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2570 résultats
Page 67 sur 86

Sara Masachis et al.
FASTBAC-Seq: Functional Analysis of Toxin–Antitoxin Systems in Bacteria by Deep Sequencing
Methods in Enzymology 2018
doi: 10.1016/bs.mie.2018.08.033

Wei-Jia Zhang et al.
Complete genome sequence of Shewanella benthica DB21MT-2, an obligate piezophilic bacterium isolated from the deepest Mariana Trench sediment
Marine Genomics 2018, vol. 44
doi: 10.1016/j.margen.2018.09.001

Camille Marchet et al.
De novoclustering of long reads by gene from transcriptomics data
Nucleic Acids Research 2018, vol. 47, issue 1
doi: 10.1093/nar/gky834

L. Allach El Khattabi et al.
Performance of semiconductor sequencing platform for non‐invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting
Ultrasound in Obstetrics & Gynecology 2018, vol. 54, issue 2
doi: 10.1002/uog.20112

Kanchan Karmakar et al.
Transcriptomic Analysis With the Progress of Symbiosis in ‘Crack-Entry’ Legume Arachis hypogaea Highlights Its Contrast With ‘Infection Thread’ Adapted Legumes
Molecular Plant-Microbe Interactions 2018, vol. 32, issue 3
doi: 10.1094/mpmi-06-18-0174-r

Miguel M. Pinto et al.
Sarcomeric disorganization and nemaline bodies in muscle biopsies of patients with EXOSC3 ‐related type 1 pontocerebellar hypoplasia
Muscle & Nerve 2018
doi: 10.1002/mus.26305

Irene Jiménez et al.
Circulating tumor DNA analysis enables molecular characterization of pediatric renal tumors at diagnosis
International Journal of Cancer 2018, vol. 144, issue 1
doi: 10.1002/ijc.31620

L. Mondoulet et al.
Gata3 hypermethylation and Foxp3 hypomethylation are associated with sustained protection and bystander effect following epicutaneous immunotherapy in peanut‐sensitized mice
Allergy 2018, vol. 74, issue 1
doi: 10.1111/all.13479

Kaori Sakai et al.
Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo
Plant Methods 2018, vol. 14, issue 1
doi: 10.1186/s13007-018-0275-x

Maria-Teresa Dotti et al.
Discordant manifestations in Italian brothers with GNE myopathy
Journal of the Neurological Sciences 2018, vol. 386
doi: 10.1016/j.jns.2018.01.002

Jérôme Audoux et al.
DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition
Genome Biology 2017, vol. 18, issue 1
doi: 10.1186/s13059-017-1372-2

Gustave Djedatin et al.
DuplicationDetector , a light weight tool for duplication detection using NGS data
Current Plant Biology 2017, vol. 9-10
doi: 10.1016/j.cpb.2017.07.001

Florence Rufflé et al.
New chimeric RNAs in acute myeloid leukemia
F1000Research 2017, vol. 6
doi: 10.12688/f1000research.11352.1

Valentina Boeva et al.
Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries
Nature Genetics 2017, vol. 49, issue 9
doi: 10.1038/ng.3921

Stéphanie Guey et al.
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians
European Journal of Human Genetics 2017, vol. 25, issue 8
doi: 10.1038/ejhg.2017.92

Alain Meyer et al.
IFN-β-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis
Acta Neuropathologica 2017, vol. 134, issue 4
doi: 10.1007/s00401-017-1731-9

Pierre-Antoine Juge et al.
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis
European Respiratory Journal 2017, vol. 49, issue 5
doi: 10.1183/13993003.02314-2016

Kopylova E. et al.
Deciphering metatranscriptomic data.
Methods in molecular biology (Clifton, NJ), (2015) 1269:279-291.
doi: 10.1007/978-1-4939-2291-8_17

Prasad MK et al.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
J Med Genet. Epub 2015 Oct 26.
doi: 10.1136/jmedgenet-2015-103302

Crottès D.et al.
SIGMAR1 Regulates Membrane Electrical Activity in Response to Extracellular Matrix Stimulation to Drive Cancer Cell Invasiveness.
Cancer Res. 76(3):607-18.
doi: 10.1158/0008-5472.CAN-15-1465

Portal MM. et al.
TARDIS, a targeted RNA directional sequencing method for rare RNA discovery.
Nat Protoc. (2015) (12):1915-38.
doi: 10.1038/nprot.2015.120

Mirzaa GM et al.
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.
Lancet Neurol. (2015)
doi: 10.1016/S1474-4422(15)00278-1

Chevalier B et al.
miR-34/449 control apical actin network formation during multicilio genesis through small GTPase pathways.
Nat Commun. (2015)
doi: 10.1038/ncomms9386

Grünewald TGP. et al.
Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite.
Nature Genetics (2015)
doi: 10.1038/ng.3363

Vembar SS et al.
A. The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages.
Genome Biol. (2015)
doi: 10.1186/s13059-015-0771-5

Chen H et al.
Reinforcement of STAT3 activity reprogrammes human embryonic stem cells to naive-like pluripotency.
Nat Commun. (2015)
doi: 10.1038/ncomms8095

Saintamand A. et al.
Elucidation of IgH 3′ region regulatory role during class switch recombination via germline deletion.
Nat Commun. (2015) 6:7084.
doi: 10.1038/ncomms8084

Rodier G. et al.
The transcription factor E4F1 coordinates CHK1-dependent checkpoint and mitochondrial functions.
Cell Rep. (2015) 11:220-33
doi: doi.org/10.1016/j.celrep.2015.03.024

Zacarias-Cabeza,J. et al.
Transcription-Dependent Generation of a Specialized Chromatin Structure at the TCRbeta Locus.
J. Immunol. (2015) 194, 3432-3443.
doi: 10.4049/jimmunol.1400789

Vanhille L. et al.
(2015). High-throughput and quantitative assessment of enhancer activity in mammals by CapStarr-seq.
Nat Commun.
doi: 10.1038/ncomms7905

2570 résultats
Page 67 sur 86

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