Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients-Reference-Cited by-同舟云学术

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Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients

Published:2019-09-03 Issue:4-5 Volume:43 Page:258-263
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

El Sissy Maha H.¹,Hafez Ahmed A.¹,Moneim Sherif E.A.²,Eldemerdash Doaa M.³

Affiliation:

1. Department of Laboratory Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt;

2. Department of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt;

3. Department of Internal Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1680381

Reference37 articles.

1. Molecular Cloning and Functional Expression of a Novel CC Chemokine Receptor cDNA from a Human Basophilic Cell Line

2. Seven-transmembrane receptors

3. Chemokine receptor CCR5: insights into structure, function, and regulation

4. Chemokines and Chemokine Receptors: Positioning Cells for Host Defense and Immunity

5. Guide to Receptors and Channels (GRAC), 3rd edition

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of biomarkers and pathways for focal segmental glomerulosclerosis using next generation sequencing data and bioinformatics analysis;2022-06-10

2. CCR5Δ32 in Brazil: Impacts of a European Genetic Variant on a Highly Admixed Population;Frontiers in Immunology;2021-12-10

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