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                             37 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Accumulation of slightly deleterious mutations in the mitochondrial genome: A hallmark of animal domestication Hughes, Austin L.
2013
515 1 p. 28-33
6 p.
artikel
2 A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy Atay, Zeynep
2013
515 1 p. 197-199
3 p.
artikel
3 A novel mutation in the myeloperoxidase gene in a Chinese female with complete myeloperoxidase deficiency: The role of nonsense-mediated mRNA decay Wang, Kaiyu
2013
515 1 p. 205-207
3 p.
artikel
4 A recombinase paralog from the hyperthermophilic crenarchaeon Sulfolobus solfataricus enhances SsoRadA ssDNA binding and strand displacement Graham V, William J.
2013
515 1 p. 128-139
12 p.
artikel
5 Association between IL13 gene polymorphisms and susceptibility to cancer: A meta-analysis Su, Tong
2013
515 1 p. 56-61
6 p.
artikel
6 Association between interleukin-10 promoter polymorphisms and endometriosis: A meta-analysis Fan, Wei
2013
515 1 p. 49-55
7 p.
artikel
7 Association between osteoporosis and polymorphisms of the bone Gla protein, estrogen receptor 1, collagen 1-A1 and calcitonin receptor genes in Turkish postmenopausal women Tural, Sengul
2013
515 1 p. 167-172
6 p.
artikel
8 Association of resistin gene polymorphisms with insulin resistance in Egyptian obese patients El-Shal, Amal S.
2013
515 1 p. 233-238
6 p.
artikel
9 Association of the variant rs2243421 of human DOC-2/DAB2 interactive protein gene (hDAB2IP) with gastric cancer in the Chinese Han population Xu, Song
2013
515 1 p. 200-204
5 p.
artikel
10 Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine Sutherland, H.G.
2013
515 1 p. 187-192
6 p.
artikel
11 Cloning and expression characterization of the serum transferrin gene in the Chinese black sleeper (Bostrichthys sinensis) Gao, Jing
2013
515 1 p. 89-98
10 p.
artikel
12 Common variant in FUT2 gene is associated with levels of vitamin B12 in Indian population Tanwar, Vinay Singh
2013
515 1 p. 224-228
5 p.
artikel
13 Corrigendum to “Lytic bone disease as the presenting feature of Philadelphia-positive, derivative chromosome 7 myelodysplasia progressing to acute myeloid leukaemia” [GENE 501 (2012) 219–221] Tucker, D.
2013
515 1 p. 239-
1 p.
artikel
14 Editorial Board 2013
515 1 p. iv-v
nvt p.
artikel
15 Effects of carbon-ion beam or X-ray irradiation on anti-apoptosis ΔNp73 expression in HeLa cells Di, Cui-Xia
2013
515 1 p. 208-213
6 p.
artikel
16 Evaluation of hypermethylation and expression pattern of GMR2, GMR5, GMR8, and GRIA3 in patients with schizophrenia Kordi-Tamandani, Dor Mohammad
2013
515 1 p. 163-166
4 p.
artikel
17 Genetic polymorphism of vitamin D receptor gene affects the phenotype of PCOS Zadeh-Vakili, Azita
2013
515 1 p. 193-196
4 p.
artikel
18 14-3-3ε Gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum Chang, Bo
2013
515 1 p. 173-180
8 p.
artikel
19 Human PSENEN and U2AF1L4 genes are concertedly regulated by a genuine bidirectional promoter Didych, D.A.
2013
515 1 p. 34-41
8 p.
artikel
20 Human TNFα-induced protein 3-interacting protein 1 (TNIP1) promoter activation is regulated by retinoic acid receptors Gurevich, Igor
2013
515 1 p. 42-48
7 p.
artikel
21 Identification of glyoxalase 1 polymorphisms associated with enzyme activity Peculis, Raitis
2013
515 1 p. 140-143
4 p.
artikel
22 Identification of the highly accumulated microRNA*s in Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) Shao, Chaogang
2013
515 1 p. 123-127
5 p.
artikel
23 Mapping and tissue mRNA expression analysis of the pig solute carrier 27A (SLC27A) multigene family Gallardo, D.
2013
515 1 p. 220-223
4 p.
artikel
24 Methionine sulfoxide reduction in ciliates: Characterization of the ready-to-use methionine sulfoxide-R-reductase genes in Euplotes Dobri, Nicoleta
2013
515 1 p. 110-116
7 p.
artikel
25 Methylenetetrahydrofolate reductase 677TT genotype might be associated with an increased lung cancer risk in Asians Liu, Zheng-Bing
2013
515 1 p. 214-219
6 p.
artikel
26 Molecular cloning and tissue distribution of the phosphotyrosine interaction domain containing 1 (PID1) gene in Tianfu goat Xu, Honggang
2013
515 1 p. 71-77
7 p.
artikel
27 Novel genes that mediate nuclear respiratory factor 1-regualted neurite outgrowth in neuroblastoma IMR-32 cells Tong, Chih-Wei
2013
515 1 p. 62-70
9 p.
artikel
28 Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet–Biedl syndrome Khan, Saadullah
2013
515 1 p. 84-88
5 p.
artikel
29 Plasmodium falciparum RuvB1 is an active DNA helicase and translocates in the 5′–3′ direction Ahmad, Moaz
2013
515 1 p. 99-109
11 p.
artikel
30 Recombinase-mediated cassette exchange (RMCE) — A rapidly-expanding toolbox for targeted genomic modifications Turan, Soeren
2013
515 1 p. 1-27
27 p.
artikel
31 SNP identification in FBXO32 gene and their associations with growth traits in cattle Wang, Ailan
2013
515 1 p. 181-186
6 p.
artikel
32 Spectrum of MECP2 gene mutations in a cohort of Indian patients with Rett syndrome: Report of two novel mutations Das, Dhanjit Kumar
2013
515 1 p. 78-83
6 p.
artikel
33 Spectrum of mutations in Lebanese patients with phenylalanine hydroxylase deficiency Karam, Pascale E.
2013
515 1 p. 117-122
6 p.
artikel
34 The expression of multiple myosin heavy chain genes during skeletal muscle development of torafugu Takifugu rubripes embryos and larvae Asaduzzaman, Md.
2013
515 1 p. 144-154
11 p.
artikel
35 The identification of dysfunctional crosstalk of pathways in Parkinson disease Diao, Hongyu
2013
515 1 p. 159-162
4 p.
artikel
36 The IL-17F sequence variant is associated with susceptibility to tuberculosis Peng, Rong
2013
515 1 p. 229-232
4 p.
artikel
37 The p.Arg86Gln change in GARP2 (glutamic acid-rich protein-2) is a common West African-related polymorphism Gibriel, Abdullah A.Y.
2013
515 1 p. 155-158
4 p.
artikel
                             37 gevonden resultaten
 
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