| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ABO blood grouping and COVID-19: a hospital-based study in Eastern India
|
Behera, Birasen
|
|
|
23 |
1 |
|
artikel
|
| 2 |
A case–control study of BRCA1 founder mutations 185delAG and 5382insC in a cohort of Egyptian ovarian cancer patients using pyrosequencing technique
|
Rizk, Mohamed M.
|
|
|
23 |
1 |
|
artikel
|
| 3 |
A cost-effective method for detecting mutations in the human FAM111B gene associated with POIKTMP syndrome
|
Arowolo, Afolake
|
|
|
23 |
1 |
|
artikel
|
| 4 |
A genetic study of the association of six polymorphisms with rheumatoid arthritis in the Egyptian population
|
Ibrahim, Alaa M.
|
|
|
23 |
1 |
|
artikel
|
| 5 |
An actualized screening of schizophrenia-associated genes
|
Boulenouar, Houssam
|
|
|
23 |
1 |
|
artikel
|
| 6 |
Analysis of missense SNPs in the SLC47A1 and SLC47A2 genes affecting the pharmacokinetics of metformin: Computational approach
|
Avsar, Orcun
|
|
|
23 |
1 |
|
artikel
|
| 7 |
Analysis of real-time PCR Melanocortin 3 (MC3R) gene expression to identify new biomarkers inflammation in tuberculosis
|
Tenriola, Andi
|
|
|
23 |
1 |
|
artikel
|
| 8 |
A new case of trisomy 5 with complex karyotype abnormalities in B-cell prolymphocytic leukemia: a case study
|
Makongoro, Musa
|
|
|
23 |
1 |
|
artikel
|
| 9 |
A new insight into the diverse facets of microRNA-31 in oral squamous cell carcinoma
|
Kavitha, M.
|
|
|
23 |
1 |
|
artikel
|
| 10 |
An integration into the diagnostic workflow in a pediatric patient suspected of having Marfan syndrome
|
Oro, Maria
|
|
|
23 |
1 |
|
artikel
|
| 11 |
An investigation of 6-Shogaol effects on MCF7 cell lines through a systems biology approach
|
Amjad, Elham
|
|
|
23 |
1 |
|
artikel
|
| 12 |
A novel heterozygous TPM2 gene mutation (c.456G>C; p.Lys152Asn) in an Iranian family affected by distal arthrogryposis type 1: a case report
|
Neissi, Mostafa
|
|
|
23 |
1 |
|
artikel
|
| 13 |
A novel likely pathogenic variant in the H1-4 gene c.139G > C p.(Ala47Pro) associated with Rahman syndrome: a clinical report
|
González-Tarancón, R.
|
|
|
23 |
1 |
|
artikel
|
| 14 |
A novel variant luteinizing hormone receptor in the first transmembrane helix of two homozygous Iranian patients: case report
|
Sharif, Samaneh
|
|
|
23 |
1 |
|
artikel
|
| 15 |
A single-nucleotide polymorphism of IL12A gene (rs582537 A/C/G) and susceptibility to chronic hepatitis B virus infection among Iraqi patients
|
Mohsen, Rana T.
|
|
|
23 |
1 |
|
artikel
|
| 16 |
Association between single nucleotide polymorphism of human angiotensin-converting enzyme 2 gene locus and clinical severity of COVID-19
|
Elbadri, Shaimaa A.
|
|
|
23 |
1 |
|
artikel
|
| 17 |
Association of CAPN10 haplotype combinations with type 2 diabetes mellitus and metabolic syndrome among Egyptians: pilot study—genotyping of three CAPN10 variants
|
El-Far, Shaymaa W.
|
|
|
23 |
1 |
|
artikel
|
| 18 |
Association of CDKN2A/B gene polymorphisms (rs10811661 and rs2383208) with type 2 diabetes mellitus in a sample of Iraqi population
|
Fadheel, Hussein K.
|
|
|
23 |
1 |
|
artikel
|
| 19 |
Association of CHEK2 I157T and SULT1A1 R213H genetic variants with risk of sporadic colorectal cancer in a sample of Egyptian patients
|
Elhady, Ghada M.
|
|
|
23 |
1 |
|
artikel
|
| 20 |
Association of factor V Leiden R506Q, FXIIIVal34Leu, and MTHFR C677T polymorphisms with acute myocardial infarction
|
Golestani, Amin
|
|
|
23 |
1 |
|
artikel
|
| 21 |
Association of FTO gene variant rs9939609 with hyperandrogenemia and fasting glucose levels in South Indian women with polycystic ovarian syndrome
|
Naghshband, Zeinab
|
|
|
23 |
1 |
|
artikel
|
| 22 |
Association of FTO gene variants rs9939609 and rs1421085 with polycystic ovary syndrome
|
Alnafjan, Alaa A.
|
|
|
23 |
1 |
|
artikel
|
| 23 |
Association of gene polymorphisms of ACE, AGT, and ARNT-like protein 1 with susceptibility to gestational diabetes
|
Ashour, Esmat
|
|
|
23 |
1 |
|
artikel
|
| 24 |
Association of Interleukin 6 and Interleukin 8 genes polymorphisms with house dust mite-induced nasal-bronchial allergy in a sample of Indian patients
|
Dey, Debarati
|
|
|
23 |
1 |
|
artikel
|
| 25 |
Association of Keap1 (rs11085735) polymorphism and lncRNA MEG3 hypermethylation status with the risk of preeclampsia
|
Zangeneh, Maryam
|
|
|
23 |
1 |
|
artikel
|
| 26 |
Association of methylation status of ABCA1/G1 genes with the risk of coronary artery disease
|
Mansouri, Elaheh
|
|
|
23 |
1 |
|
artikel
|
| 27 |
Association of methyltetrahydrofolate reductase gene mutation, homocysteine level with semen quality of Iraqi infertile males
|
Al-janabi, Anwar Madlool
|
|
|
23 |
1 |
|
artikel
|
| 28 |
Association of OPRM1 with addiction: a review on drug, alcohol and smoking addiction in worldwide population
|
Hriatpuii, Vanlal
|
|
|
23 |
1 |
|
artikel
|
| 29 |
Association of primary knee osteoarthritis with DVWA SNP in a group of Egyptian population: a case–control study
|
Mostafa, Noha Abdelhady Abdelsadek
|
|
|
23 |
1 |
|
artikel
|
| 30 |
Association of the ANGPTL3 gene polymorphisms and haplotypes with cardiovascular diseases in Birjand longitudinal aging study (BLAS)
|
Poursalehi, Forough
|
|
|
23 |
1 |
|
artikel
|
| 31 |
A study of nasal epithelial cell gene expression in a sample of mild to severe asthmatic children and healthy controls
|
Behairy, Ola Galal Ali
|
|
|
23 |
1 |
|
artikel
|
| 32 |
A study of the genotyping and vascular endothelial growth factor polymorphism differences in diabetic and diabetic retinopathy patients
|
Wagih, Sara
|
|
|
23 |
1 |
|
artikel
|
| 33 |
A systems biology approach for investigating significantly expressed genes among COVID-19, hepatocellular carcinoma, and chronic hepatitis B
|
Sokouti, Babak
|
|
|
23 |
1 |
|
artikel
|
| 34 |
A Turkish case of incontinentia pigmenti with a deletion mutation at Inhibitor of kappa B kinase gamma gene
|
Ergin, Filiz Başak Cengiz
|
|
|
23 |
1 |
|
artikel
|
| 35 |
Autophagy-related genes in Egyptian patients with Behçet's disease
|
Saleh, Doaa N.
|
|
|
23 |
1 |
|
artikel
|
| 36 |
Becker congenital myotonia in black African with molecular findings
|
Azonbakin, Simon
|
|
|
23 |
1 |
|
artikel
|
| 37 |
Beta Thalassemia and Klinefelter syndrome: a rare occurrence
|
Billapati, Sushmitha
|
|
|
23 |
1 |
|
artikel
|
| 38 |
Biomarker potential of the GRP78 cell-free RNA in endometrial cancer
|
Aynekin, Busra
|
|
|
23 |
1 |
|
artikel
|
| 39 |
B2M gene knockout in HEK293T cells by non-viral delivery of CRISPR-Cas9 system for the generation of universal cells
|
Ranjbar, Maryam
|
|
|
23 |
1 |
|
artikel
|
| 40 |
Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene
|
Khairat, Rabab
|
|
|
23 |
1 |
|
artikel
|
| 41 |
BsmI gene polymorphism of vitamin D receptor in obese Egyptian male medical students and its relationship with vitamin D deficiency
|
Khattab, Yara
|
|
|
23 |
1 |
|
artikel
|
| 42 |
Cataloging the potential SNPs (single nucleotide polymorphisms) associated with quantitative traits, viz. BMI (body mass index), IQ (intelligence quotient) and BP (blood pressure): an updated review
|
Chauhan, Waseem
|
|
|
23 |
1 |
|
artikel
|
| 43 |
Cerebrospinal fluid biomarkers and genetic factors associated with normal pressure hydrocephalus and Alzheimer’s disease: a narrative review
|
Afrashteh, Fatemeh
|
|
|
23 |
1 |
|
artikel
|
| 44 |
Characterization of the expressed RNA variants from young patients with critical and non-critical SARS-CoV-2 infection
|
Okendo, Javan
|
|
|
23 |
1 |
|
artikel
|
| 45 |
Chronic myeloid leukemia: cytogenetics and molecular biology’s part in the comprehension and management of the pathology and treatment evolution
|
Benchikh, Sara
|
|
|
23 |
1 |
|
artikel
|
| 46 |
Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients
|
Abbassi, Meriame
|
|
|
23 |
1 |
|
artikel
|
| 47 |
Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds
|
Méndez-Rosado, Luis A.
|
|
|
23 |
1 |
|
artikel
|
| 48 |
Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery disease
|
Raza, Syed Tasleem
|
|
|
23 |
1 |
|
artikel
|
| 49 |
Clonal heterogeneity by fluorescence in situ hybridization in multiple myeloma: enhanced cytogenetic risk stratification
|
Abdel-Qader, Hadeel Yaseen
|
|
|
23 |
1 |
|
artikel
|
| 50 |
Comparative frequency distribution of glutathione S-transferase mu (GSTM1) and theta (GSTT1) allelic forms in Himachal Pradesh population
|
Hemlata,
|
|
|
23 |
1 |
|
artikel
|
| 51 |
Computational analysis of G-protein-coupled receptor kinase family members as potential targets for colorectal cancer therapy
|
Hermawan, Adam
|
|
|
23 |
1 |
|
artikel
|
| 52 |
Consanguinity in the Chaouia population (Morocco): prevalence, trends, determinants, fertility, and spontaneous abortions
|
Cheffi, Khadija
|
|
|
23 |
1 |
|
artikel
|
| 53 |
Co-overexpression of self-renewal markers SALL4 and HIWI is correlated with depth of tumor invasion and metastasis in colorectal cancer
|
Forghanifard, Mohammad Mahdi
|
|
|
23 |
1 |
|
artikel
|
| 54 |
Coronavirus-linked pregnancy complications: a comparative study
|
Gonlepa, Miapeh Kous
|
|
|
23 |
1 |
|
artikel
|
| 55 |
Correction: Autophagy-related genes in Egyptian patients with Behçet’s disease
|
Saleh, Doaa N.
|
|
|
23 |
1 |
|
artikel
|
| 56 |
Correction to: The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients
|
Mohamed, Rabab Afifi
|
|
|
23 |
1 |
|
artikel
|
| 57 |
Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report
|
Moudi, Mahdiyeh
|
|
|
23 |
1 |
|
artikel
|
| 58 |
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
|
Parisi, Giuseppe Fabio
|
|
|
23 |
1 |
|
artikel
|
| 59 |
Cytogenetic evaluation of primary amenorrhea: a study of 100 cases at tertiary centre
|
Pritti, Kumari
|
|
|
23 |
1 |
|
artikel
|
| 60 |
Decreased cell proliferation and induced apoptosis in human B-chronic lymphocytic leukemia following miR-221 inhibition through modulation of p27 expression
|
Ashrafi Dehkordi, Korosh
|
|
|
23 |
1 |
|
artikel
|
| 61 |
Design of a multi-epitope-based peptide vaccine against the S and N proteins of SARS-COV-2 using immunoinformatics approach
|
Rouzbahani, Arian Karimi
|
|
|
23 |
1 |
|
artikel
|
| 62 |
Detection of an FYCO1 nonsense mutation in an affected patient with autosomal recessive cataract (CTRCT18): a case report
|
Al-Badran, Raed Abdulelah
|
|
|
23 |
1 |
|
artikel
|
| 63 |
Detection of intestinal colonization by carbapenem-resistant Enterobacteriaceae (CRE) among patients admitted to a tertiary care hospital in Egypt
|
El-Defrawy, Inas
|
|
|
23 |
1 |
|
artikel
|
| 64 |
Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults
|
Khodarahmi, Mahdieh
|
|
|
23 |
1 |
|
artikel
|
| 65 |
Differential expression of microRNAs targeting genes associated with the development of high-grade gliomas
|
Kit, Oleg I.
|
|
|
23 |
1 |
|
artikel
|
| 66 |
Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail
|
Al-kuraishy, Hayder M.
|
|
|
23 |
1 |
|
artikel
|
| 67 |
Effect of virtual reality on motor coordination in children with cerebral palsy: a systematic review and meta-analysis of randomized controlled trials
|
Abdelhaleem, Naglaa
|
|
|
23 |
1 |
|
artikel
|
| 68 |
Evaluation of interleukin 10, interleukin 1-beta, and tumor necrosis factor-alpha gene polymorphisms in patients with periodontitis and healthy controls
|
Saremi, Leila
|
|
|
23 |
1 |
|
artikel
|
| 69 |
Evaluation of miRNA-21 and CA-125 as a promising diagnostic biomarker in patients with ovarian cancer
|
Talaat, Aliaa
|
|
|
23 |
1 |
|
artikel
|
| 70 |
Evaluation of the soldier's physical fitness test results (strength endurance) ın relation to genotype: longitudinal study
|
Yıldırım, Damla Selin
|
|
|
23 |
1 |
|
artikel
|
| 71 |
Exome sequencing identified a novel Col6α1 mutation in an Iranian patient with Ullrich congenital muscular dystrophy: a case report
|
Nekouei, Elaheh
|
|
|
23 |
1 |
|
artikel
|
| 72 |
Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report
|
Neissi, Mostafa
|
|
|
23 |
1 |
|
artikel
|
| 73 |
Explore the distribution of (rs35742686, rs3892097 and rs1065852) genetic polymorphisms of cytochrome P4502D6 gene in the Moroccan population
|
El Akil, Soumaya
|
|
|
23 |
1 |
|
artikel
|
| 74 |
Expression and diagnostic values of MIAT, H19, and NRON long non-coding RNAs in multiple sclerosis patients
|
Amiri, Mehrnoosh
|
|
|
23 |
1 |
|
artikel
|
| 75 |
Fibroblast growth factor-23 rs7955866 polymorphism and risk of chronic kidney disease
|
Ammar, Yaser Aly
|
|
|
23 |
1 |
|
artikel
|
| 76 |
Generation of muscle progenitors from human-induced pluripotent stem cells
|
Elmadbouh, Ibrahim
|
|
|
23 |
1 |
|
artikel
|
| 77 |
Genetic and molecular biology of gastric cancer among Iranian patients: an update
|
Abbaszadegan, Mohammad Reza
|
|
|
23 |
1 |
|
artikel
|
| 78 |
Genetic Counselling: the biomedical bridge between molecular diagnosis and precision treatment
|
Banerjee, Emili
|
|
|
23 |
1 |
|
artikel
|
| 79 |
Genetic diversity of Plasmodium falciparum isolates in Nigeria. A review
|
Opute, Augusta Onyebuchi
|
|
|
23 |
1 |
|
artikel
|
| 80 |
Genetic polymorphisms and gene expression of one-carbon metabolizing enzymes and their relation to breast cancer
|
Eldeeb, Mona Kamal
|
|
|
23 |
1 |
|
artikel
|
| 81 |
Genetics of type 2 diabetes mellitus in Indian and Global Population: A Review
|
Joseph, Anjaly
|
|
|
23 |
1 |
|
artikel
|
| 82 |
Genetic variation in toll-like receptor 4 gene with primary antiphospholipid syndrome susceptibility: a cohort of Egyptian patients
|
Mahdy, Sara H.
|
|
|
23 |
1 |
|
artikel
|
| 83 |
Hematological indices in pediatric patients with acyanotic congenital heart disease: a cross-sectional study of 248 patients
|
Mohammadi, Hanieh
|
|
|
23 |
1 |
|
artikel
|
| 84 |
Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy
|
Panwar, Deepak
|
|
|
23 |
1 |
|
artikel
|
| 85 |
Identifying the potential role of curcumin analogues as anti-breast cancer agents; an in silico approach
|
Praseetha, N. G.
|
|
|
23 |
1 |
|
artikel
|
| 86 |
Impact of gene polymorphism of glutathione S-transferase and ghrelin as a risk factor in Egyptian women with gestational diabetes mellitus
|
Madkour, Mai M.
|
|
|
23 |
1 |
|
artikel
|
| 87 |
Impact of IL-28B gene polymorphism on chronic hepatitis-C patients progression with diabetes and non-diabetes
|
Ateya, Rehab M.
|
|
|
23 |
1 |
|
artikel
|
| 88 |
Implication of single nucleotide polymorphisms in Interleukin-10 gene (rs1800896 and rs1800872) with severity of COVID-19
|
Rizvi, Saliha
|
|
|
23 |
1 |
|
artikel
|
| 89 |
Implications of mitochondrial DNA variants in pediatric B-cell acute lymphoblastic leukemia
|
Jain, Ayushi
|
|
|
23 |
1 |
|
artikel
|
| 90 |
Increased expression of IL-37 correlates with TNF-α levels and disease stage in endometriosis patients
|
Ragab, Dina
|
|
|
23 |
1 |
|
artikel
|
| 91 |
Influence of COVID-19 pandemic lockdown on a sample of Egyptian children with Down syndrome
|
Meguid, Nagwa A.
|
|
|
23 |
1 |
|
artikel
|
| 92 |
Influence of CYP2D6, CYP2C19 and CYP3A5 polymorphisms on plasma levels of tamoxifen metabolites in Algerian women with ER+ breast cancer
|
Boucenna, Amira
|
|
|
23 |
1 |
|
artikel
|
| 93 |
In silico analysis and the pathogenicity classification of PTS gene variants among Iranian population
|
Khamooshian, Sahand
|
|
|
23 |
1 |
|
artikel
|
| 94 |
In-silico analysis unravels the structural and functional consequences of non-synonymous SNPs in the human IL-10 gene
|
Das, Shuvo Chandra
|
|
|
23 |
1 |
|
artikel
|
| 95 |
In-silico characterization of phytochemicals identified from Vitex negundo (L) extract as potential therapy for Wnt-signaling proteins
|
Gouthami, Kuruvalli
|
|
|
23 |
1 |
|
artikel
|
| 96 |
In silico profiling of non-synonymous SNPs in IDS gene for early diagnosis of Hunter syndrome
|
Sivakumar, Adarshan
|
|
|
23 |
1 |
|
artikel
|
| 97 |
Intellectual developmental disorder with dysmorphic facies and ptosis caused by copy number variation including the BRPF1 gene in Peruvian patient
|
Abarca-Barriga, Hugo H.
|
|
|
23 |
1 |
|
artikel
|
| 98 |
Interactions dietary components with expression level of breast cancer-related genes
|
Bourbour, Fatemeh
|
|
|
23 |
1 |
|
artikel
|
| 99 |
Interleukin-4 gene intron 3 VNTR polymorphism in adult acute myeloid leukemia
|
Safwat, Nesma A.
|
|
|
23 |
1 |
|
artikel
|
| 100 |
Interleukin-1 receptor antagonist (IL-1RA) and interleukin-4 (IL-4) variable number of tandem repeat polymorphisms in schizophrenia and bipolar disorder: an association study in Turkish population
|
Pehlivan, Sacide
|
|
|
23 |
1 |
|
artikel
|
| 101 |
Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression
|
Hotkani, Maryam Mirzaei
|
|
|
23 |
1 |
|
artikel
|
| 102 |
Investigating expressed RNA variants that are related to disease severity in SARS-CoV-2-infected patients with mild-to-severe disease
|
Okendo, Javan
|
|
|
23 |
1 |
|
artikel
|
| 103 |
Investigating pathogenic SNPs in androgen receptor with direct influence on polycystic ovary syndrome (PCOS) in women
|
Ramadhan, Rehab S.
|
|
|
23 |
1 |
|
artikel
|
| 104 |
Investigation of miR-222 as a potential biomarker in diagnosis of patients with methamphetamine abuse disorder
|
Fathi, Shima
|
|
|
23 |
1 |
|
artikel
|
| 105 |
Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship
|
El-Amawy, Heba Saed
|
|
|
23 |
1 |
|
artikel
|
| 106 |
Mass spectrometry and two-dimensional electrophoresis in prenatal diagnosis of mucopolysaccharidosis type VI
|
Aboulnasr, Aly A.
|
|
|
23 |
1 |
|
artikel
|
| 107 |
Mendel paved the path toward understanding genetic diseases
|
Das, Sreejon Sundar
|
|
|
23 |
1 |
|
artikel
|
| 108 |
Methyltransferase-like 3 gene (METTL3) expression and prognostic impact in acute myeloid leukemia patients
|
Nagy, Reham Mohamed
|
|
|
23 |
1 |
|
artikel
|
| 109 |
MicroRNAs influence and longevity
|
Eshkoor, Sima Ataollahi
|
|
|
23 |
1 |
|
artikel
|
| 110 |
MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients
|
Hassan, Heba A.
|
|
|
23 |
1 |
|
artikel
|
| 111 |
Mobile phone radiation might alter gene expression in the oral squamous epithelial cells
|
Khalil, Ahmad M.
|
|
|
23 |
1 |
|
artikel
|
| 112 |
Momordica charantia nanoparticles potentiate insulin release and modulate antioxidant gene expression in pancreas of diabetic rats
|
Elekofehinti, Olusola Olalekan
|
|
|
23 |
1 |
|
artikel
|
| 113 |
Morbidity and mortality of COVID-19 negatively associated with the frequency of consanguineous marriages, an ecologic study
|
Saadat, Mostafa
|
|
|
23 |
1 |
|
artikel
|
| 114 |
MTHFR C677T (rs1801133) genetic polymorphism is associated with development risk of essential hypertension in the Turkish population
|
Er, Zafer Cengiz
|
|
|
23 |
1 |
|
artikel
|
| 115 |
Mutational analysis of phospholipase C epsilon 1 gene in Egyptian children with steroid-resistant nephrotic syndrome
|
Abdou, Mohammed
|
|
|
23 |
1 |
|
artikel
|
| 116 |
Myocardiocyte autophagy in the context of myocardiocytes regeneration: a potential novel therapeutic strategy
|
Marzoog, Basheer Abdullah
|
|
|
23 |
1 |
|
artikel
|
| 117 |
New heritable ATRX mutation identified by whole exome sequencing and review
|
Shahbazi, Zahra
|
|
|
23 |
1 |
|
artikel
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| 118 |
Oral cavity infection by the SARS-CoV-2: emphasizing the essence of masking and peptide therapeutics
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Ibiang, Glory Omini
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| 119 |
Orthopaedic interventions in occipital horn syndrome: a rare case of mutation in ATP7A gene
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Kaczmarek, Agata
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| 120 |
Pathway analysis of sepsis-induced changes gene expression
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Elbakkoush, Abdallah Ahmed
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| 121 |
Pathway analysis of smoking-induced changes in buccal mucosal gene expression
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Khaleel, Anas
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| 122 |
Polymorphism of the IL-10 gene in Azeri population of Iran
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Asgharzadeh, Mohammad
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| 123 |
Polymorphisms of nicotinic acetylcholine receptors in Alzheimer’s disease: a systematic review and data analysis
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Mohammadi, Solmaz
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| 124 |
Pre-microRNAs single nucleotide variants (rs3746444 A > G and rs2910164 C > G) increase the risk of ischemic stroke in the Egyptian population: a case–control study
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Abdelghany, Wafaa M.
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| 125 |
Prevalence and population genetic data of colour vision deficiency among students from selected tertiary institutions in Lagos State, Nigeria
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Fakorede, Samson Taiwo
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| 126 |
Problem of borderline hemoglobin A2 levels in an Iranian population with a high prevalence of α- and β-thalassemia carriers
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Moradi, Keivan
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| 127 |
Prognostic Potential of RDW in Discriminating Hemoglobinopathies among Patients reporting to Aga Khan Hospital, Kisumu
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Mutua, Benard
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| 128 |
P2X7 1513A/C loss-of-function polymorphism and active tuberculosis disease in a cohort of Egyptian population: a pilot study
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Shafiek, Hanaa
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| 129 |
Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
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Mohamed, Noura Mostafa
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| 130 |
Relation of the methylation state of RUNX3 and p16 gene promoters with hepatocellular carcinoma in Egyptian patients
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El-shaarawy, Fatma
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| 131 |
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Poudel, Phanindra Prasad
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| 132 |
Role of eNOS and TGFβ1 gene polymorphisms in the development of diabetic nephropathy in type 2 diabetic patients in South Indian population
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Varghese, Sindhu
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| 133 |
Role of microRNAs in regulation of WNT signaling pathway in urothelial and prostate cancers
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Montazer, Mehdi
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| 134 |
SARS-CoV-2 origin, myths and diagnostic technology developments
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Wambani, Josephine
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| 135 |
Secure framework for IoT technology based on RSA and DNA cryptography
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Elamir, Mona M.
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| 136 |
Selection hub MicroRNAs as biomarkers in breast cancer stem cells in extracellular matrix using bioinformatics analyses
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Shirinsokhan, Armaghan
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| 137 |
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Saleh, Dina Amin
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| 138 |
Significance of promoter methylation of multiple tumor suppressor genes in hepatocellular carcinoma
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Tahoon, Alaa
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| 139 |
SMA carrier testing using Real-time PCR as a potential preconception screening tool
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Eissa, Noura Raafat
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| 140 |
Spectrum of MEFV gene mutations in 4,256 familial Mediterranean fever patients from Iran: a comprehensive systematic review
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Alibakhshi, Reza
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1 |
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| 141 |
Study of the association between GLIS3 rs10758593 and type 2 diabetes mellitus in Egyptian population
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Farid, Mai Mohamed Mohamed
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| 142 |
Targeted next generation sequencing provides insight for the genetic alterations in liquid biopsy of Egyptian brain tumor patients
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Kassem, Neemat M.
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| 143 |
Telomere attrition and inflammation: the chicken and the egg story
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Niveta, J. P. Shirley
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| 144 |
The association between variant rs9939609 in the FTO gene with free leptin index and the risk of obesity in the Indonesian children population
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Lubis, Siska Mayasari
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1 |
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| 145 |
The correlation between P53 and COX-2 expression and the pathological alteration in hepatocellular carcinoma
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Sakr, Moustafa A.
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1 |
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| 146 |
The efficacy of clopidogrel in preventing recurrent cardiovascular events among Arab population carrying different CYP2C19 mutations: systematic review and meta-analysis
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Alkattan, Abdullah N.
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| 147 |
The first combined meta‐analytic approach for elucidating the relationship of circulating resistin levels and RETN gene polymorphisms with colorectal and breast cancer
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Aziz, Md. Abdul
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23 |
1 |
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| 148 |
The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients
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Mohamed, Rabab Afifi
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23 |
1 |
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| 149 |
The HLA profile and genetic affinities of three primitive Tamil-speaking endogamous groups: Kallars of Thanjavur, Piramalai Kallar and Vanniyar
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Raju, Kamaraj
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1 |
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| 150 |
The potential application of probiotics for the prevention and treatment of COVID-19
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Elekhnawy, Engy
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| 151 |
The role of angiotensin-converting enzyme 2 (ACE2) genetic variations in COVID-19 infection: a literature review
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Fawzy, Manal S.
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| 152 |
The role of radiogenomics in the diagnosis of breast cancer: a systematic review
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Darvish, Leili
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| 153 |
The role of tumor necrosis factor alpha − 308A > G polymorphism on the clinical states of SARS-CoV-2 infection
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Sotomayor-Lugo, Francisco
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| 154 |
The synergistic effect of eucalyptus oil and retinoic acid on human esophagus cancer cell line SK-GT-4
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Falih, Saba M. J.
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| 155 |
Three novel variants in SOX10 gene: Waardenburg and PCWH syndromes
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Sienes Bailo, Paula
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| 156 |
Three uncommon mutations of the SLC12A3 gene in gitelman syndrome: case reports and review of the literature
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Akpinar Gozetici, Melis
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|
| 157 |
TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global population
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Mohd Atan, Farah Nur Elina
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| 158 |
TMPRSS6 rs855791 polymorphism is associated with iron deficiency in a cohort of Sri Lankan pregnant women
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Abeywickrama, Halinne Lokuge Thilakshi Chamanika
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| 159 |
Toll-like receptor 10 gene polymorphism and risk of multiple sclerosis among Iraqi patients
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Atiyah, Noor S.
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| 160 |
Understanding the pivotal roles of ACE2 in SARS-CoV-2 infection: from structure/function to therapeutic implication
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Pouremamali, Amir
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| 161 |
Use of multiplex PCR in diagnosis of childhood acute viral diarrhoea caused by rotavirus, norovirus, astrovirus and adenovirus in Upper Egypt
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Othma, Amr Abulhamd Sayed
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| 162 |
Validated establishment of anthropometric measurements of mid-face zone in Egyptian healthy preschool-age children: a cross-sectional study
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El Ella, Soheir S. Abou
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| 163 |
Vascular endothelial growth factor A with two genetic variants for prediction of mixed microvascular diabetic complications
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Omar, Thoria Ahmed
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| 164 |
Virtual screening and molecular dynamic simulations of the antimalarial derivatives of 2-anilino 4-amino substituted quinazolines docked against a Pf-DHODH protein target
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Ibrahim, Zakari Ya’u
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| 165 |
Vitamin D receptor gene polymorphism in Madura pregnant women with hypertension: a case control study
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Setiarsih, Dini
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| 166 |
Von Hippel–Lindau (VHL) disease and VHL-associated tumors in Indian subjects: VHL gene testing in a resource constraint setting
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Dwivedi, Aradhana
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| 167 |
Wilms tumor 1 gene expression in acute myeloid leukemia: prognostic significance and usefulness in minimal residual disease monitoring—a case–control study
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Donia, Hanaa Mahmoud
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