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                             32 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A methodical microarray design enables surveying of expression of a broader range of genes in Ciona intestinalis Matsumae, Hiromi
2013
519 1 p. 82-90
9 p.
artikel
2 A novel homozygous 10 nucleotide deletion in BBS10 causes Bardet–Biedl syndrome in a Pakistani family Agha, Zehra
2013
519 1 p. 177-181
5 p.
artikel
3 Association between GSTM1 polymorphism and DNA adduct concentration in the occupational workers exposed to PAHs: A meta-analysis Liu, Min
2013
519 1 p. 71-76
6 p.
artikel
4 Association between two genetic variants of CD226 gene and Cervical Squamous Cell Carcinoma: A case–control study Shi, Shaoqing
2013
519 1 p. 159-163
5 p.
artikel
5 Association of IL-12, IL-18 variants and serum IL-18 with bladder cancer susceptibility in North Indian population Jaiswal, Praveen Kumar
2013
519 1 p. 128-134
7 p.
artikel
6 Characterization of bovine MHC DRB3 diversity in Latin American Creole cattle breeds Giovambattista, Guillermo
2013
519 1 p. 150-158
9 p.
artikel
7 Characterization of novel HMW-GS in two diploid species of Eremopyrum Dai, Shoufen
2013
519 1 p. 55-59
5 p.
artikel
8 Combined analysis of polymorphism variants in hMTH1, hOGG1 and MUTYH genes on the risk of type 2 diabetes in the Chinese population Cao, Lili
2013
519 1 p. 50-54
5 p.
artikel
9 Comparative genomic analysis and evolution of family-B G protein-coupled receptors from six model insect species Li, Chengjun
2013
519 1 p. 1-12
12 p.
artikel
10 Dissecting the mechanisms responsible for the multiple insecticide resistance phenotype in Anopheles gambiae s.s., M form, from Vallée du Kou, Burkina Faso Kwiatkowska, Rachel M.
2013
519 1 p. 98-106
9 p.
artikel
11 Editorial Board 2013
519 1 p. iv-v
nvt p.
artikel
12 EGF +61A>G polymorphism and gastrointestinal cancer risk: A HuGE review and meta-analysis Piao, Ying
2013
519 1 p. 26-33
8 p.
artikel
13 Frequency of LCT-13910C/T and LCT-22018G/A single nucleotide polymorphisms associated with adult-type hypolactasia/lactase persistence among Israelis of different ethnic groups Raz, Maytal
2013
519 1 p. 67-70
4 p.
artikel
14 Genome-wide identification and divergent transcriptional expression of StAR-related lipid transfer (START) genes in teleosts Teng, Huajing
2013
519 1 p. 18-25
8 p.
artikel
15 Identification and in silico analysis of a novel troponin C like gene from Ruditapes philippinarum (Bivalvia: Veneridae) and its transcriptional response for calcium challenge Umasuthan, Navaneethaiyer
2013
519 1 p. 194-201
8 p.
artikel
16 Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? D'Angelo, Rosalia
2013
519 1 p. 202-207
6 p.
artikel
17 Identification of the first deletion–insertion involving the complete structure of GAA gene and part of CCDC40 gene mediated by an Alu element Amiñoso, Cinthia
2013
519 1 p. 169-172
4 p.
artikel
18 Identification, quantification, and evolutionary analysis of a novel isoform of MCM9 Jeffries, Elizabeth P.
2013
519 1 p. 41-49
9 p.
artikel
19 Insights into the evolution of gene organization and multidrug resistance from Klebsiella pneumoniae plasmid pKF3-140 Bai, Jie
2013
519 1 p. 60-66
7 p.
artikel
20 Involvement of a novel intronic microRNA in cross regulation of N-methyltransferase genes involved in caffeine biosynthesis in Coffea canephora Mohanan, Shibin
2013
519 1 p. 107-112
6 p.
artikel
21 MicroRNA profile analysis on duck feather follicle and skin with high-throughput sequencing technology Zhang, Li
2013
519 1 p. 77-81
5 p.
artikel
22 Phenotype and Micro-array characterization of duplication 11q22.1-q25 and review of the literature Ben-Abdallah-Bouhjar, Inesse
2013
519 1 p. 135-141
7 p.
artikel
23 Physical mapping and cloning of RAD56 Mathiasen, David P.
2013
519 1 p. 182-186
5 p.
artikel
24 Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization Chen, Chih-Ping
2013
519 1 p. 164-168
5 p.
artikel
25 Rhodopsin p.N78I dominant mutation causing sectorial retinitis pigmentosa in a pedigree with intrafamilial clinical heterogeneity Rivera-De la Parra, David
2013
519 1 p. 173-176
4 p.
artikel
26 Roadmap to determine the point mutations involved in cardiomyopathy disorder: A Bayesian approach Kumar, Ambuj
2013
519 1 p. 34-40
7 p.
artikel
27 Significant differences in genotoxicity induced by retrovirus integration in human T cells and induced pluripotent stem cells Zheng, Weiyan
2013
519 1 p. 142-149
8 p.
artikel
28 SPAR methods revealed high genetic diversity within populations and high gene flow of Vanda coerulea Griff ex Lindl (Blue Vanda), an endangered orchid species Manners, Viki
2013
519 1 p. 91-97
7 p.
artikel
29 The complete mitochondrial genome sequence and gene organization of the mud crab (Scylla paramamosain) with phylogenetic consideration Ma, Hongyu
2013
519 1 p. 120-127
8 p.
artikel
30 The polymorphism for endothelial nitric oxide synthase gene, the level of nitric oxide and the risk for pre-eclampsia: A meta-analysis Dai, Bingqin
2013
519 1 p. 187-193
7 p.
artikel
31 Variants in endothelial nitric oxide synthase (eNOS) gene in idiopathic infertile Brazilian men Bianco, Bianca
2013
519 1 p. 13-17
5 p.
artikel
32 Vertebrate codon bias indicates a highly GC-rich ancestral genome Nabiyouni, Maryam
2013
519 1 p. 113-119
7 p.
artikel
                             32 gevonden resultaten
 
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