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Best matches for next generation sequencing:

Next-Generation Sequencing RNA-Seq Library Construction. Podnar J et al. Curr Protoc Mol Biol. (2014)

Next-generation sequencing for research and diagnostics in kidney disease. Renkema KY et al. Nat Rev Nephrol. (2014)

Next-generation sequencing technologies: breaking the sound barrier of human genetics. Bahassi el M et al. Mutagenesis. (2014)

Search results

Items: 1 to 20 of 39067

1.

Comparison of molecular testing modalities for detection of ROS1 rearrangements in a cohort of positive patient samples.

Davies KD, Le AT, Sheren J, Nijmeh H, Gowan K, Jones KL, Varella-Garcia M, Aisner DL, Doebele RC.

J Thorac Oncol. 2018 Jun 20. pii: S1556-0864(18)30713-5. doi: 10.1016/j.jtho.2018.05.041. [Epub ahead of print]

PMID:
29935306
2.

Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterization.

Lu Y, Ren X, Wang Y, Bardai G, Sturm M, Dai Y, Riess O, Zhang Y, Li H, Li T, Zhai N, Zhang J, Rauch F, Han J.

Bone. 2018 Jun 20. pii: S8756-3282(18)30250-3. doi: 10.1016/j.bone.2018.06.018. [Epub ahead of print]

PMID:
29935254
3.

Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing.

Koczok K, Gombos É, Madar L, Török O, Balogh I.

Prenat Diagn. 2018 Jun 23. doi: 10.1002/pd.5319. [Epub ahead of print]

PMID:
29935118
4.

Genome wide analysis of meiotic recombination in yeast: For a few SNPs more.

Chakraborty P, Pankajam AV, Dutta A, Nishant KT.

IUBMB Life. 2018 Jun 22. doi: 10.1002/iub.1877. [Epub ahead of print] Review.

PMID:
29934971
5.

Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits.

Adriaens ME, Bezzina CR.

Biophys Rev. 2018 Jun 22. doi: 10.1007/s12551-018-0435-2. [Epub ahead of print] Review.

PMID:
29934864
6.

Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients.

Lu C, Li LX, Dong HL, Wei Q, Liu ZJ, Ni W, Gitler AD, Wu ZY.

J Mol Med (Berl). 2018 Jul;96(7):701-712. doi: 10.1007/s00109-018-1655-4. Epub 2018 Jun 11.

PMID:
29934652
7.

Expression ratio of the TGFβ-inducible gene MYO10 is prognostic for overall survival of squamous cell lung cancer patients and predicts chemotherapy response.

Dvornikov D, Schneider MA, Ohse S, Szczygieł M, Titkova I, Rosenblatt M, Muley T, Warth A, Herth FJ, Dienemann H, Thomas M, Timmer J, Schilling M, Busch H, Boerries M, Meister M, Klingmüller U.

Sci Rep. 2018 Jun 22;8(1):9517. doi: 10.1038/s41598-018-27912-1.

PMID:
29934580
8.

A Transposon Mutagenesis System for Bifidobacterium longum subsp. longum Based on an IS3 Family Insertion Sequence ISBlo11.

Sakanaka M, Nakakawaji S, Nakajima S, Fukiya S, Abe A, Saburi W, Mori H, Yokota A.

Appl Environ Microbiol. 2018 Jun 22. pii: AEM.00824-18. doi: 10.1128/AEM.00824-18. [Epub ahead of print]

PMID:
29934330
9.

[Development and application of polymorphic microsatellite markers in Saxifraga genus].

Yang W, Jiang W, Zhong GY, Liu NN, Chen Q, Wang XY.

Zhongguo Zhong Yao Za Zhi. 2018 May;43(10):2057-2066. doi: 10.19540/j.cnki.cjcmm.20180307.016. Chinese.

PMID:
29933671
10.
11.

Next-generation sequencing improves treatment efficacy and reduces hospitalization in children with drug-resistant epilepsy.

Peng J, Pang N, Wang Y, Wang XL, Chen J, Xiong J, Peng P, Zhu CH, Kessi MB, He F, Yin F.

CNS Neurosci Ther. 2018 Jun 22. doi: 10.1111/cns.12869. [Epub ahead of print]

PMID:
29933521
12.

Emergence of Integrase Resistance Mutations During Initial Therapy Containing Dolutegravir.

Fulcher JA, Du Y, Zhang TH, Sun R, Landovitz RJ.

Clin Infect Dis. 2018 Mar 21. doi: 10.1093/cid/ciy228. [Epub ahead of print]

PMID:
29933437
13.

SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequences.

Li Y, Wen S, Li D, Xie J, Wei X, Li X, Liu Y, Fang H, Yang Y, Lyu J.

Gene. 2018 Jun 19. pii: S0378-1119(18)30714-5. doi: 10.1016/j.gene.2018.06.058. [Epub ahead of print]

PMID:
29933018
14.

The first two mitochondrial genomes of the family Aphelinidae with novel gene orders and phylogenetic implications.

Zhu JC, Tang P, Zheng BY, Wu Q, Wei SJ, Chen XX.

Int J Biol Macromol. 2018 Jun 19. pii: S0141-8130(18)32200-1. doi: 10.1016/j.ijbiomac.2018.06.087. [Epub ahead of print]

PMID:
29932999
15.

Improving Single-Nucleotide Polymorphism-Based Fetal Fraction Estimation of Maternal Plasma Circulating Cell-Free DNA Using Bayesian Hierarchical Models.

Larson NB, Wang C, Na J, Rowsey RA, Highsmith WE, Hoppman NL, Kocher JP, Klee EW.

J Comput Biol. 2018 Jun 22. doi: 10.1089/cmb.2018.0056. [Epub ahead of print]

PMID:
29932737
16.

Assessing the efficiency of cultivation techniques to recover natural product biosynthetic gene populations from sediment.

Elfeki M, Alanjary M, Green SJ, Ziemert N, Murphy BT.

ACS Chem Biol. 2018 Jun 22. doi: 10.1021/acschembio.8b00254. [Epub ahead of print]

PMID:
29932624
17.

CSF3R mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia.

Zhang Y, Wang F, Chen X, Zhang Y, Wang M, Liu H, Cao P, Ma X, Wang T, Zhang J, Zhang X, Lu P, Liu H.

Cancer. 2018 Jun 22. doi: 10.1002/cncr.31586. [Epub ahead of print]

PMID:
29932212
18.

Understanding Intratumor Heterogeneity and Evolution in NSCLC and Potential New Therapeutic Approach.

Goto T, Hirotsu Y, Amemiya K, Mochizuki H, Omata M.

Cancers (Basel). 2018 Jun 22;10(7). pii: E212. doi: 10.3390/cancers10070212. Review.

PMID:
29932159
19.

Early colonisation and temporal dynamics of the gut microbial ecosystem in Standardbred foals.

Quercia S, Freccero F, Castagnetti C, Soverini M, Turroni S, Biagi E, Rampelli S, Lanci A, Mariella J, Chinellato E, Brigidi P, Candela M.

Equine Vet J. 2018 Jun 21. doi: 10.1111/evj.12983. [Epub ahead of print]

PMID:
29931762
20.

Appropriate nonmycorrhizal controls in arbuscular mycorrhiza research: a microbiome perspective.

Gryndler M, Šmilauer P, Püschel D, Bukovská P, Hršelová H, Hujslová M, Gryndlerová H, Beskid O, Konvalinková T, Jansa J.

Mycorrhiza. 2018 Jun 21. doi: 10.1007/s00572-018-0844-x. [Epub ahead of print]

PMID:
29931404

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