جامعة أم القرى

جامعة أم القرى

السيرة الذاتية  ناصر الهواري

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ناصر عطية حامد الهواري

أستاذ

قسم علم الوراثة الطبية - كلية الطب

كلية الطب

تواصل

 

المؤهلات

الدكتوراه

‏العلوم الطبية الأساسية

اسم جهة التخرج جامعة عين شمس

البلد جمهورية مصر

البلد 2000

الماجستير

البرامج العامة والمؤهلات غير محددة أكثر

اسم جهة التخرج جامعة عين شمس

البلد جمهورية مصر

البلد 1991

البكالوريوس

‏الكيمياء

اسم جهة التخرج جامعة القاهرة

البلد جمهورية مصر

البلد 1982

الأبحاث العلمية

Trimetazidine Alleviates Bleomycin-Induced Pulmonary Fibrosis by Targeting the Long Noncoding RNA CBR3-AS1-Mediated miRNA-29 and Resistin-Like Molecule alpha 1: Deciphering a Novel Trifecta Role of LncRNA CBR3-AS1/miRNA-29/FIZZ1 Axis in Lung Fibrosis

مقال في مجلة

DOVE Press, Drug Design, Development and Therapy, 2024

Clinical Epidemiology and APOE Gene Etiology: An Update on Alzheimer’s Disease

مقال في مجلة

URF publishers, Medical & Clinical Case Reports Journal, 2024

Deciphering the therapeutic potential of trimetazidine in rheumatoid arthritis via targeting mi-RNA128a, TLR4 signaling pathway, and adenosine-induced FADD-microvesicular shedding: In vivo and in silico study

مقال في مجلة

Lausanne-Frontiers Media, Frontiers in Pharmacology, 2024

Prospective Functions of miRNA Variants May Predict Breast Cancer Among Saudi Females

مقال في مجلة

Palo Alto, CA : Cureus, Inc, Cureus, 2023

Phenotypic variability to medication management: an update on fragile X syndrome

مقال في مجلة

BMC-Springer Nature, Human Genomics, 2023

Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma

مقال في مجلة

Palo Alto, CA : Cureus, Inc, Cureus, Journal of Medical Science, 2023

Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community

مقال في مجلة

DovePress, International Journal of General Medicine, 2021

Genetic etiology and clinical challenges of phenylketonuria

مقال في مجلة

Springer Nature, Human Genomics, 2022

NPHS1 and NPHS2 variants associated with early-onset frequently relapsing or steroid-dependent nephrotic syndrome in the Saudi community

مقال في مجلة

IRIS Publishers, Annals of Urology and Nephrology, 2022

Methylenetetrahydrofolate Reductase Gene and Potential Risk to Autism Spectrum Disorder

مقال في مجلة

B P International, New Horizons in Medicine and Medical Research, 2022

Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community

مقال في مجلة

DOVE Medical Press Inc, International Journal of General Medicine, 2021

Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

مقال في مجلة

Elsevier, Egyptian Journal of Medical Human Genetics, 2011

Association between ANKK1 (rs1800497) and LTA (rs909253) Genetic Variants and Risk of Schizophrenia

مقال في مجلة

Hindawi Pub. Co, BioMed Research International, 2015

Risk of Colorectal Carcinoma May Predispose to the Genetic Variants of the GST, CYP450, and TP53 Genes among nonsmokers in the Saudi Community

مقال في مجلة

DOVE Medical Press Inc, International Journal of General Medicine, 2021

Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population

مقال في مجلة

Hindawi Pub. Co, Disease Markers, 2014

Common Tag STSs in the AZF Region Associated with Azoospermia and Severe Oligospermia in Infertile Egyptian Men

مقال في مجلة

Benthamopen Inc, The Open Andrology Journal, 2010

Azoospermia factor microdeletions: common tag STSs in infertile men with azoospermia and sever oligospermia from Egypt

مقال في مجلة

BioMed Central, BMC Genomics, 2014

TNF -238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population

مقال في مجلة

Wiley, Pediatric Pulmonology, 2013

Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria

مقال في مجلة

SAP-Slovak Academic Press, Bratislav Medical Journal, 2008

Molecular updating of beta-thalassemia mutations in Upper Egyptian population

مقال في مجلة

Taylor and Francis online, Hemoglobin, 2010

Association between beta+252 tumour necrosis factor polymorphism and asthma in western Saudi children

مقال في مجلة

Elsevier, Saudi Journal of Biological Sciences, 2011

Frameshift deletion mechanisms with Duchenne and Becker muscular dystrophy in Egyptian families

مقال في مجلة

Korean Society for Molecular Biology, Molecules and Cells, 2004

The impact of common tumor necrosis factor haplotypes on the development of asthma in children: an Egyptian model

مقال في مجلة

Marry Ann Liebert Inc. Publisher, Genetic Testing and Molecular Biomarkers, 2011

High precision DNA microsatellite genotyping in Duchenne muscular dystrophy families using ion-pair reversed-phase high performance liquid chromatography

مقال في مجلة

ScienceDirect, Clinical Biochemistry, 2006

Mutations in transglutaminase gene 1 in autosomal recessive congenital lamellar ichthyosis in Egyptian families

مقال في مجلة

Chichester ; New York : Wiley, Disease Markers, 2005

Polymorphisms of TAP1/LMP7 loci in Egyptian patients with vitiligo

مقال في مجلة

Ain Shams University Press, Egyptian Journal of Medical Human Genetics, 2006

The MTHFR 677T allele may influence the severity and biochemical risk factors of Alzheimer's disease in an Egyptian population

مقال في مجلة

Hindawi Pub. Co, Disease Markers, 2013

الكتب

New Horizons in Medicine and Medical Research

2022

Beta-thal mutations in Middle East

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Beta-Globin Gene Mutations

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Single Nucleotide Substitution in Multifactorial Disorders

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جار التحميل