| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alliance of matrix metalloproteinase-9 (MMP-9) promoter gene polymorphism with chronic and aggressive periodontitis in Indian population
|
Majumder, Poulami
|
|
2017
|
12 |
C |
p. 88-93
6 p.
|
artikel
|
| 2 |
An adaptation of particle swarm clustering applied in basal cell carcinoma, squamous cell carcinoma of the skin and actinic keratosis
|
Poswar, Fabiano de Oliveira
|
|
2017
|
12 |
C |
p. 72-77
6 p.
|
artikel
|
| 3 |
Analysis of consequences of non-synonymous SNPs of USP9Y gene in human using bioinformatics tools
|
Nailwal, Mili
|
|
2017
|
12 |
C |
p. 13-17
5 p.
|
artikel
|
| 4 |
Assessment of p53 mutations, expression and prognosis in bladder cancer patients from Jordan: Identification of novel deletion mutations in the DNA-binding domain
|
Bodoor, Khaldon
|
|
2017
|
12 |
C |
p. 33-42
10 p.
|
artikel
|
| 5 |
Association of ACACB gene polymorphism (rs2268388, G>A) with type 2 diabetes and end stage renal disease in Pakistani Punjabi population
|
Zain, Maryam
|
|
2017
|
12 |
C |
p. 109-112
4 p.
|
artikel
|
| 6 |
Associations of PPAR-γ, APM1 and APOC1 gene polymorphisms with metabolic syndrome in children: A case-control study
|
Wang, Kaifeng
|
|
2017
|
12 |
C |
p. 104-108
5 p.
|
artikel
|
| 7 |
Comparative transcriptome analysis of PBMC from HIV patients pre- and post-antiretroviral therapy
|
Zhao, Fang
|
|
2017
|
12 |
C |
p. 50-61
12 p.
|
artikel
|
| 8 |
Down regulation of DNA repair genes Lig4, Ku70, Ku80, XRCC3 in primary myelodysplastic syndromes
|
Joshi, Dolly
|
|
2017
|
12 |
C |
p. 78-82
5 p.
|
artikel
|
| 9 |
Editorial Board
|
|
|
2017
|
12 |
C |
p. i-
1 p.
|
artikel
|
| 10 |
Effect of Glutathione S-transferase mu 1 (GSTM1) gene polymorphism on chronic myeloid leukemia risk and Imatinib treatment response
|
Al-Achkar, Walid
|
|
2017
|
12 |
C |
p. 113-117
5 p.
|
artikel
|
| 11 |
Evaluation of nephroblastoma overexpressed gene, a transcriptional target of forkhead box protein O1 in type 2 diabetes mellitus
|
Said, Hebatallah
|
|
2017
|
12 |
C |
p. 62-67
6 p.
|
artikel
|
| 12 |
Genetics of myocardial infarction: The role of thrombosis-associated genes. A review article
|
Msheik, A.
|
|
2017
|
12 |
C |
p. 138-149
12 p.
|
artikel
|
| 13 |
Genetic variations in interleukin 6 rs1800795 polymorphism and the association with susceptibility to Hashimoto's thyroiditis
|
Erdogan, M
|
|
2017
|
12 |
C |
p. 1-3
3 p.
|
artikel
|
| 14 |
Human papillomavirus 16 as a risk factor for oral leukoplakia: A meta-analysis
|
Jiang Ying,
|
|
2017
|
12 |
C |
p. 43-46
4 p.
|
artikel
|
| 15 |
Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, Central India
|
Devendra, R
|
|
2017
|
12 |
C |
p. 130-133
4 p.
|
artikel
|
| 16 |
Identification of novel missense HEXB gene mutation in Iranian-child with juvenile Sandhoff disease
|
Ebrahimzadeh-Vesal, Reza
|
|
2017
|
12 |
C |
p. 83-87
5 p.
|
artikel
|
| 17 |
Impact of inducible co-stimulator gene polymorphisms on acute rejection in renal transplant recipients: An updated systematic review and meta-analysis
|
Liu, Kun
|
|
2017
|
12 |
C |
p. 118-124
7 p.
|
artikel
|
| 18 |
Interleukin-1β (IL-1β) -31C/T and -511T/C promoter single nucleotide polymorphism in colorectal cancer in ethnic Kashmiri population - a case control study
|
Banday, Mujeeb Zafar
|
|
2017
|
12 |
C |
p. 94-103
10 p.
|
artikel
|
| 19 |
Metagenomic approach to study the bacterial community in clinical and subclinical mastitis in buffalo
|
Patel, Reena J.
|
|
2017
|
12 |
C |
p. 4-12
9 p.
|
artikel
|
| 20 |
Ninjurin 1 gene asp110ala genetic variants as a susceptibility factor in nerve damage leprosy patients of India
|
Sundaramoorthy, Arun
|
|
2017
|
12 |
C |
p. 18-21
4 p.
|
artikel
|
| 21 |
Novel large deletion in an atypical Peutz-Jeghers patient
|
Esperón, P
|
|
2017
|
12 |
C |
p. 68-71
4 p.
|
artikel
|
| 22 |
Rapid detection of HLA-B*5701 allele by in-house developed tetra-primer amplification refractory mutation system PCR
|
Chavan, Yashwant
|
|
2017
|
12 |
C |
p. 150-153
4 p.
|
artikel
|
| 23 |
Relationship of apolipoprotein (APOE) ε4 gene polymorphism with the risk of ischemic stroke: A hospital based case-control study
|
Kumar, Amit
|
|
2017
|
12 |
C |
p. 154-158
5 p.
|
artikel
|
| 24 |
Study of urotensin-2 (T21M and S89N) gene polymorphisms in systemic sclerosis
|
Kamal, Asmaa
|
|
2017
|
12 |
C |
p. 125-129
5 p.
|
artikel
|
| 25 |
The influence of different calorie restriction protocols on serum pro-inflammatory cytokines, adipokines and IGF-I levels in female C57BL6 mice: Short term and long term diet effects
|
Dogan, Soner
|
|
2017
|
12 |
C |
p. 22-32
11 p.
|
artikel
|
| 26 |
Top SNPs from the phenome-wide association study catalog and the risk of varicose veins of lower extremities: A replication study
|
Shadrina, Alexandra
|
|
2017
|
12 |
C |
p. 47-49
3 p.
|
artikel
|
| 27 |
Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures
|
Niranjana Murthy, Ashitha S.
|
|
2017
|
12 |
C |
p. 134-137
4 p.
|
artikel
|
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