| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of spastic paraplegia type 11 with a variation in the SPG11 gene
|
Elmas, Muhsin
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21 |
1 |
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artikel
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| 2 |
A high mannose concentration is well tolerated by colorectal adenocarcinoma and melanoma cells but toxic to normal human gingival fibroblast: an in vitro investigation
|
Mazlan, Muhammad Alif
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21 |
1 |
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artikel
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| 3 |
Angiotensin-converting enzyme insertion/deletion (I/D) gene polymorphism in Iraqi type 2 diabetic patients: association with the risk of cardiac autonomic neuropathy
|
Dhumad, Muhanad M.
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21 |
1 |
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artikel
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| 4 |
An in silico epitope-based peptide vaccine design against the 2019-nCoV
|
Durojaye, Olanrewaju Ayodeji
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21 |
1 |
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artikel
|
| 5 |
An in silico LLPS perturbation approach in the design of a novel SARS-CoV-2 spike receptor-binding domain inhibitor
|
Durojaye, Olanrewaju Ayodeji
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21 |
1 |
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artikel
|
| 6 |
A novel mutation in ITGB4 gene in a newborn with epidermolysis bullosa, pyloric atresia, and aplasia cutis congenita
|
Okulu, Emel
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21 |
1 |
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artikel
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| 7 |
Assessment of vitamin D-binding protein (DBP) gene polymorphisms and their correlation with multiple sclerosis: a case-control study in a sample of the Syrian population
|
Alhomsi, Bushra
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21 |
1 |
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artikel
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| 8 |
Association between ABO blood groups and susceptibility to COVID-19: profile of age and gender in Iraqi patients
|
Ad’hiah, Ali H.
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21 |
1 |
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artikel
|
| 9 |
Association between calcium-sensing receptor (CaSR) R990G, CaSR A986S, and CaSR Q1011E gene polymorphisms and the risk of urolithiasis: a meta-analysis
|
Daryanto, Besut
|
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21 |
1 |
p. 1-12
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artikel
|
| 10 |
Association between genetic polymorphism of XRCC7 (G6721T) and risk of acute lymphoblastic leukemia
|
Farokhian, Farnoush
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21 |
1 |
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artikel
|
| 11 |
Association between genetic polymorphism of XRCC6 T-991C and risk of varicocele
|
Namvaran, Mohammad Reza
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21 |
1 |
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artikel
|
| 12 |
Case report: Pitt-Hopkins like syndrome with CNTNAP2 mutation
|
AlBaazi, Sawsan
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21 |
1 |
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artikel
|
| 13 |
Characterization of the major human STAG3 variants using some proteomics and bioinformatics assays
|
Lafta, Inam J.
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21 |
1 |
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artikel
|
| 14 |
Clinical impact of early minimal residual disease detection at day 15 in precursor B-childhood acute lymphoblastic leukemia: an Egyptian experience
|
Farweez, Botheina Ahmed Thabet
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21 |
1 |
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artikel
|
| 15 |
COL1A1 polymorphism and neurological complications in pediatric acute lymphoblastic leukemia patients and their associations with altered bone mineral density
|
Omran, Alaa A.
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21 |
1 |
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artikel
|
| 16 |
Computational evaluation of potent 2-(1H-imidazol-2-yl) pyridine derivatives as potential V600E-BRAF inhibitors
|
Umar, Abdullahi Bello
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21 |
1 |
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artikel
|
| 17 |
Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways
|
Suluba, Emmanuel
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21 |
1 |
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artikel
|
| 18 |
Contributory role of SARS-CoV-2 genomic variations and life expectancy in COVID-19 transmission and low fatality rate in Africa
|
Omotoso, Olabode E.
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21 |
1 |
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artikel
|
| 19 |
COVID-19 susceptibility: potential of ACE2 polymorphisms
|
Chaudhary, Mayank
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21 |
1 |
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artikel
|
| 20 |
Detection of tmprss2-erg and tmprss2-egr1 gene fusion in prostate cancer from a Chinese population
|
Xu, Changqing
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21 |
1 |
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artikel
|
| 21 |
Development of a simple method for the analysis of phenylalanine in dried blood spot using tandem mass spectrometry
|
Gouda, Amr S.
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21 |
1 |
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artikel
|
| 22 |
DNA integrity index as a potential molecular biomarker in colorectal cancer
|
Salem, Ramy
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21 |
1 |
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artikel
|
| 23 |
Double aneuploidy 48,ХХХ,+21 of a Bulgarian newborn with Down phenotype: a case report
|
Tsvetkova, Mariya
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|
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21 |
1 |
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artikel
|
| 24 |
Effect of folic acid on animal models, cell cultures, and human oral clefts: a literature review
|
Bendahan, Zita C.
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|
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21 |
1 |
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artikel
|
| 25 |
Evaluating of the association between ABO blood groups and coronavirus disease 2019 (COVID-19) in Iraqi patients
|
Ad’hiah, Ali H.
|
|
|
21 |
1 |
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artikel
|
| 26 |
Evaluation of CD147 gene expression, lipid peroxidation, and antioxidants in cases of acute coronary syndrome in Egyptian population
|
Emam, Wafaa A.
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|
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21 |
1 |
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artikel
|
| 27 |
Evaluation of glutathione S-transferase polymorphism in Iranian patients with type 2 diabetic microangiopathy
|
Hashemi-Soteh, Mohammad Bagher
|
|
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21 |
1 |
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artikel
|
| 28 |
Evaluation of the clinical value of circulating miR-101, miR-187 and miR-21 in neonatal sepsis diagnosis and prognosis
|
Salim, Rabab F.
|
|
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21 |
1 |
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artikel
|
| 29 |
Exploring the multiple roles of guardian of the genome: P53
|
Feroz, Wasim
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|
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21 |
1 |
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artikel
|
| 30 |
Expression of miR-146a and miR-155 in Egyptian patients with Behçet’s disease: clinical significance and relationship with disease activity
|
El Khateeb, Engy
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|
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21 |
1 |
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artikel
|
| 31 |
Extended blood group profiles for Malays, Chinese, and Indians in Peninsular Malaysia
|
Hajar, Che Ghazali Norul
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|
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21 |
1 |
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artikel
|
| 32 |
Genes predisposing to syndromic and nonsyndromic infertility: a narrative review
|
Yahaya, Tajudeen O.
|
|
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21 |
1 |
|
artikel
|
| 33 |
Genotype association of IP6K3 gene with Hashimoto’s thyroiditis in Algerian population (Aures region)
|
Kherrour, Warda
|
|
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21 |
1 |
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artikel
|
| 34 |
Hematological and demographic profile of Pakistani children with isolated ventricular septal defects (VSDs)
|
Sarwar, Sumbal
|
|
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21 |
1 |
|
artikel
|
| 35 |
Hepatoprotective effect of Moringa oleifera extract on TNF-α and TGF-β expression in acetaminophen-induced liver fibrosis in rats
|
Aly, Omnia
|
|
|
21 |
1 |
|
artikel
|
| 36 |
Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism
|
Agarwala, Swati
|
|
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21 |
1 |
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artikel
|
| 37 |
Inflammation-related gene polymorphisms associated with Parkinson’s disease: an updated meta-analysis
|
Ulhaq, Zulvikar Syambani
|
|
|
21 |
1 |
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artikel
|
| 38 |
Inherited thrombophilia and recurrent pregnancy loss: a single-center case-control study in North-Western Algeria
|
Nassour-Mokhtari, Ilhem
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|
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21 |
1 |
|
artikel
|
| 39 |
In silico analysis of non-synonymous single nucleotide polymorphisms of human DEFB1 gene
|
Venkata Subbiah, Harini
|
|
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21 |
1 |
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artikel
|
| 40 |
Integrative analysis of mRNA and miRNA sequencing data for gliomas of various grades
|
Gvaldin, Dmitry Y.
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|
|
21 |
1 |
|
artikel
|
| 41 |
Lack of association between three common genetic variations of XPC and susceptibility to age-related macular degeneration, a preliminary study
|
Kalteh, Sharareh
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|
|
21 |
1 |
|
artikel
|
| 42 |
Late-onset multiple acyl-CoA dehydrogenase deficiency with breast cancer
|
Pavithran, Keechilat
|
|
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21 |
1 |
|
artikel
|
| 43 |
Long non-coding RNA HOTAIR and HOTTIP as potential biomarkers for hepatitis C virus genotype 4-induced hepatocellular carcinoma
|
Roshdy, Fawzy
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|
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21 |
1 |
|
artikel
|
| 44 |
Low iron mitigates viral survival: insights from evolution, genetics, and pandemics—a review of current hypothesis
|
Menshawey, Rahma
|
|
|
21 |
1 |
|
artikel
|
| 45 |
Lymphoid enhancer-binding factor 1 (LEF-1): a favorable prognostic factor in adult acute myeloid leukemia in Egyptian patients
|
Farweez, Botheina Ahmed Thabet
|
|
|
21 |
1 |
|
artikel
|
| 46 |
Lysinuric protein intolerance: an overlooked diagnosis
|
Olgac, Asburce
|
|
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21 |
1 |
|
artikel
|
| 47 |
Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age
|
El Bouchikhi, Ihssane
|
|
|
21 |
1 |
|
artikel
|
| 48 |
Novel mutation in perforin gene causing familial hemophagocytic lymphohistiocytosis type 2 in an Egyptian infant: case report
|
Almalky, Mohamed
|
|
|
21 |
1 |
|
artikel
|
| 49 |
Potential therapeutic target identification in the novel 2019 coronavirus: insight from homology modeling and blind docking study
|
Durojaye, Olanrewaju Ayodeji
|
|
|
21 |
1 |
|
artikel
|
| 50 |
Prediction and in silico validation of MYH7 gene missense variants in the Iranian population: a bioinformatics analysis based on Iranome database
|
Shahbazi, Shirin
|
|
|
21 |
1 |
|
artikel
|
| 51 |
Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype
|
El-Dessouky, Sara H.
|
|
|
21 |
1 |
|
artikel
|
| 52 |
Prognostic significance of DNMT3a gene expression and reactive nitrogen species in newly diagnosed Egyptian de novo adult acute myeloid leukemia patients
|
Asfour, Inas A.
|
|
|
21 |
1 |
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artikel
|
| 53 |
Prognostic value of CIP2A gene expression in adult Egyptian acute myeloid leukemia patients
|
Shafik, Roxan E.
|
|
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21 |
1 |
|
artikel
|
| 54 |
Purinergic signalling pathway: therapeutic target in ovarian cancer
|
Chandran, Nisha
|
|
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21 |
1 |
|
artikel
|
| 55 |
Reductive regulation of BECN1 gene in adult Egyptian patients with do novo AML
|
Ghozlan, Manal Fawzy
|
|
|
21 |
1 |
|
artikel
|
| 56 |
Role of interleukins 12B and 17A genetic variation in house dust mites allergy
|
Ammar, Asmaa Mostafa
|
|
|
21 |
1 |
|
artikel
|
| 57 |
Role of mesenchymal stem cells and their culture medium in alleviating kidney injury in rats diabetic nephropathy
|
Ibrahim, Amal Al-Shahat
|
|
|
21 |
1 |
|
artikel
|
| 58 |
Role of phototherapy, BAX gene expression in hyperbilirubinemia development in full-term neonates
|
Afifi, Mohamed farouk
|
|
|
21 |
1 |
|
artikel
|
| 59 |
Role of swimming on muscle PGC-1α, FNDC5 mRNA, and assessment of serum omentin, adropin, and irisin in high carbohydrate high fat (HCHF) diet induced obesity in rats
|
Badawy, Ehsan
|
|
|
21 |
1 |
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artikel
|
| 60 |
Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature
|
Eid, Ola M.
|
|
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21 |
1 |
|
artikel
|
| 61 |
SHOX2 gene methylation in Egyptians having lung cancer
|
Rizk, Mohamed Mostafa Mohamed Ahmed
|
|
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21 |
1 |
|
artikel
|
| 62 |
Spinal muscular atrophy in Venezuela: quantitative analysis of SMN1 and SMN2 genes
|
Yépez, Yuri
|
|
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21 |
1 |
|
artikel
|
| 63 |
Strategies to target long non-coding RNAs in cancer treatment: progress and challenges
|
Fathi Dizaji, Behdokht
|
|
|
21 |
1 |
|
artikel
|
| 64 |
Structure-based design of some quinazoline derivatives as epidermal growth factor receptor inhibitors
|
Ibrahim, Muhammad Tukur
|
|
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21 |
1 |
|
artikel
|
| 65 |
Susceptibility role of soluble HLA-G and HLA-G 14-bp insertion/deletion polymorphism in inflammatory bowel disease
|
Abdul-Hussein, Sarah S.
|
|
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21 |
1 |
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artikel
|
| 66 |
The association between toll-like receptor 4 (TLR4) genotyping and the risk of epilepsy in children
|
Abdelsalam, Maha
|
|
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21 |
1 |
|
artikel
|
| 67 |
The associations among RARRES2 rs17173608 gene polymorphism, serum chemerin, and non-traditional lipid profile in patients with metabolic syndrome
|
Dahpy, Marwa A.
|
|
|
21 |
1 |
|
artikel
|
| 68 |
The morbidity and mortality of COVID-19 are correlated with the Ile105Val glutathione S-transferase P1 polymorphism
|
Saadat, Mostafa
|
|
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21 |
1 |
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artikel
|
| 69 |
Understanding the genetic determinant of severity in viral diseases: a case of SARS-Cov-2 infection
|
Oladejo, Babayemi Olawale
|
|
|
21 |
1 |
|
artikel
|
| 70 |
Update on the genetic and epigenetic etiology of gestational diabetes mellitus: a review
|
Yahaya, Tajudeen O.
|
|
|
21 |
1 |
|
artikel
|
| 71 |
Vici syndrome in an Egyptian infant: case report and differential diagnosis of inherited hypopigmented disorders
|
Abd Elmaksoud, Marwa
|
|
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21 |
1 |
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artikel
|
| 72 |
Vitamin D receptor (VDR) gene FokI, BsmI, ApaI, and TaqI polymorphisms and osteoporosis risk: a meta-analysis
|
Yadav, Upendra
|
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21 |
1 |
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artikel
|
| 73 |
What should be the focus of counseling in parental consanguinity: genetic disorders or underlying beliefs
|
Soheilirad, Zahra
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21 |
1 |
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artikel
|
| 74 |
Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
|
Gholipoorfeshkecheh, Rahim
|
|
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21 |
1 |
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artikel
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