| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A clinical case of multiple primary cancers in a carrier of rare SDK2 and NOTCH2 gene mutations
|
Timoshkina, Nataliya N.
|
|
|
22 |
1 |
|
artikel
|
| 2 |
A genetic variant of the NAMPT gene rs4730153 as a risk factor for the metabolic syndrome in younger age: a single-centre pilot study in Yogyakarta, Indonesia
|
Puspasari, Anggelia
|
|
|
22 |
1 |
|
artikel
|
| 3 |
A hybrid systems biology and systems pharmacology investigation of Zingerone’s effects on reconstructed human epidermal tissues
|
Amjad, Elham
|
|
|
22 |
1 |
|
artikel
|
| 4 |
Analysis of human aldehyde dehydrogenases (ALDH) gene expression pattern in breast cancer tissue samples: rutin-copper complex inhibit the breast cancer cell proliferation
|
Pattar, Shridhar V.
|
|
|
22 |
1 |
|
artikel
|
| 5 |
Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients
|
Listyasari, Nurin Aisyiyah
|
|
|
22 |
1 |
|
artikel
|
| 6 |
An association study between FokI, BsmI, miR-146a, and miR-155 and Behcet’s disease in the Egyptian population
|
Emara, Mohamed M.
|
|
|
22 |
1 |
|
artikel
|
| 7 |
A note of thanks
|
Elsayed, Solaf
|
|
|
22 |
1 |
|
artikel
|
| 8 |
A novel mutation in MTM1 gene in newborn, resulting in centronuclear myopathy phenotype: a case report
|
Dudzik, Aleksandra
|
|
|
22 |
1 |
|
artikel
|
| 9 |
A retrospective study of cases diagnosed with cystic fibrosis at a single care center in Syria
|
Al-Baba, Raghad
|
|
|
22 |
1 |
|
artikel
|
| 10 |
Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern India
|
Kumar, Rohit
|
|
|
22 |
1 |
|
artikel
|
| 11 |
Association of ABCC8 and KCNJ11 gene variants with type 1 diabetes in south Indians
|
Reddy, Shilpa
|
|
|
22 |
1 |
|
artikel
|
| 12 |
Association of genetic variants with prostate cancer in Africa: a concise review
|
Acheampong, Emmanuel
|
|
|
22 |
1 |
|
artikel
|
| 13 |
Association study between asthma and single nucleotide polymorphisms of ORMDL3, GSDMB, and IL1RL1 genes in an Algerian population
|
Ziani, Mouna
|
|
|
22 |
1 |
|
artikel
|
| 14 |
Association study of the BDNF gene polymorphism (G196A) with overweight/obesity among women from Northwest of Iran
|
Honarmand, Haneieh
|
|
|
22 |
1 |
|
artikel
|
| 15 |
Automated detection of colon cancer using genomic signal processing
|
Naeem, Safaa M.
|
|
|
22 |
1 |
|
artikel
|
| 16 |
Can microRNA become next-generation tools in molecular diagnostics and therapeutics? A systematic review
|
Saini, Vandana
|
|
|
22 |
1 |
|
artikel
|
| 17 |
Case report: a de-novo 7p12.3 microduplication detected in an infant with perineal hamartoma and imperforate anus
|
Kocaaga, Ayca
|
|
|
22 |
1 |
|
artikel
|
| 18 |
Chanarin–Dorfman syndrome: clinical/genetic features and natural history in six Pakistani patients
|
Waheed, Nadia
|
|
|
22 |
1 |
|
artikel
|
| 19 |
Characterization of the SARS-CoV-2 coronavirus X4-like accessory protein
|
Durojaye, Olanrewaju Ayodeji
|
|
|
22 |
1 |
|
artikel
|
| 20 |
Classic Cornelia de Lange syndrome with variant of unknown significance detected in NIPBL gene mutation: a case report
|
Desai, Jay J.
|
|
|
22 |
1 |
|
artikel
|
| 21 |
Combined markers for predicting cognitive deficit in patients with Alzheimer’s disease
|
Hussen, Dalia Farouk
|
|
|
22 |
1 |
|
artikel
|
| 22 |
Computer-aided design of some quinazoline analogues as epidermal growth factor receptor inhibitors
|
Ibrahim, Muhammad Tukur
|
|
|
22 |
1 |
|
artikel
|
| 23 |
Computer-assisted evaluation of plant-derived β-secretase inhibitors in Alzheimer’s disease
|
Ullah, Md. Asad
|
|
|
22 |
1 |
|
artikel
|
| 24 |
Coronavirus disease 19 and risk of hyperglycemia among Iraqi patients
|
Ad’hiah, Ali H.
|
|
|
22 |
1 |
|
artikel
|
| 25 |
Correction to: Extended blood group profiles for Malays, Chinese, and Indians in Peninsular Malaysia
|
Hajar, Che Ghazali Norul
|
|
|
22 |
1 |
|
artikel
|
| 26 |
Deconstructing the molecular genetics behind the PINK1/Parkin axis in Parkinson’s disease using Drosophila melanogaster as a model organism
|
Ganesan, Suchita
|
|
|
22 |
1 |
|
artikel
|
| 27 |
Decreased vitamin D levels in children with primary mono-symptomatic nocturnal enuresis
|
El-Baz, Farida M.
|
|
|
22 |
1 |
|
artikel
|
| 28 |
Differential expression of viral pathogen-associated molecular pattern receptors mRNA in Egyptian chronic hepatitis C virus patients
|
Suef, Reda A.
|
|
|
22 |
1 |
|
artikel
|
| 29 |
Differential gene expression analysis of ankylosing spondylitis shows deregulation of the HLA-DRB, HLA-DQB, ITM2A, and CTLA4 genes
|
AlEjielat, Rowan
|
|
|
22 |
1 |
|
artikel
|
| 30 |
Dysregulation in growth arrest-specific 5 and metastasis-associated lung adenocarcinoma transcript 1 gene expression predicts diagnosis and renal fibrosis in systemic lupus erythematosus patients
|
El-Desoky, Manal M.
|
|
|
22 |
1 |
|
artikel
|
| 31 |
Dysregulation of CCAAT/enhancer binding protein-alpha (CEBPA) expression in the bone marrow of acute myeloid leukemia patients
|
Hassan, Naglaa M.
|
|
|
22 |
1 |
|
artikel
|
| 32 |
Effect of Ag nanoparticles on viability of MCF-7 and Vero cell lines and gene expression of apoptotic genes
|
Sangour, Maryam Hassan
|
|
|
22 |
1 |
|
artikel
|
| 33 |
Evaluation of circulating miRNAs and mRNAs expression patterns in autism spectrum disorder
|
Abdelrahman, Amany H.
|
|
|
22 |
1 |
|
artikel
|
| 34 |
Evaluation of the impact of adaptation of Klebsiella pneumoniae clinical isolates to benzalkonium chloride on biofilm formation
|
Elekhnawy, Engy A.
|
|
|
22 |
1 |
|
artikel
|
| 35 |
Genetic polymorphism of HLA-G gene (G*01:03, G*01:04, and G*01:05N) in Iraqi patients with inflammatory bowel disease (ulcerative colitis and Crohn’s disease)
|
Abdul-Hussein, Sarah S.
|
|
|
22 |
1 |
|
artikel
|
| 36 |
HLA-A gene knockout using CRISPR/Cas9 system toward overcoming transplantation concerns
|
Amiri, Farshid
|
|
|
22 |
1 |
|
artikel
|
| 37 |
HOTAIR expression and prognostic impact in acute myeloid leukemia patients
|
Saad, Rawda Ahmed Alaaeldin Ahmed Mohamed
|
|
|
22 |
1 |
|
artikel
|
| 38 |
Identification of satellited markers by microdissection and fluorescence in situ hybridization: a clinical case of isodicentric chromosome 22
|
Lemskaya, Natalya A.
|
|
|
22 |
1 |
|
artikel
|
| 39 |
Identification of the most potent acetylcholinesterase inhibitors from plants for possible treatment of Alzheimer’s disease: a computational approach
|
Sarkar, Bishajit
|
|
|
22 |
1 |
|
artikel
|
| 40 |
Impact of Cytochromes P450 3A4 and 2B6 gene polymorphisms on predisposition and prognosis of acute myeloid leukemia: an Egyptian case-control study
|
Botros, Shahira Kamal Anis
|
|
|
22 |
1 |
|
artikel
|
| 41 |
In silico investigations on curcuminoids from Curcuma longa as positive regulators of the Wnt/β-catenin signaling pathway in wound healing
|
Reshad, Riyan Al Islam
|
|
|
22 |
1 |
|
artikel
|
| 42 |
In silico prediction of HBD gene variants in the Iranian population
|
Moradi, Keivan
|
|
|
22 |
1 |
|
artikel
|
| 43 |
In silico studies of bioactive compounds from selected African plants with inhibitory activity against nitric oxide synthase and arginase implicated in asthma
|
Umar, Haruna Isiyaku
|
|
|
22 |
1 |
|
artikel
|
| 44 |
Insulin-like growth factor binding protein 1 DNA methylation in type 2 diabetes
|
Hafez, Sally M.
|
|
|
22 |
1 |
|
artikel
|
| 45 |
In vitro characterization of human bone marrow mesenchymal stem cell-derived motor neurons induced by epigenetic modifiers
|
Sanooghi, Davood
|
|
|
22 |
1 |
|
artikel
|
| 46 |
Ligand-based drug design and molecular docking simulation studies of some novel anticancer compounds on MALME-3M melanoma cell line
|
Umar, Abdullahi Bello
|
|
|
22 |
1 |
|
artikel
|
| 47 |
lincR-Ccr2-5′AS and THRIL as potential biomarkers of multiple sclerosis
|
Shaker, Olfat Gamil
|
|
|
22 |
1 |
|
artikel
|
| 48 |
MicroRNAs as the critical regulators of protein kinases in prostate and bladder cancers
|
Zangoue, Malihe
|
|
|
22 |
1 |
|
artikel
|
| 49 |
Molecular analysis of CFTR gene mutations among Iraqi cystic fibrosis patients
|
Abdul-Qadir, Asal Gailan
|
|
|
22 |
1 |
|
artikel
|
| 50 |
Molecular study of Pompe disease in Egyptian infants
|
Essawi, Mona
|
|
|
22 |
1 |
|
artikel
|
| 51 |
Momordica charantia nanoparticles promote mitochondria biogenesis in the pancreas of diabetic-induced rats: gene expression study
|
Elekofehinti, Olusola Olalekan
|
|
|
22 |
1 |
|
artikel
|
| 52 |
Mutational analysis of p53 gene in cervical cancer and useful polymorphic variants in exons 3 and 4
|
Gbadegesin, Michael A.
|
|
|
22 |
1 |
|
artikel
|
| 53 |
N- and O-glycan analysis for the detection of glycosylation disorders
|
Gouda, Amr Sobhi
|
|
|
22 |
1 |
|
artikel
|
| 54 |
Overexpression of lncRNA AFAP1-AS1 as a diagnostic biomarker in non-small cell lung cancer
|
Ghalib Ibrahim Alnajar, Sajjad
|
|
|
22 |
1 |
|
artikel
|
| 55 |
PERIOD3 gene P415A/H417R polymorphism-linked familial advanced sleep phase
|
Okechukwu, Chidiebere Emmanuel
|
|
|
22 |
1 |
|
artikel
|
| 56 |
Phenotypic and genetic evaluation of human monocyte-derived dendritic cells generated from whole blood for immunotherapy
|
Hussein, Yousri M.
|
|
|
22 |
1 |
|
artikel
|
| 57 |
PIM2 and NF-κβ gene expression in a sample of AML and ALL Egyptian patients and its relevance to response to treatment
|
Abed El Rahman, Shymaa Kamal El Din
|
|
|
22 |
1 |
|
artikel
|
| 58 |
Potential role of vitamin D receptor-related polymorphisms in bronchopulmonary dysplasia
|
Abuelhamd, Walaa Alsharany
|
|
|
22 |
1 |
|
artikel
|
| 59 |
Potential treatment for chronic myeloid leukemia using microRNA: in silico comparison between plants and human microRNAs in targeting BCR-ABL1 gene
|
Mohamad, Syarifah Faezah Syed
|
|
|
22 |
1 |
|
artikel
|
| 60 |
Prevalence of enterotoxin genes (SEA to SEE) and antibacterial resistant pattern of Staphylococcus aureus isolated from clinical specimens in Assiut city of Egypt
|
Baz, Ahmed A.
|
|
|
22 |
1 |
|
artikel
|
| 61 |
Professor Rabah Mohamed Shawky, 1943–2021
|
Elsayed, Solaf M.
|
|
|
22 |
1 |
|
artikel
|
| 62 |
Protein secondary structure prediction (PSSP) using different machine algorithms
|
Afify, Heba M.
|
|
|
22 |
1 |
|
artikel
|
| 63 |
Rare dosage abnormalities flanking the SHOX gene
|
Bunyan, David J.
|
|
|
22 |
1 |
|
artikel
|
| 64 |
Recent advances in pharmacological diversification of Src family kinase inhibitors
|
Negi, Preeya
|
|
|
22 |
1 |
|
artikel
|
| 65 |
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse
|
Agarwala, Swati
|
|
|
22 |
1 |
|
artikel
|
| 66 |
Role of engulfment and cell motility 1 (ELMO1) gene polymorphism in development of diabetic kidney disease
|
Omar, Thoria A.
|
|
|
22 |
1 |
|
artikel
|
| 67 |
Role of matrilin-1 (MATN1) polymorphism in class III skeletal malocclusion with mandibular prognathism in Deutero-Malay race: a case-control study
|
Laviana, Avi
|
|
|
22 |
1 |
|
artikel
|
| 68 |
rs2253310 and rs4946936 common variants of FOXO3 gene in octogenarians and cancer: a pilot study in north India
|
Tia, Neelam
|
|
|
22 |
1 |
|
artikel
|
| 69 |
RUNX1 gene expression in Egyptian acute myeloid leukemia patients: may it have therapeutic implications?
|
Said, Fadwa
|
|
|
22 |
1 |
|
artikel
|
| 70 |
SCGB3A1 gene DNA methylation status is associated with breast cancer in Egyptian female patients
|
Nomair, Azhar Mohamed
|
|
|
22 |
1 |
|
artikel
|
| 71 |
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
|
EL Bouchikhi, Ihssane
|
|
|
22 |
1 |
|
artikel
|
| 72 |
Screening of single nucleotide polymorphisms among fuchs’ endothelial corneal dystrophy subjects in Malaysia
|
Ng, Ker Hsin
|
|
|
22 |
1 |
|
artikel
|
| 73 |
Secondary findings from whole-exome sequencing data in families with familial combined hyperlipidemia (FCHL)
|
Zakeri, Mana
|
|
|
22 |
1 |
|
artikel
|
| 74 |
Serum estrogen and its soluble receptor levels in Egyptian patients with acute leukemia: case-control study
|
El-Kaream, Samir Ali Abd
|
|
|
22 |
1 |
|
artikel
|
| 75 |
Spectrum of clinical manifestation of methylmalonic acidemia and homocystinuria in a family of six siblings: novel combination of transcobalamin receptor defect (CD320) and cblC deficiency (MMACHC)
|
Waheed, Nadia
|
|
|
22 |
1 |
|
artikel
|
| 76 |
Spontaneous apoptosis and BCL2 gene expression as predictors of early death and short overall survival in acute leukemia patients: a prospective, case cohort study
|
Ebian, Huda F.
|
|
|
22 |
1 |
|
artikel
|
| 77 |
Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status
|
Salah, Mona
|
|
|
22 |
1 |
|
artikel
|
| 78 |
Susceptibility to the novel coronavirus disease (COVID-19) is associated with ABO and Rh blood groups: a case-control study from Afghanistan
|
Saify, Khyber
|
|
|
22 |
1 |
|
artikel
|
| 79 |
TaqI polymorphism of the VDR gene: aspects related to the clinical behavior of COVID-19 in Cuban patients
|
Peralta, Estela Morales
|
|
|
22 |
1 |
|
artikel
|
| 80 |
Telomeric repeat-containing ribonucleic acid (TERRA) expression in patients with idiopathic pulmonary fibrosis
|
El-Desoky, Manal M.
|
|
|
22 |
1 |
|
artikel
|
| 81 |
The association between MDR1 C3435T genetic polymorphism and the risk of multidrug-resistant epilepsy in Egyptian children
|
Elmagid, Dina Salama Abd
|
|
|
22 |
1 |
|
artikel
|
| 82 |
The association of apolipoprotein-E (APOE) gene polymorphisms with coronary artery disease: a systematic review and meta-analysis
|
Ashiq, Sana
|
|
|
22 |
1 |
|
artikel
|
| 83 |
The association of manganese superoxide dismutase gene polymorphism (Rs4880) with diabetic macular edema in a cohort of type 2 diabetic Egyptian patients
|
Abdou, Doaa M.
|
|
|
22 |
1 |
|
artikel
|
| 84 |
The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women
|
Alzaidi, Zahraa
|
|
|
22 |
1 |
|
artikel
|
| 85 |
The expression profile of circANKRD36 and ANKRD36 as diagnostic biomarkers of chronic kidney disease in patients with type 2 diabetes mellitus
|
Rashad, Nearmeen M.
|
|
|
22 |
1 |
|
artikel
|
| 86 |
The prognostic impact of Wilms tumor-1 polymorphism (rs16754) and human myeloid inhibitory C-type lectin-like receptor expression in cytogenetically normal-acute myeloid leukemia
|
Bedair, Hanan M.
|
|
|
22 |
1 |
|
artikel
|
| 87 |
The prospective prognostic value of the immune checkpoint BTLA expression in adult acute myeloid leukemia patients
|
Radwan, Sara M.
|
|
|
22 |
1 |
|
artikel
|
| 88 |
The role of glutathione S-transferase omega gene polymorphisms in childhood acute lymphoblastic leukemia: a case-control study
|
Yassa, Marianne E.
|
|
|
22 |
1 |
|
artikel
|
| 89 |
The study of sodium and potassium channel gene single-nucleotide variation significance in non-mechanical forms of epilepsy
|
Khamdiyeva, Ozada
|
|
|
22 |
1 |
|
artikel
|
| 90 |
Tumor necrosis factor induced protein 3 gene polymorphism and the susceptibility to chronic primary immune thrombocytopenia in Egyptian children: a case-control study
|
El-hady, Marwa Abd
|
|
|
22 |
1 |
|
artikel
|
| 91 |
Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate
|
Arias, Sergio
|
|
|
22 |
1 |
|
artikel
|
| 92 |
Vitamin D levels and vitamin D receptor genetic variants in Egyptian cardiovascular disease patients with and without diabetes
|
Eweida, Soad M.
|
|
|
22 |
1 |
|
artikel
|
Tijdschrift beschrijving