| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A modified protocol for highly efficient EBV-mediated immortalization of human B lymphocytes from small volumes of peripheral blood serum
|
Lemskaya, Natalya A.
|
|
2018
|
19 |
3 |
p. 221-223
|
artikel
|
| 2 |
A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia
|
Özkan, Didem Torun
|
|
2018
|
19 |
3 |
p. 271-272
|
artikel
|
| 3 |
Association of interleukin-6 and its -174G/C promoter polymorphism with clinical and laboratory characteristics of non hepatitis C virus rheumatoid arthritis patients
|
Raafat Hamed, Reham Mohamed
|
|
2018
|
19 |
3 |
p. 235-240
|
artikel
|
| 4 |
Association of nonalcoholic fatty liver disease grades with the plasma cell antigen-1 (PC-1) gene polymorphism
|
Borai, Ibrahim H.
|
|
2018
|
19 |
3 |
p. 241-246
|
artikel
|
| 5 |
Association of proinflammatory cytokine IL-20 gene polymorphism with psoriasis in north Indian population
|
Wani, Aadil
|
|
2018
|
19 |
3 |
p. 201-205
|
artikel
|
| 6 |
Association of P2X7 gene common polymorphisms with pulmonary tuberculosis in Lur population of Iran
|
Amiri, Ali
|
|
2018
|
19 |
3 |
p. 231-234
|
artikel
|
| 7 |
Association of toll-like receptor 2 polymorphisms with susceptibility to pulmonary tuberculosis in Sudanese
|
Zaki, H.
|
|
2018
|
19 |
3 |
p. 261-265
|
artikel
|
| 8 |
Association of variable number tandem repeats polymorphism in the IL-4 gene with end-stage renal disease in children
|
Elghoroury, Eman A.
|
|
2018
|
19 |
3 |
p. 191-195
|
artikel
|
| 9 |
Autism and KIR genes of the human genome: A brief meta-analysis
|
Pirzadroozbahani, Najmeh
|
|
2018
|
19 |
3 |
p. 159-164
|
artikel
|
| 10 |
Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration
|
Md Bakri, Norshakimah
|
|
2018
|
19 |
3 |
p. 207-213
|
artikel
|
| 11 |
Determinants and modifiers of bleeding phenotypes in haemophilia-A: General and tropical perspectives
|
Ibrahim, Umma A.
|
|
2018
|
19 |
3 |
p. 171-178
|
artikel
|
| 12 |
Editorial Board
|
|
|
2018
|
19 |
3 |
p. iii
|
artikel
|
| 13 |
Evaluation of dysmorphic children according to echocardiographic findings: A single center experience
|
Elmas, Muhsin
|
|
2018
|
19 |
3 |
p. 267-270
|
artikel
|
| 14 |
Evaluation of the association of single nucleotide polymorphisms in DDP4 and CDK5RAP2 genes with rheumatoid arthritis susceptibility in Iranian population
|
Malekshahi, Zahra
|
|
2018
|
19 |
3 |
p. 185-189
|
artikel
|
| 15 |
Expression study of CYP19A1 gene in a cohort of Iranian leiomyoma patients
|
Emrahi, Leila
|
|
2018
|
19 |
3 |
p. 197-200
|
artikel
|
| 16 |
Genotyping of PPAR-γ gene polymorphism in Egyptian neonates affected with sepsis disease and its severity
|
Shawky, Rabah M.
|
|
2018
|
19 |
3 |
p. 215-220
|
artikel
|
| 17 |
Impact of cell death pathway genes Fas 21377AA and FasL 2844CC polymorphisms on the risk of developing non-small cell lung cancer
|
Ezzeldin, Nada
|
|
2018
|
19 |
3 |
p. 179-183
|
artikel
|
| 18 |
Modified T-cells (using TCR and CTAs), chimeric antigen receptor (CAR) and other molecular tools in recent gene therapy
|
Odiba, A.S.
|
|
2018
|
19 |
3 |
p. 153-157
|
artikel
|
| 19 |
No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
|
Abtahi, Azadeh
|
|
2018
|
19 |
3 |
p. 247-251
|
artikel
|
| 20 |
Oncolytic virotherapy – A novel strategy for cancer therapy
|
Gopisankar, Mohanan Geetha
|
|
2018
|
19 |
3 |
p. 165-169
|
artikel
|
| 21 |
Risk factors of neural tube defects: A reality of Batna region in Algeria
|
Bourouba, Romyla
|
|
2018
|
19 |
3 |
p. 225-229
|
artikel
|
| 22 |
Yield of karyotyping in children with developmental delay and/or dysmorphic features in Sohag University Hospital, Upper Egypt
|
Sadek, Abdelrahim A.
|
|
2018
|
19 |
3 |
p. 253-259
|
artikel
|
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