| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A brief review of exosomes and their roles in cancer
|
Mollaei, Homa
|
|
2017
|
11 |
C |
p. 70-74
|
artikel
|
| 2 |
A 10.43Mb duplication of chromosome region 5q31.2-q32 associated with a general delay in psychomotor development
|
Santoro, Eduardo
|
|
2017
|
11 |
C |
p. 169-171
|
artikel
|
| 3 |
Association between insulin receptor gene exon 17 rs1799817 variant and risk of nonalcoholic fatty liver disease
|
Mahmoudi, Touraj
|
|
2017
|
11 |
C |
p. 205-208
|
artikel
|
| 4 |
Association between rs11614913, rs3746444, rs2910164 and occurrence of breast cancer in Iranian population
|
Afsharzadeh, Seyed Morteza
|
|
2017
|
11 |
C |
p. 20-25
|
artikel
|
| 5 |
Association of genetic polymorphisms of the ABCG2, ABCB1, SLCO1B3 genes and the response to Imatinib in chronic myeloid leukemia patients with chronic phase
|
Nair, Devika
|
|
2017
|
11 |
C |
p. 14-19
|
artikel
|
| 6 |
Association of insulin-like growth factor-1 receptor polymorphism and insulin-like growth factor-1 plasma level with chronic immune thrombocytopenia in Chinese population
|
Liu, Liu
|
|
2017
|
11 |
C |
p. 1-4
|
artikel
|
| 7 |
Association of maternal angiotensinogen gene M235T polymorphism with preeclampsia in South India: A tertiary care hospital based case-control study
|
Chengalvala, Krishnaveni
|
|
2017
|
11 |
C |
p. 108-110
|
artikel
|
| 8 |
Association of mitochondrial DNA haplogroups with elite athletic status in Iranian population
|
Arjmand, Sareh
|
|
2017
|
11 |
C |
p. 81-84
|
artikel
|
| 9 |
Association of RANK/RANKL/OPG gene polymorphisms with risk of peripheral arterial disease (PAD) and critical limb ischemia in the general Italian population
|
Biscetti, Federico
|
|
2017
|
11 |
C |
p. 85-90
|
artikel
|
| 10 |
Association of vitamin D receptor and toll like receptor genetic variants and haplotypes with colon cancer risk: A case control study in Egypt
|
Ramadan, Ragaa A.
|
|
2017
|
11 |
C |
p. 209-216
|
artikel
|
| 11 |
Case report: Homozygous PRRT2 mutation in ICCA Egyptian family with reduced penetrance
|
Kishk, Nirmeen A.
|
|
2017
|
11 |
C |
p. 104-107
|
artikel
|
| 12 |
Clinical significance of TNFAIP3 rs2230926 T>G gene polymorphism in Egyptian cases with rheumatoid arthritis
|
Elkhawaga, Samy Y.
|
|
2017
|
11 |
C |
p. 58-63
|
artikel
|
| 13 |
Complete mitochondrial genome of Eurema blanda and phylogenetic relationship with its congener E. hecabe and other pierid butterflies
|
Yong, Hoi-Sen
|
|
2017
|
11 |
C |
p. 141-146
|
artikel
|
| 14 |
Computational analysis of nsSNPs of NPHS1 gene and their effect on protein structural stability
|
Joshi, Bhoomi B.
|
|
2017
|
11 |
C |
p. 98-103
|
artikel
|
| 15 |
Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in the human Quinone Oxidoreductase 1 (NQO1)
|
Singh, Hidam Bishworjit
|
|
2017
|
11 |
C |
p. 127-135
|
artikel
|
| 16 |
Corrigendum to "Mutation Analysis of Methylmalonyl COA Mutase Gene Exon 2 In Egyptian Families: Identification of 25 Novel Allelic Variants" [Meta Gene 3C (2015) 71–88]
|
Ghoraba, Dina A.
|
|
2017
|
11 |
C |
p. 136
|
artikel
|
| 17 |
CTNNA3 discordant regulation of nested LRRTM3, implications for autism spectrum disorder and Tourette syndrome
|
Fang, Zhiming
|
|
2017
|
11 |
C |
p. 43-48
|
artikel
|
| 18 |
CYP1A1 MspI polymorphism and cancer susceptibility among Latinos: A meta-analysis
|
Porchia, Leonardo M.
|
|
2017
|
11 |
C |
p. 197-204
|
artikel
|
| 19 |
Data mining and manual curation of published microarray datasets to establish a multi-gene panel for prediction of liver metastasis
|
Shah, Kanisha
|
|
2017
|
11 |
C |
p. 26-35
|
artikel
|
| 20 |
Detection of HER-2 gene copy number variations as a molecular marker in the peripheral blood of women with endometriosis in Iranian population: Case-control study
|
Hoseini, Maryam sadat
|
|
2017
|
11 |
C |
p. 164-168
|
artikel
|
| 21 |
Differential genetic background of primary and secondary tuberculosis in Russians
|
Garaeva, Anna F.
|
|
2017
|
11 |
C |
p. 178-180
|
artikel
|
| 22 |
Dimorphic association of dopaminergic transporter gene variants with treatment outcome: Pilot study in Indian ADHD probands
|
Ray, Anirban
|
|
2017
|
11 |
C |
p. 64-69
|
artikel
|
| 23 |
Editorial Board
|
|
|
2017
|
11 |
C |
p. i
|
artikel
|
| 24 |
Epidermal growth factor receptor (EGFR) in the era of Precision Medicine: The tale of a perfect example of targeted therapy. A review
|
Haddad, Joseph
|
|
2017
|
11 |
C |
p. 157-163
|
artikel
|
| 25 |
Familial GPC3 and GPC4-TFDP3 deletions at Xq26 associated with Simpson-Golabi-Behmel syndrome
|
DiMaio, Miriam S.
|
|
2017
|
11 |
C |
p. 147-151
|
artikel
|
| 26 |
Functional genetic polymorphisms in dopaminergic transporters: Association with ADHD traits in the Indian probands
|
Ghosh, Paramita
|
|
2017
|
11 |
C |
p. 117-122
|
artikel
|
| 27 |
Gene polymorphisms of desaturase enzymes of polyunsaturated fatty acid metabolism and adiponutrin and the increased risk of nonalcoholic fatty liver disease
|
Vernekar, Manvi
|
|
2017
|
11 |
C |
p. 152-156
|
artikel
|
| 28 |
Human NEIL1 DNA glycosylase: Structure, function and polymorphisms
|
Singh, Preety Kadian
|
|
2017
|
11 |
C |
p. 49-57
|
artikel
|
| 29 |
Investigating the link between MCP-1 A-2518G, RANTES G-403A, CX3CR1 V249I and MTHFR C677T gene polymorphisms and the risk of acute myocardial infarction among Egyptians
|
Hashad, Ingy M.
|
|
2017
|
11 |
C |
p. 181-188
|
artikel
|
| 30 |
Killer cell Immunoglobulin-like Receptors (KIRs) and hematopoietic stem cell transplantation outcomes. A review of the literature
|
Rammal, Rayan
|
|
2017
|
11 |
C |
p. 5-13
|
artikel
|
| 31 |
Meta-analysis reveals a lack of association between MRP2 C-24T genetic polymorphism and the pharmacokinetics of mycophenolic acid in adult renal transplant recipients
|
Liu, Kun
|
|
2017
|
11 |
C |
p. 91-97
|
artikel
|
| 32 |
Microbiota associated with Bactrocera carambolae and B. dorsalis (Insecta: Tephritidae) revealed by next-generation sequencing of 16S rRNA gene
|
Yong, Hoi-Sen
|
|
2017
|
11 |
C |
p. 189-196
|
artikel
|
| 33 |
Molecular analysis of exon 13 of cystic fibrosis patients in Middle East: High frequency of K710X mutation
|
Karimi, Nasibeh
|
|
2017
|
11 |
C |
p. 123-126
|
artikel
|
| 34 |
NOS3 gene Glu298Asp polymorphism and severity of disease in patients of ADPKD from North India
|
Pandita, Shewata
|
|
2017
|
11 |
C |
p. 75-80
|
artikel
|
| 35 |
Reference gene validation for relative quantification analysis of transcripts in urinary exfoliated cells among urothelial bladder carcinoma patients
|
Afsharpad, Mandana
|
|
2017
|
11 |
C |
p. 36-42
|
artikel
|
| 36 |
Relationship between adenosine deaminase polymorphism (c.22G>A) and oxidative stress in sickle cell anemia
|
da Silva, Danilo Grünig Humberto
|
|
2017
|
11 |
C |
p. 172-177
|
artikel
|
| 37 |
The association of GSTM1 and GSTT1 deletion polymorphisms with lung cancer risk: Evidence from an updated meta-analysis
|
Malik, Saima Shakil
|
|
2017
|
11 |
C |
p. 111-116
|
artikel
|
| 38 |
Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient
|
Ergun, Mehmet Ali
|
|
2017
|
11 |
C |
p. 137-140
|
artikel
|
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